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Current Protein & Peptide Science

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ISSN (Print): 1389-2037
ISSN (Online): 1875-5550

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Review Article

Allergen-like Molecules from Parasites

Author(s): Ju Yeong Kim, Myung-Hee Yi and Tai-Soon Yong*

Volume 21, Issue 2, 2020

Page: [186 - 202] Pages: 17

DOI: 10.2174/1389203720666190708154300

Price: $65

Abstract

Parasite infections modulate immunologic responses, and the loss of parasite infections in the last two to three decades might explain the increased prevalence of allergic diseases in developed countries. However, parasites can enhance allergic responses. Parasites contain or release allergen-like molecules that induce the specific immunoglobulin, IgE, and trigger type-2 immune responses. Some parasites and their proteins, such as Anisakis and Echinococcus granulosus allergens, act as typical allergens. A number of IgE-binding proteins of various helminthic parasites are cross-reactive to other environmental allergens, which cause allergic symptoms or hamper accurate diagnosis of allergic diseases. The cross-reactivity is based on the fact that parasite proteins are structurally homologous to common environmental allergens. In addition, IgE-binding proteins of parasites might be useful for developing vaccines to prevent host re-infection. This review discusses the functions of the IgE-biding proteins of parasites.

Keywords: Allergen, Anisakis, Echinococcus granulosus, IgE-binding protein, parasite, helminths.

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Graphical Abstract

[1]
Allen, J.E.; Maizels, R.M. Diversity and dialogue in immunity to helminths. Nat. Rev. Immunol., 2011, 11(6), 375-388.
[http://dx.doi.org/10.1038/nri2992] [PMID: 21610741]
[2]
Min, D.Y.; Soh, C.T. Evaluation of specific IgE antibody in Clonorchis sinensis infection. Korean J. Parasitol., 1983, 21(1), 27-31.
[http://dx.doi.org/10.3347/kjp.1983.21.1.27] [PMID: 12902666]
[3]
Fitzsimmons, C.M.; Falcone, F.H.; Dunne, D.W. Helminth Allergens, Parasite-Specific IgE, and Its Protective Role in Human Immunity. Front. Immunol., 2014, 5, 61.
[http://dx.doi.org/10.3389/fimmu.2014.00061] [PMID: 24592267]
[4]
McSorley, H.J.; Maizels, R.M. Helminth infections and host immune regulation. Clin. Microbiol. Rev., 2012, 25(4), 585-608.
[http://dx.doi.org/10.1128/CMR.05040-11] [PMID: 23034321]
[5]
Johansson, S.G.; Hourihane, J.O.; Bousquet, J.; Bruijnzeel-Koomen, C.; Dreborg, S.; Haahtela, T.; Kowalski, M.L.; Mygind, N.; Ring, J.; van Cauwenberge, P.; van Hage-Hamsten, M.; Wüthrich, B. A revised nomenclature for allergy. An EAACI position statement from the EAACI nomenclature task force. Allergy, 2001, 56(9), 813-824.
[http://dx.doi.org/10.1034/j.1398-9995.2001.t01-1-00001.x] [PMID: 11551246]
[6]
Santiago, H.C.; Bennuru, S.; Ribeiro, J.M.; Nutman, T.B. Structural differences between human proteins and aero- and microbial allergens define allergenicity. PLoS One, 2012, 7(7)e40552
[http://dx.doi.org/10.1371/journal.pone.0040552] [PMID: 22815762]
[7]
Tyagi, N.; Farnell, E.J.; Fitzsimmons, C.M.; Ryan, S.; Tukahebwa, E.; Maizels, R.M.; Dunne, D.W.; Thornton, J.M.; Furnham, N. Comparisons of Allergenic and Metazoan Parasite Proteins: Allergy the Price of Immunity. PLOS Comput. Biol., 2015, 11(10)e1004546
[http://dx.doi.org/10.1371/journal.pcbi.1004546] [PMID: 26513360]
[8]
Llorens, C.; Arcos, S.C.; Robertson, L.; Ramos, R.; Futami, R.; Soriano, B.; Ciordia, S.; Careche, M.; González-Muñoz, M.; Jiménez-Ruiz, Y.; Carballeda-Sangiao, N.; Moneo, I.; Albar, J.P.; Blaxter, M.; Navas, A. Functional insights into the infective larval stage of Anisakis simplex s.s., Anisakis pegreffii and their hybrids based on gene expression patterns. BMC Genomics, 2018, 19(1), 592.
[http://dx.doi.org/10.1186/s12864-018-4970-9] [PMID: 30086708]
[9]
Bielory, B.P.; Mainardi, T.; Rottem, M. Evolutionary immune response to conserved domains in parasites and aeroallergens. Allergy Asthma Proc., 2013, 34(1), 93-102.
[http://dx.doi.org/10.2500/aap.2013.34.3616] [PMID: 23406942]
[10]
Bach, J.F. The effect of infections on susceptibility to autoimmune and allergic diseases. N. Engl. J. Med., 2002, 347(12), 911-920.
[http://dx.doi.org/10.1056/NEJMra020100] [PMID: 12239261]
[11]
Pearce, N.; Aït-Khaled, N.; Beasley, R.; Mallol, J.; Keil, U.; Mitchell, E.; Robertson, C. Worldwide trends in the prevalence of asthma symptoms: phase III of the International Study of Asthma and Allergies in Childhood (ISAAC). Thorax, 2007, 62(9), 758-766.
[http://dx.doi.org/10.1136/thx.2006.070169] [PMID: 17504817]
[12]
Fallon, P.G.; Mangan, N.E. Suppression of TH2-type allergic reactions by helminth infection. Nat. Rev. Immunol., 2007, 7(3), 220-230.
[http://dx.doi.org/10.1038/nri2039] [PMID: 17318233]
[13]
van den Biggelaar, A.H.; van Ree, R.; Rodrigues, L.C.; Lell, B.; Deelder, A.M.; Kremsner, P.G.; Yazdanbakhsh, M. Decreased atopy in children infected with Schistosoma haematobium: a role for parasite-induced interleukin-10. Lancet, 2000, 356(9243), 1723-1727.
[http://dx.doi.org/10.1016/S0140-6736(00)03206-2] [PMID: 11095260]
[14]
Cooper, P.J.; Chico, M.E.; Rodrigues, L.C.; Ordonez, M.; Strachan, D.; Griffin, G.E.; Nutman, T.B. Reduced risk of atopy among school-age children infected with geohelminth parasites in a rural area of the tropics. J. Allergy Clin. Immunol., 2003, 111(5), 995-1000.
[http://dx.doi.org/10.1067/mai.2003.1348] [PMID: 12743563]
[15]
Maizels, R.M. Infections and allergy - helminths, hygiene and host immune regulation. Curr. Opin. Immunol., 2005, 17(6), 656-661.
[http://dx.doi.org/10.1016/j.coi.2005.09.001] [PMID: 16202576]
[16]
Dagoye, D.; Bekele, Z.; Woldemichael, K.; Nida, H.; Yimam, M.; Hall, A.; Venn, A.J.; Britton, J.R.; Hubbard, R.; Lewis, S.A. Wheezing, allergy, and parasite infection in children in urban and rural Ethiopia. Am. J. Respir. Crit. Care Med., 2003, 167(10), 1369-1373.
[http://dx.doi.org/10.1164/rccm.200210-1204OC] [PMID: 12738598]
[17]
Flohr, C.; Tuyen, L.N.; Lewis, S.; Quinnell, R.; Minh, T.T.; Liem, H.T.; Campbell, J.; Pritchard, D.; Hien, T.T.; Farrar, J.; Williams, H.; Britton, J. Poor sanitation and helminth infection protect against skin sensitization in Vietnamese children: A cross-sectional study. J. Allergy Clin. Immunol., 2006, 118(6), 1305-1311.
[http://dx.doi.org/10.1016/j.jaci.2006.08.035] [PMID: 17157661]
[18]
Scrivener, S.; Yemaneberhan, H.; Zebenigus, M.; Tilahun, D.; Girma, S.; Ali, S.; McElroy, P.; Custovic, A.; Woodcock, A.; Pritchard, D.; Venn, A.; Britton, J. Independent effects of intestinal parasite infection and domestic allergen exposure on risk of wheeze in Ethiopia: a nested case-control study. Lancet, 2001, 358(9292), 1493-1499.
[http://dx.doi.org/10.1016/S0140-6736(01)06579-5] [PMID: 11705561]
[19]
Cooper, P.J.; Chico, M.E.; Bland, M.; Griffin, G.E.; Nutman, T.B. Allergic symptoms, atopy, and geohelminth infections in a rural area of Ecuador. Am. J. Respir. Crit. Care Med., 2003, 168(3), 313-317.
[http://dx.doi.org/10.1164/rccm.200211-1320OC] [PMID: 12714349]
[20]
Rodrigues, L.C.; Newcombe, P.J.; Cunha, S.S.; Alcantara-Neves, N.M.; Genser, B.; Cruz, A.A.; Simoes, S.M.; Fiaccone, R.; Amorim, L.; Cooper, P.J.; Barreto, M.L. Early infection with Trichuris trichiura and allergen skin test reactivity in later childhood. Clin. Exp. Allergy, 2008, 38(11), 1769-1777.
[http://dx.doi.org/10.1111/j.1365-2222.2008.03027.x] [PMID: 18547322]
[21]
Huang, S.L.; Tsai, P.F.; Yeh, Y.F. Negative association of Enterobius infestation with asthma and rhinitis in primary school children in Taipei. Clin. Exp. Allergy, 2002, 32(7), 1029-1032.
[http://dx.doi.org/10.1046/j.1365-2745.2002.01424.x] [PMID: 12100049]
[22]
Araujo, M.I.; Lopes, A.A.; Medeiros, M.; Cruz, A.A.; Sousa-Atta, L.; Solé, D.; Carvalho, E.M. Inverse association between skin response to aeroallergens and Schistosoma mansoni infection. Int. Arch. Allergy Immunol., 2000, 123(2), 145-148.
[http://dx.doi.org/10.1159/000024433] [PMID: 11060486]
[23]
Rujeni, N.; Nausch, N.; Bourke, C.D.; Midzi, N.; Mduluza, T.; Taylor, D.W.; Mutapi, F. Atopy is inversely related to schistosome infection intensity: a comparative study in Zimbabwean villages with distinct levels of Schistosoma haematobium infection. Int. Arch. Allergy Immunol., 2012, 158(3), 288-298.
[http://dx.doi.org/10.1159/000332949] [PMID: 22398631]
[24]
Araujo, M.I.; Hoppe, B.; Medeiros, M., Jr; Alcântara, L.; Almeida, M.C.; Schriefer, A.; Oliveira, R.R.; Kruschewsky, R.; Figueiredo, J.P.; Cruz, A.A.; Carvalho, E.M. Impaired T helper 2 response to aeroallergen in helminth-infected patients with asthma. J. Infect. Dis., 2004, 190(10), 1797-1803.
[http://dx.doi.org/10.1086/425017] [PMID: 15499536]
[25]
Metenou, S.; Dembele, B.; Konate, S.; Dolo, H.; Coulibaly, S.Y.; Coulibaly, Y.I.; Diallo, A.A.; Soumaoro, L.; Coulibaly, M.E.; Sanogo, D.; Doumbia, S.S.; Traoré, S.F.; Mahanty, S.; Klion, A.; Nutman, T.B. At homeostasis filarial infections have expanded adaptive T regulatory but not classical Th2 cells. J. Immunol., 2010, 184(9), 5375-5382.
[http://dx.doi.org/10.4049/jimmunol.0904067] [PMID: 20357251]
[26]
Wilson, M.S.; Taylor, M.D.; Balic, A.; Finney, C.A.; Lamb, J.R.; Maizels, R.M. Suppression of allergic airway inflammation by helminth-induced regulatory T cells. J. Exp. Med., 2005, 202(9), 1199-1212.
[http://dx.doi.org/10.1084/jem.20042572] [PMID: 16275759]
[27]
Maizels, R.M.; Yazdanbakhsh, M. Immune regulation by helminth parasites: cellular and molecular mechanisms. Nat. Rev. Immunol., 2003, 3(9), 733-744.
[http://dx.doi.org/10.1038/nri1183] [PMID: 12949497]
[28]
Babu, S.; Blauvelt, C.P.; Kumaraswami, V.; Nutman, T.B. Regulatory networks induced by live parasites impair both Th1 and Th2 pathways in patent lymphatic filariasis: implications for parasite persistence. J. Immunol., 2006, 176(5), 3248-3256.
[http://dx.doi.org/10.4049/jimmunol.176.5.3248] [PMID: 16493086]
[29]
Metenou, S.; Babu, S.; Nutman, T.B. Impact of filarial infections on coincident intracellular pathogens: Mycobacterium tuberculosis and Plasmodium falciparum. Curr. Opin. HIV AIDS, 2012, 7(3), 231-238.
[http://dx.doi.org/10.1097/COH.0b013e3283522c3d] [PMID: 22418448]
[30]
Metenou, S.; Dembélé, B.; Konate, S.; Dolo, H.; Coulibaly, S.Y.; Coulibaly, Y.I.; Diallo, A.A.; Soumaoro, L.; Coulibaly, M.E.; Sanogo, D.; Doumbia, S.S.; Wagner, M.; Traoré, S.F.; Klion, A.; Mahanty, S.; Nutman, T.B. Patent filarial infection modulates malaria-specific type 1 cytokine responses in an IL-10-dependent manner in a filaria/malaria-coinfected population. J. Immunol., 2009, 183(2), 916-924.
[http://dx.doi.org/10.4049/jimmunol.0900257] [PMID: 19561105]
[31]
Santiago, H.C.; Nutman, T.B. Human Helminths and Allergic Disease: The Hygiene Hypothesis and Beyond. Am. J. Trop. Med. Hyg., 2016, 95(4), 746-753.
[http://dx.doi.org/10.4269/ajtmh.16-0348] [PMID: 27573628]
[32]
Alshishtawy, M.M.; Abdella, A.M.; Gelber, L.E.; Chapman, M.D. Asthma in Tanta, Egypt: serologic analysis of total and specific IgE antibody levels and their relationship to parasite infection. Int. Arch. Allergy Appl. Immunol., 1991, 96(4), 348-354.
[http://dx.doi.org/10.1159/000235520] [PMID: 1809691]
[33]
Buijs, J.; Borsboom, G.; Renting, M.; Hilgersom, W.J.; van Wieringen, J.C.; Jansen, G.; Neijens, J. Relationship between allergic manifestations and Toxocara seropositivity: a cross-sectional study among elementary school children. Eur. Respir. J., 1997, 10(7), 1467-1475.
[http://dx.doi.org/10.1183/09031936.97.10071467] [PMID: 9230232]
[34]
Choi, M.H.; Chang, Y.S.; Lim, M.K.; Bae, Y.M.; Hong, S.T.; Oh, J.K.; Yun, E.H.; Bae, M.J.; Kwon, H.S.; Lee, S.M.; Park, H.W.; Min, K.U.; Kim, Y.Y.; Cho, S.H. Clonorchis sinensis infection is positively associated with atopy in endemic area. Clin. Exp. Allergy, 2011, 41(5), 697-705.
[http://dx.doi.org/10.1111/j.1365-2222.2011.03746.x] [PMID: 21488996]
[35]
Dold, S.; Heinrich, J.; Wichmann, H.E.; Wjst, M. Ascaris-specific IgE and allergic sensitization in a cohort of school children in the former East Germany. J. Allergy Clin. Immunol., 1998, 102(3), 414-420.
[http://dx.doi.org/10.1016/S0091-6749(98)70129-0] [PMID: 9768582]
[36]
Hunninghake, G.M.; Soto-Quiros, M.E.; Avila, L.; Ly, N.P.; Liang, C.; Sylvia, J.S.; Klanderman, B.J.; Silverman, E.K.; Celedón, J.C. Sensitization to Ascaris lumbricoides and severity of childhood asthma in Costa Rica. J. Allergy Clin. Immunol., 2007, 119(3), 654-661.
[http://dx.doi.org/10.1016/j.jaci.2006.12.609] [PMID: 17336615]
[37]
Obihara, C.C.; Beyers, N.; Gie, R.P.; Hoekstra, M.O.; Fincham, J.E.; Marais, B.J.; Lombard, C.J.; Dini, L.A.; Kimpen, J.L. Respiratory atopic disease, Ascaris-immunoglobulin E and tuberculin testing in urban South African children. Clin. Exp. Allergy, 2006, 36(5), 640-648.
[http://dx.doi.org/10.1111/j.1365-2222.2006.02479.x] [PMID: 16650050]
[38]
Anthony, R.M.; Rutitzky, L.I.; Urban, J.F., Jr; Stadecker, M.J.; Gause, W.C. Protective immune mechanisms in helminth infection. Nat. Rev. Immunol., 2007, 7(12), 975-987.
[http://dx.doi.org/10.1038/nri2199] [PMID: 18007680]
[39]
Turner, K.J.; Feddema, L.; Quinn, E.H. Non-specific potentiation of IgE by parasitic infections in man. Int. Arch. Allergy Appl. Immunol., 1979, 58(2), 232-236.
[http://dx.doi.org/10.1159/000232197] [PMID: 370030]
[40]
Orr, T.S.; Riley, P.; Doe, J.E. Potentiated reagin response to egg albumin in Nippostrongylus brasiliensis infected rats. II. Time course of the reagin response. Immunology, 1971, 20(2), 185-189.
[PMID: 5102245]
[41]
Jarrett, E.; Bazin, H. Elevation of total serum IgE in rats following helminth parasite infection. Nature, 1974, 251(5476), 613-614.
[http://dx.doi.org/10.1038/251613a0] [PMID: 4547380]
[42]
Urban, J.F. Jr Cellular basis of the non-specific potentiation of the immunoglobulin E response after helminth parasite infection. Vet. Parasitol., 1982, 10(2-3), 131-140.
[http://dx.doi.org/10.1016/0304-4017(82)90019-X] [PMID: 6982561]
[43]
Bush, R.K. Parasites and allergic disease: another piece of the puzzle. J. Allergy Clin. Immunol., 2012, 130(1), 257-258.
[http://dx.doi.org/10.1016/j.jaci.2012.04.012] [PMID: 22583929]
[44]
Caraballo, L.; Acevedo, N. Allergy in the tropics: the impact of cross-reactivity between mites and ascaris. Front. Biosci. (Elite Ed.), 2011, 3, 51-64.
[http://dx.doi.org/10.2741/e219] [PMID: 21196284]
[45]
Fitzsimmons, C.M.; Dunne, D.W. Survival of the fittest: allergology or parasitology? Trends Parasitol., 2009, 25(10), 447-451.
[http://dx.doi.org/10.1016/j.pt.2009.07.004] [PMID: 19744885]
[46]
Santiago, H.da. C.; Nutman, T.B. Role in Allergic Diseases of Immunological Cross-Reactivity between Allergens and Homologues of Parasite Proteins. Crit. Rev. Immunol., 2016, 36(1), 1-11.
[http://dx.doi.org/10.1615/CritRevImmunol.2016016545] [PMID: 27480900]
[47]
Acevedo, N.; Sánchez, J.; Erler, A.; Mercado, D.; Briza, P.; Kennedy, M.; Fernandez, A.; Gutierrez, M.; Chua, K.Y.; Cheong, N.; Jiménez, S.; Puerta, L.; Caraballo, L. IgE cross-reactivity between Ascaris and domestic mite allergens: the role of tropomyosin and the nematode polyprotein ABA-1. Allergy, 2009, 64(11), 1635-1643.
[http://dx.doi.org/10.1111/j.1398-9995.2009.02084.x] [PMID: 19624559]
[48]
Mari, A.; Rasi, C.; Palazzo, P.; Scala, E. Allergen databases: current status and perspectives. Curr. Allergy Asthma Rep., 2009, 9(5), 376-383.
[http://dx.doi.org/10.1007/s11882-009-0055-9] [PMID: 19671381]
[49]
Minciullo, P.L.; Cascio, A.; Gangemi, S. Association between urticaria and nematode infections. Allergy Asthma Proc., 2018, 39(2), 86-95.
[http://dx.doi.org/10.2500/aap.2018.38.4104] [PMID: 29490766]
[50]
Kolkhir, P.; Balakirski, G.; Merk, H.F.; Olisova, O.; Maurer, M. Chronic spontaneous urticaria and internal parasites--a systematic review. Allergy, 2016, 71(3), 308-322.
[http://dx.doi.org/10.1111/all.12818] [PMID: 26648083]
[51]
Diemert, D.J.; Pinto, A.G.; Freire, J.; Jariwala, A.; Santiago, H.; Hamilton, R.G.; Periago, M.V.; Loukas, A.; Tribolet, L.; Mulvenna, J.; Correa-Oliveira, R.; Hotez, P.J.; Bethony, J.M. Generalized urticaria induced by the Na-ASP-2 hookworm vaccine: implications for the development of vaccines against helminths. J. Allergy Clin. Immunol., 2012, 130(1), 169-76.e6.
[http://dx.doi.org/10.1016/j.jaci.2012.04.027] [PMID: 22633322]
[52]
Scientific Opinion on risk assessment of parasites in fishery products. EFSA J., 2010, 8, 1543.
[http://dx.doi.org/10.2903/j.efsa.2010.1543]
[53]
Bao, M.; Pierce, G.J.; Pascual, S.; González-Muñoz, M.; Mattiucci, S.; Mladineo, I.; Cipriani, P.; Bušelić, I.; Strachan, N.J. Assessing the risk of an emerging zoonosis of worldwide concern: anisakiasis. Sci. Rep., 2017, 7, 43699.
[http://dx.doi.org/10.1038/srep43699] [PMID: 28287609]
[54]
Gregori, M.; Roura, Á.; Abollo, E.; González, A.F.; Pascual, S. Anisakis simplex complex (Nematoda: Anisakidae) in zooplankton communities from temperate NE Atlantic waters. J. Nat. Hist., 2015, 49, 755-773.
[http://dx.doi.org/10.1080/00222933.2014.979260]
[55]
Kirstein, F.; Horsnell, W.G.; Nieuwenhuizen, N.; Ryffel, B.; Lopata, A.L.; Brombacher, F. Anisakis pegreffii-induced airway hyperresponsiveness is mediated by gamma interferon in the absence of interleukin-4 receptor alpha responsiveness. Infect. Immun., 2010, 78(9), 4077-4086.
[http://dx.doi.org/10.1128/IAI.01131-09] [PMID: 20605987]
[56]
Umehara, A.; Kawakami, Y.; Araki, J.; Uchida, A. Molecular identification of the etiological agent of the human anisakiasis in Japan. Parasitol. Int., 2007, 56(3), 211-215.
[http://dx.doi.org/10.1016/j.parint.2007.02.005] [PMID: 17428725]
[57]
Audicana, M.T.; Kennedy, M.W. Anisakis simplex: from obscure infectious worm to inducer of immune hypersensitivity. Clin. Microbiol. Rev., 2008, 21(2), 360-379.
[http://dx.doi.org/10.1128/CMR.00012-07] [PMID: 18400801]
[58]
Daschner, A.; Cuéllar, C.; Sánchez-Pastor, S.; Pascual, C.Y.; Martín-Esteban, M. Gastro-allergic anisakiasis as a consequence of simultaneous primary and secondary immune response. Parasite Immunol., 2002, 24(5), 243-251.
[http://dx.doi.org/10.1046/j.1365-3024.2002.00458.x] [PMID: 12060318]
[59]
Nieuwenhuizen, N.E.; Lopata, A.L. Allergic reactions to Anisakis found in fish. Curr. Allergy Asthma Rep., 2014, 14(8), 455.
[http://dx.doi.org/10.1007/s11882-014-0455-3] [PMID: 25039016]
[60]
Nieuwenhuizen, N.E. Anisakis - immunology of a foodborne parasitosis. Parasite Immunol., 2016, 38(9), 548-557.
[http://dx.doi.org/10.1111/pim.12349] [PMID: 27428817]
[61]
Mazzucco, W.; Raia, D.D.; Marotta, C.; Costa, A.; Ferrantelli, V.; Vitale, F.; Casuccio, A. Anisakis sensitization in different population groups and public health impact: A systematic review. PLoS One, 2018, 13(9)e0203671
[http://dx.doi.org/10.1371/journal.pone.0203671] [PMID: 30235242]
[62]
Añíbarro, B.; Seoane, F.J.; Múgica, M.V. Involvement of hidden allergens in food allergic reactions. J. Investig. Allergol. Clin. Immunol., 2007, 17(3), 168-172.
[PMID: 17583104]
[63]
Choi, S.J.; Lee, J.C.; Kim, M.J.; Hur, G.Y.; Shin, S.Y.; Park, H.S. The clinical characteristics of Anisakis allergy in Korea. Korean J. Intern. Med. (Korean. Assoc. Intern. Med.), 2009, 24(2), 160-163.
[http://dx.doi.org/10.3904/kjim.2009.24.2.160] [PMID: 19543498]
[64]
Daschner, A.; Pascual, C.Y. Anisakis simplex: sensitization and clinical allergy. Curr. Opin. Allergy Clin. Immunol., 2005, 5(3), 281-285.
[http://dx.doi.org/10.1097/01.all.0000168795.12701.fd] [PMID: 15864089]
[65]
Daschner, A.; Vega de la Osada, F.; Pascual, C.Y. Allergy and parasites reevaluated: wide-scale induction of chronic urticaria by the ubiquitous fish-nematode Anisakis simplex in an endemic region. Allergol. Immunopathol. (Madr.), 2005, 33(1), 31-37.
[http://dx.doi.org/10.1157/13070606] [PMID: 15777521]
[66]
Ventura, M.T.; Napolitano, S.; Menga, R.; Cecere, R.; Asero, R. Anisakis simplex hypersensitivity is associated with chronic urticaria in endemic areas. Int. Arch. Allergy Immunol., 2013, 160(3), 297-300.
[http://dx.doi.org/10.1159/000339869] [PMID: 23095317]
[67]
Mazzucco, W.; Lacca, G.; Cusimano, R.; Provenzani, A.; Costa, A.; Di Noto, A.M.; Massenti, M.F.; Leto-Barone, M.S.; Lorenzo, G.D.; Vitale, F. Prevalence of sensitization to Anisakis simplex among professionally exposed populations in Sicily. Arch. Environ. Occup. Health, 2012, 67(2), 91-97.
[http://dx.doi.org/10.1080/19338244.2011.578683] [PMID: 22524649]
[68]
García-Palacios, L.; González, M.L.; Esteban, M.I.; Mirabent, E.; Perteguer, M.J.; Cuéllar, C. Enzyme-linked immunosorbent assay, immunoblot analysis and RAST fluoroimmunoassay analysis of serum responses against crude larval antigens of Anisakis simplex in a Spanish random population. J. Helminthol., 1996, 70(4), 281-289.
[http://dx.doi.org/10.1017/S0022149X0001556X] [PMID: 8960225]
[69]
Kimura, S.; Takagi, Y.; Gomi, K. IgE response to Anisakis compared to seafood. Allergy, 1999, 54(11), 1225-1226.
[http://dx.doi.org/10.1034/j.1398-9995.1999.00329.x] [PMID: 10604562]
[70]
Anisakis hypersensitivity in Italy: prevalence and clinical features: a multicenter study. Allergy, 2011, 66(12), 1563-1569.
[http://dx.doi.org/10.1111/j.1398-9995.2011.02691.x] [PMID: 21851362]
[71]
Abollo, E.; Paggi, L.; Pascual, S.; D’Amelio, S. Occurrence of recombinant genotypes of Anisakis simplex s.s. and Anisakis pegreffii (Nematoda: Anisakidae) in an area of sympatry. Infect. Genet. Evol., 2003, 3(3), 175-181.
[http://dx.doi.org/10.1016/S1567-1348(03)00073-X] [PMID: 14522181]
[72]
Mattiucci, S.; Nascetti, G. Molecular systematics, phylogeny and ecology of anisakid nematodes of the genus Anisakis Dujardin, 1845: an update. Parasite, 2006, 13(2), 99-113.
[http://dx.doi.org/10.1051/parasite/2006132099] [PMID: 16800118]
[73]
Moreno-Ancillo, A.; Caballero, M.T.; Cabañas, R.; Contreras, J.; Martin-Barroso, J.A.; Barranco, P.; López-Serrano, M.C. Allergic reactions to anisakis simplex parasitizing seafood. Ann. Allergy Asthma Immunol., 1997, 79(3), 246-250.
[http://dx.doi.org/10.1016/S1081-1206(10)63009-8] [PMID: 9305232]
[74]
Daschner, A.; Alonso-Gómez, A.; Cabañas, R.; Suarez-de-Parga, J.M.; López-Serrano, M.C. Gastroallergic anisakiasis: borderline between food allergy and parasitic disease-clinical and allergologic evaluation of 20 patients with confirmed acute parasitism by Anisakis simplex. J. Allergy Clin. Immunol., 2000, 105(1 Pt 1), 176-181.
[http://dx.doi.org/10.1016/S0091-6749(00)90194-5] [PMID: 10629469]
[75]
Nieuwenhuizen, N.E.; Lopata, A.L. Anisakis--a food-borne parasite that triggers allergic host defences. Int. J. Parasitol., 2013, 43(12-13), 1047-1057.
[http://dx.doi.org/10.1016/j.ijpara.2013.08.001] [PMID: 23994604]
[76]
Pravettoni, V.; Primavesi, L.; Piantanida, M. Anisakis simplex: current knowledge. Eur. Ann. Allergy Clin. Immunol., 2012, 44(4), 150-156.
[PMID: 23092000]
[77]
Moneo, I.; Caballero, M.L.; González-Muñoz, M.; Rodríguez-Mahillo, A.I.; Rodríguez-Perez, R.; Silva, A. Isolation of a heat-resistant allergen from the fish parasite Anisakis simplex. Parasitol. Res., 2005, 96(5), 285-289.
[http://dx.doi.org/10.1007/s00436-005-1362-2] [PMID: 15895253]
[78]
García, M.; Moneo, I.; Audicana, M.T.; del Pozo, M.D.; Muñoz, D.; Fernández, E.; Díez, J.; Etxenagusia, M.A.; Ansotegui, I.J.; Fernández de Corres, L. The use of IgE immunoblotting as a diagnostic tool in Anisakis simplex allergy. J. Allergy Clin. Immunol., 1997, 99(4), 497-501.
[http://dx.doi.org/10.1016/S0091-6749(97)70076-9] [PMID: 9111494]
[79]
Lorenzo, S.; Iglesias, R.; Leiro, J.; Ubeira, F.M.; Ansotegui, I.; García, M.; Fernández de Corres, L. Usefulness of currently available methods for the diagnosis of Anisakis simplex allergy. Allergy, 2000, 55(7), 627-633.
[http://dx.doi.org/10.1034/j.1398-9995.2000.00471.x] [PMID: 10921461]
[80]
Sastre, J.; Lluch-Bernal, M.; Quirce, S.; Arrieta, I.; Lahoz, C.; Del Amo, A.; Fernández-Caldas, E.; Marañón, F. A double-blind, placebo-controlled oral challenge study with lyophilized larvae and antigen of the fish parasite, Anisakis simplex. Allergy, 2000, 55(6), 560-564.
[http://dx.doi.org/10.1034/j.1398-9995.2000.00422.x] [PMID: 10858988]
[81]
Miles, S.; Fordham, R.; Mills, C.; Valovirta, E.; Mugford, M. A framework for measuring costs to society of IgE-mediated food allergy. Allergy, 2005, 60(8), 996-1003.
[http://dx.doi.org/10.1111/j.1398-9995.2005.00868.x] [PMID: 15969679]
[82]
Arcos, S.C.; Ciordia, S.; Roberston, L.; Zapico, I.; Jiménez-Ruiz, Y.; Gonzalez-Muñoz, M.; Moneo, I.; Carballeda-Sangiao, N.; Rodriguez-Mahillo, A.; Albar, J.P.; Navas, A. Proteomic profiling and characterization of differential allergens in the nematodes Anisakis simplex sensu stricto and A. pegreffii. Proteomics, 2014, 14(12), 1547-1568.
[http://dx.doi.org/10.1002/pmic.201300529] [PMID: 24723494]
[83]
Baird, F.J.; Su, X.; Aibinu, I.; Nolan, M.J.; Sugiyama, H.; Otranto, D.; Lopata, A.L.; Cantacessi, C. The Anisakis transcriptome provides a resource for fundamental and applied studies on allergy-causing parasites. PLoS Negl. Trop. Dis., 2016, 10(7)e0004845
[http://dx.doi.org/10.1371/journal.pntd.0004845] [PMID: 27472517]
[84]
López, I.; Pardo, M.A. A phage display system for the identification of novel Anisakis simplex antigens. J. Immunol. Methods, 2011, 373(1-2), 247-251.
[http://dx.doi.org/10.1016/j.jim.2011.08.009] [PMID: 21893063]
[85]
Fæste, C.K.; Jonscher, K.R.; Dooper, M.M.; Egge-Jacobsen, W.; Moen, A.; Daschner, A.; Egaas, E.; Christians, U. Characterisation of potential novel allergens in the fish parasite Anisakis simplex. EuPA Open Proteom., 2014, 4, 140-155.
[http://dx.doi.org/10.1016/j.euprot.2014.06.006] [PMID: 27110489]
[86]
González-Fernández, J.; Daschner, A.; Nieuwenhuizen, N.E.; Lopata, A.L.; Frutos, C.D.; Valls, A.; Cuéllar, C. Haemoglobin, a new major allergen of Anisakis simplex. Int. J. Parasitol., 2015, 45(6), 399-407.
[http://dx.doi.org/10.1016/j.ijpara.2015.01.002] [PMID: 25683373]
[87]
Shimakura, K.; Miura, H.; Ikeda, K.; Ishizaki, S.; Nagashima, Y.; Shirai, T.; Kasuya, S.; Shiomi, K. Purification and molecular cloning of a major allergen from Anisakis simplex. Mol. Biochem. Parasitol., 2004, 135(1), 69-75.
[http://dx.doi.org/10.1016/j.molbiopara.2004.01.007] [PMID: 15287588]
[88]
Moneo, I.; Caballero, M.L.; Gómez, F.; Ortega, E.; Alonso, M.J. Isolation and characterization of a major allergen from the fish parasite Anisakis simplex. J. Allergy Clin. Immunol., 2000, 106(1 Pt 1), 177-182.
[http://dx.doi.org/10.1067/mai.2000.106732] [PMID: 10887322]
[89]
Gamboa, P.M.; Asturias, J.; Martínez, R.; Antépara, I.; Jáuregui, I.; Urrutia, I.; Fernández, J.; Sanz, M.L. Diagnostic utility of components in allergy to Anisakis simplex. J. Investig. Allergol. Clin. Immunol., 2012, 22(1), 13-19.
[PMID: 22448449]
[90]
Anadón, A.M.; Rodríguez, E.; Gárate, M.T.; Cuéllar, C.; Romarís, F.; Chivato, T.; Rodero, M.; González-Díaz, H.; Ubeira, F.M. Diagnosing human anisakiasis: recombinant Ani s 1 and Ani s 7 allergens versus the UniCAP 100 fluorescence enzyme immunoassay. Clin. Vaccine Immunol., 2010, 17(4), 496-502.
[http://dx.doi.org/10.1128/CVI.00443-09] [PMID: 20107002]
[91]
Pérez-Pérez, J.; Fernández-Caldas, E.; Marañón, F.; Sastre, J.; Bernal, M.L.; Rodríguez, J.; Bedate, C.A. Molecular cloning of paramyosin, a new allergen of Anisakis simplex. Int. Arch. Allergy Immunol., 2000, 123(2), 120-129.
[http://dx.doi.org/10.1159/000024442] [PMID: 11060483]
[92]
Tsai, L.C.; Peng, H.J.; Lee, C.S.; Chao, P.L.; Tang, R.B.; Tsai, J.J.; Shen, H.D.; Hung, M.W.; Han, S.H. Molecular cloning and characterization of full-length cDNAs encoding a novel high-molecular-weight Dermatophagoides pteronyssinus mite allergen, Der p 11. Allergy, 2005, 60(7), 927-937.
[http://dx.doi.org/10.1111/j.1398-9995.2005.00637.x] [PMID: 15932384]
[93]
Asturias, J.A.; Eraso, E.; Martínez, A. Cloning and high level expression in Escherichia coli of an Anisakis simplex tropomyosin isoform. Mol. Biochem. Parasitol., 2000, 108(2), 263-267.
[http://dx.doi.org/10.1016/S0166-6851(00)00218-8] [PMID: 10838230]
[94]
Jeong, K.Y.; Hong, C.S.; Yong, T.S. Allergenic tropomyosins and their cross-reactivities. Protein Pept. Lett., 2006, 13(8), 835-845.
[http://dx.doi.org/10.2174/092986606777841244] [PMID: 17073731]
[95]
Asturias, J.A.; Eraso, E.; Moneo, I.; Martínez, A. Is tropomyosin an allergen in Anisakis? Allergy, 2000, 55(9), 898-899.
[http://dx.doi.org/10.1034/j.1398-9995.2000.00734.x] [PMID: 11003461]
[96]
Guarneri, F.; Guarneri, C.; Benvenga, S. Cross-reactivity of Anisakis simplex: possible role of Ani s 2 and Ani s 3. Int. J. Dermatol., 2007, 46(2), 146-150.
[PMID: 17269964]
[97]
Rodríguez, E.; Anadón, A.M.; García-Bodas, E.; Romarís, F.; Iglesias, R.; Gárate, T.; Ubeira, F.M. Novel sequences and epitopes of diagnostic value derived from the Anisakis simplex Ani s 7 major allergen. Allergy, 2008, 63(2), 219-225.
[http://dx.doi.org/10.1111/j.1398-9995.2007.01564.x] [PMID: 18186812]
[98]
Anadón, A.M.; Romarís, F.; Escalante, M.; Rodríguez, E.; Gárate, T.; Cuéllar, C.; Ubeira, F.M. The Anisakis simplex Ani s 7 major allergen as an indicator of true Anisakis infections. Clin. Exp. Immunol., 2009, 156(3), 471-478.
[http://dx.doi.org/10.1111/j.1365-2249.2009.03919.x] [PMID: 19438600]
[99]
Cuéllar, C.; Daschner, A.; Valls, A.; De Frutos, C.; Fernández-Fígares, V.; Anadón, A.M.; Rodríguez, E.; Gárate, T.; Rodero, M.; Ubeira, F.M. Ani s 1 and Ani s 7 recombinant allergens are able to differentiate distinct Anisakis simplex-associated allergic clinical disorders. Arch. Dermatol. Res., 2012, 304(4), 283-288.
[http://dx.doi.org/10.1007/s00403-012-1206-8] [PMID: 22249742]
[100]
Kobayashi, Y.; Ohsaki, K.; Ikeda, K.; Kakemoto, S.; Ishizaki, S.; Shimakura, K.; Nagashima, Y.; Shiomi, K. Identification of novel three allergens from Anisakis simplex by chemiluminescent immunoscreening of an expression cDNA library. Parasitol. Int., 2011, 60(2), 144-150.
[http://dx.doi.org/10.1016/j.parint.2011.01.004] [PMID: 21262386]
[101]
Rodriguez-Mahillo, A.I.; Gonzalez-Muñoz, M.; Gomez-Aguado, F.; Rodriguez-Perez, R.; Corcuera, M.T.; Caballero, M.L.; Moneo, I. Cloning and characterisation of the Anisakis simplex allergen Ani s 4 as a cysteine-protease inhibitor. Int. J. Parasitol., 2007, 37(8-9), 907-917.
[http://dx.doi.org/10.1016/j.ijpara.2007.01.007] [PMID: 17324433]
[102]
Kobayashi, Y.; Ishizaki, S.; Shimakura, K.; Nagashima, Y.; Shiomi, K. Molecular cloning and expression of two new allergens from Anisakis simplex. Parasitol. Res., 2007, 100(6), 1233-1241.
[http://dx.doi.org/10.1007/s00436-006-0396-4] [PMID: 17180690]
[103]
Kobayashi, Y.; Shimakura, K.; Ishizaki, S.; Nagashima, Y.; Shiomi, K. Purification and cDNA cloning of a new heat-stable allergen from Anisakis simplex. Mol. Biochem. Parasitol., 2007, 155(2), 138-145.
[http://dx.doi.org/10.1016/j.molbiopara.2007.06.012] [PMID: 17689675]
[104]
Rodriguez-Perez, R.; Moneo, I.; Rodriguez-Mahillo, A.; Caballero, M.L. Cloning and expression of Ani s 9, a new Anisakis simplex allergen. Mol. Biochem. Parasitol., 2008, 159(2), 92-97.
[http://dx.doi.org/10.1016/j.molbiopara.2008.02.008] [PMID: 18378015]
[105]
Cho, M.K.; Park, M.K.; Kang, S.A.; Caballero, M.L.; Perez-Pinar, T.; Rodriguez-Perez, R.; Ock, M.S.; Cha, H.J.; Hong, Y.C.; Yu, H.S. Allergenicity of two Anisakis simplex allergens evaluated in vivo using an experimental mouse model. Exp. Parasitol., 2014, 146, 71-77.
[http://dx.doi.org/10.1016/j.exppara.2014.09.008] [PMID: 25300761]
[106]
Park, H.K.; Cho, M.K.; Park, M.K.; Kang, S.A.; Kim, Y.S.; Kim, K.U.; Lee, M.K.; Ock, M.S.; Cha, H.J.; Yu, H.S.A.A. 24 kDa excretory-secretory protein of Anisakis simplex larvae could elicit allergic airway inflammation in mice. Korean J. Parasitol., 2011, 49(4), 373-380.
[http://dx.doi.org/10.3347/kjp.2011.49.4.373] [PMID: 22355204]
[107]
Caballero, M.L.; Umpierrez, A.; Moneo, I.; Rodriguez-Perez, R. Ani s 10, a new Anisakis simplex allergen: cloning and heterologous expression. Parasitol. Int., 2011, 60(2), 209-212.
[http://dx.doi.org/10.1016/j.parint.2011.01.003] [PMID: 21310242]
[108]
Kobayashi, Y.; Kakemoto, S.; Shimakura, K.; Shiomi, K. Molecular cloning and expression of a new major allergen, Ani s 14, from Anisakis simplex. Shokuhin Eiseigaku Zasshi, 2015, 56(5), 194-199.
[http://dx.doi.org/10.3358/shokueishi.56.194] [PMID: 26537648]
[109]
Arrieta, I.; del Barrio, M.; Vidarte, L.; del Pozo, V.; Pastor, C.; Gonzalez-Cabrero, J.; Cárdaba, B.; Rojo, M.; Mínguez, A.; Cortegano, I.; Gallardo, S.; Aceituno, E.; Palomino, P.; Vivanco, F.; Lahoz, C. Molecular cloning and characterization of an IgE-reactive protein from Anisakis simplex: Ani s 1. Mol. Biochem. Parasitol., 2000, 107(2), 263-268.
[http://dx.doi.org/10.1016/S0166-6851(00)00192-4] [PMID: 10779602]
[110]
Rausch, R.L. Echinococcus granulosus: biology and ecology.Compendium on cystic echinococcosis; Andersen, F.L.; Ouhelli, H; Kachani, M., Ed.; Brigham Young University Print Services: Provo, UT, USA, 1997, pp. 18-53.
[111]
Kritikou-Pliota, E.; Galanakis, E.; Siamopoulou, A.; Lapatsanis, P.D. An unusual cause of mild urticaria. Lancet Infect. Dis., 2001, 1(1), 20.
[http://dx.doi.org/10.1016/S1473-3099(01)00017-2] [PMID: 11871405]
[112]
Veraldi, S.; Miadonna, A. Chronic “idiopathic” urticaria and hydatid disease. Allergy, 1998, 53(12), 1234-1235.
[http://dx.doi.org/10.1111/j.1398-9995.1998.tb03856.x] [PMID: 9930612]
[113]
Rosay, H.; Lançon, J.P.; Oeuvrard, C.; Bernard, A.; Caillard, B. [Peroperative bronchospasm during surgery of hydatid cysts Ann. Fr. Anesth. Reanim., 1988, 7(6), 509-510.
[http://dx.doi.org/10.1016/S0750-7658(88)80090-X] [PMID: 3223642]
[114]
Saenz de San Pedro, B.; Cazaña, J.L.; Cobo, J.; Serrano, C.L.; Quiralte, J.; Contreras, J.; Martinez, F. Anaphylactic shock by rupture of hydatid hepatic cyst. Follow-up by specific IgE serum antibodies. Allergy, 1992, 47(5), 568-570.
[http://dx.doi.org/10.1111/j.1398-9995.1992.tb00683.x] [PMID: 1485662]
[115]
Boyano, T.; Moldenhauer, F.; Mira, J.; Joral, A.; Saiz, F. Systemic anaphylaxis due to hepatic hydatid disease. J. Investig. Allergol. Clin. Immunol., 1994, 4(3), 158-159.
[PMID: 7981887]
[116]
Mooraki, A.; Rahbar, M.H.; Bastani, B. Spontaneous systemic anaphylaxis as an unusual presentation of hydatid cyst: report of two cases. Am. J. Trop. Med. Hyg., 1996, 55(3), 302-303.
[http://dx.doi.org/10.4269/ajtmh.1996.55.302] [PMID: 8842119]
[117]
Giulekas, D.; Papacosta, D.; Papaconstantinou, C.; Barbarousis, D.; Angel, J. Recurrent anaphylactic shock as a manifestation of echinococcosis. Report of a case. Scand. J. Thorac. Cardiovasc. Surg., 1986, 20(2), 175-177.
[http://dx.doi.org/10.3109/14017438609106498] [PMID: 3738450]
[118]
Stey, C.; Jost, R.; Ammann, R. [Recurrent, life-threatening anaphylaxis as initial manifestation of cystic echinococcosis (granulosus) of the liver Schweiz. Med. Wochenschr., 1993, 123(29), 1445-1447.
[PMID: 8367703]
[119]
Vuitton, D.A. Echinococcosis and allergy. Clin. Rev. Allergy Immunol., 2004, 26(2), 93-104.
[http://dx.doi.org/10.1007/s12016-004-0004-2] [PMID: 15146106]
[120]
Ortona, E.; Margutti, P.; Delunardo, F.; Vaccari, S.; Riganò, R.; Profumo, E.; Buttari, B.; Teggi, A.; Siracusano, A. Molecular and immunological characterization of the C-terminal region of a new Echinococcus granulosus Heat Shock Protein 70. Parasite Immunol., 2003, 25(3), 119-126.
[http://dx.doi.org/10.1046/j.1365-3024.2003.00617.x] [PMID: 12911519]
[121]
Margutti, P.; Ortona, E.; Vaccari, S.; Barca, S.; Riganò, R.; Teggi, A.; Muhschlegel, F.; Frosch, M.; Siracusano, A. Cloning and expression of a cDNA encoding an elongation factor 1beta/delta protein from Echinococcus granulosus with immunogenic activity. Parasite Immunol., 1999, 21(9), 485-492.
[http://dx.doi.org/10.1046/j.1365-3024.1999.00246.x] [PMID: 10476057]
[122]
Ortona, E.; Margutti, P.; Vaccari, S.; Riganò, R.; Profumo, E.; Buttari, B.; Chersi, A.; Teggi, A.; Siracusano, A. Elongation factor 1 beta/delta of Echinococcus granulosus and allergic manifestations in human cystic echinococcosis. Clin. Exp. Immunol., 2001, 125(1), 110-116.
[http://dx.doi.org/10.1046/j.1365-2249.2001.01569.x] [PMID: 11472433]
[123]
Ortona, E.; Vaccari, S.; Margutti, P.; Delunardo, F.; Rigano, R.; Profumo, E.; Buttari, B.; Rasool, O.; Teggi, A.; Siracusano, A. Immunological characterization of Echinococcus granulosus cyclophilin, an allergen reactive with IgE and IgG4 from patients with cystic echinococcosis. Clin. Exp. Immunol., 2002, 128(1), 124-130.
[http://dx.doi.org/10.1046/j.1365-2249.2002.01807.x] [PMID: 11982600]
[124]
Argaet, V.P.; Mitchell, G.F. Cyclophilin of Schistosoma japonicum. J. Parasitol., 1992, 78(4), 660-664.
[http://dx.doi.org/10.2307/3283541] [PMID: 1635025]
[125]
Shepherd, J.C.; Aitken, A.; McManus, D.P. A protein secreted in vivo by Echinococcus granulosus inhibits elastase activity and neutrophil chemotaxis. Mol. Biochem. Parasitol., 1991, 44(1), 81-90.
[http://dx.doi.org/10.1016/0166-6851(91)90223-S] [PMID: 2011156]
[126]
Riganò, R.; Profumo, E.; Bruschi, F.; Carulli, G.; Azzarà, A.; Ioppolo, S.; Buttari, B.; Ortona, E.; Margutti, P.; Teggi, A.; Siracusano, A. Modulation of human immune response by Echinococcus granulosus antigen B and its possible role in evading host defenses. Infect. Immun., 2001, 69(1), 288-296.
[http://dx.doi.org/10.1128/IAI.69.1.288-296.2001] [PMID: 11119517]
[127]
Sbihi, Y.; Rmiqui, A.; Rodriguez-Cabezas, M.N.; Orduña, A.; Rodriguez-Torres, A.; Osuna, A. Comparative sensitivity of six serological tests and diagnostic value of ELISA using purified antigen in hydatidosis. J. Clin. Lab. Anal., 2001, 15(1), 14-18.
[http://dx.doi.org/10.1002/1098-2825(2001)15:1<14:AID-JCLA3>3.0.CO;2-7] [PMID: 11170228]
[128]
Zhang, L.H.; McManus, D.P. Purification and N-terminal amino acid sequencing of Echinococcus granulosus antigen 5. Parasite Immunol., 1996, 18(12), 597-606.
[http://dx.doi.org/10.1046/j.1365-3024.1996.d01-42.x] [PMID: 9226698]
[129]
Willis, A.C.; Díaz, A.; Nieto, A.; Sim, R.B. Echinococcus granulosus antigen 5 may be a serine proteinase. Parasite Immunol., 1997, 19(8), 385.
[http://dx.doi.org/10.1046/j.1365-3024.1997.d01-222.x] [PMID: 9340598]
[130]
Valmonte, G.R.; Cauyan, G.A.; Ramos, J.D. IgE cross-reactivity between house dust mite allergens and Ascaris lumbricoides antigens. Asia Pac. Allergy, 2012, 2(1), 35-44.
[http://dx.doi.org/10.5415/apallergy.2012.2.1.35] [PMID: 22348205]
[131]
Acevedo, N.; Mohr, J.; Zakzuk, J.; Samonig, M.; Briza, P.; Erler, A.; Pomés, A.; Huber, C.G.; Ferreira, F.; Caraballo, L. Proteomic and immunochemical characterization of glutathione transferase as a new allergen of the nematode Ascaris lumbricoides. PLoS One, 2013, 8(11)e78353
[http://dx.doi.org/10.1371/journal.pone.0078353] [PMID: 24223794]
[132]
Arruda, L.K.; Santos, A.B. Immunologic responses to common antigens in helminthic infections and allergic disease. Curr. Opin. Allergy Clin. Immunol., 2005, 5(5), 399-402.
[http://dx.doi.org/10.1097/01.all.0000182536.55650.d0] [PMID: 16131913]
[133]
Sereda, M.J.; Hartmann, S.; Lucius, R. Helminths and allergy: the example of tropomyosin. Trends Parasitol., 2008, 24(6), 272-278.
[http://dx.doi.org/10.1016/j.pt.2008.03.006] [PMID: 18450511]
[134]
Yong, T.S.; Kim, D.S.; Lee, S.Y.; Im, K.I.; Lee, K.Y. Detection of specific serum IgE in clonorchiasis cases and analysis of Clonorchis sinensis allergens. Yonsei Med. J., 1993, 34(3), 248-257.
[http://dx.doi.org/10.3349/ymj.1993.34.3.248] [PMID: 8259702]
[135]
Santiago, H.C.; Bennuru, S.; Boyd, A.; Eberhard, M.; Nutman, T.B. Structural and immunologic cross-reactivity among filarial and mite tropomyosin: implications for the hygiene hypothesis. J. Allergy Clin. Immunol., 2011, 127(2), 479-486.
[http://dx.doi.org/10.1016/j.jaci.2010.11.007] [PMID: 21185070]
[136]
Bernardini, R.; Mistrello, G.; Novembre, E.; Roncarolo, D.; Zanotta, S.; Lombardi, E.; Cianferoni, A.; Pucci, N.; De Martino, M.; Vierucci, A. Cross-reactivity between IgE-binding proteins from Anisakis simplex and Dermatophagoides pteronyssinus. Int. J. Immunopathol. Pharmacol., 2005, 18(4), 671-675.
[http://dx.doi.org/10.1177/039463200501800408] [PMID: 16388714]
[137]
Santos, A.B.; Rocha, G.M.; Oliver, C.; Ferriani, V.P.; Lima, R.C.; Palma, M.S.; Sales, V.S.; Aalberse, R.C.; Chapman, M.D.; Arruda, L.K. Cross-reactive IgE antibody responses to tropomyosins from Ascaris lumbricoides and cockroach. J. Allergy Clin. Immunol., 2008, 121(4), 1040-6.e1.
[http://dx.doi.org/10.1016/j.jaci.2007.12.1147] [PMID: 18275995]
[138]
Acevedo, N.; Erler, A.; Briza, P.; Puccio, F.; Ferreira, F.; Caraballo, L. Allergenicity of Ascaris lumbricoides tropomyosin and IgE sensitization among asthmatic patients in a tropical environment. Int. Arch. Allergy Immunol., 2011, 154(3), 195-206.
[http://dx.doi.org/10.1159/000321106] [PMID: 20861641]
[139]
Asnoussi, A.; Aibinu, I.E.; Gasser, R.B.; Lopata, A.L.; Smooker, P.M. Molecular and immunological characterisation of tropomyosin from Anisakis pegreffii. Parasitol. Res., 2017, 116(12), 3291-3301.
[http://dx.doi.org/10.1007/s00436-017-5642-4] [PMID: 29038898]
[140]
Jenkins, R.E.; Taylor, M.J.; Gilvary, N.J.; Bianco, A.E. Tropomyosin implicated in host protective responses to microfilariae in onchocerciasis. Proc. Natl. Acad. Sci. USA, 1998, 95(13), 7550-7555.
[http://dx.doi.org/10.1073/pnas.95.13.7550] [PMID: 9636187]
[141]
Santiago, H.C. LeeVan, E.; Bennuru, S.; Ribeiro-Gomes, F.; Mueller, E.; Wilson, M.; Wynn, T.; Garboczi, D.; Urban, J.; Mitre, E.; Nutman, T.B. Molecular mimicry between cockroach and helminth glutathione S-transferases promotes cross-reactivity and cross-sensitization. J. Allergy Clin. Immunol., 2012, 130(1), 248-56.e9.
[http://dx.doi.org/10.1016/j.jaci.2012.02.045] [PMID: 22541242]
[142]
Mueller, G.A.; Pedersen, L.C.; Glesner, J.; Edwards, L.L.; Zakzuk, J.; London, R.E.; Arruda, L.K.; Chapman, M.D.; Caraballo, L.; Pomés, A. Analysis of glutathione S-transferase allergen cross-reactivity in a North American population: Relevance for molecular diagnosis. J. Allergy Clin. Immunol., 2015, 136(5), 1369-1377.
[http://dx.doi.org/10.1016/j.jaci.2015.03.015] [PMID: 25930195]
[143]
Rodríguez-Pérez, R.; Monsalve, R.I.; Galán, A.; Perez-Piñar, T.; Umpierrez, A.; Lluch-Bernal, M.; Polo, F.; Caballero, M.L. Cross-reactivity between Anisakis spp. and wasp venom allergens. Int. Arch. Allergy Immunol., 2014, 163(3), 179-184.
[http://dx.doi.org/10.1159/000358060] [PMID: 24525615]
[144]
Chandrashekar, R.; Curtis, K.C.; Weil, G.J. Molecular characterization of a parasite antigen in sera from onchocerciasis patients that is immunologically cross-reactive with human keratin. J. Infect. Dis., 1995, 171(6), 1586-1592.
[http://dx.doi.org/10.1093/infdis/171.6.1586] [PMID: 7539474]
[145]
Moneo, I.; Carballeda-Sangiao, N.; González-Muñoz, M. New Perspectives on the Diagnosis of Allergy to Anisakis spp. Curr. Allergy Asthma Rep., 2017, 17(5), 27.
[http://dx.doi.org/10.1007/s11882-017-0698-x] [PMID: 28429304]
[146]
Johansson, E.; Aponno, M.; Lundberg, M.; van Hage-Hamsten, M. Allergenic cross-reactivity between the nematode Anisakis simplex and the dust mites Acarus siro, Lepidoglyphus destructor, Tyrophagus putrescentiae, and Dermatophagoides pteronyssinus. Allergy, 2001, 56(7), 660-666.
[http://dx.doi.org/10.1034/j.1398-9995.2001.00798.x] [PMID: 11421925]
[147]
Heffler, E.; Sberna, M.E.; Sichili, S.; Intravaia, R.; Nicolosi, G.; Porto, M.; Liuzzo, M.T.; Picardi, G.; Fichera, S.; Crimi, N. High prevalence of Anisakis simplex hypersensitivity and allergy in Sicily, Italy. Ann. Allergy Asthma Immunol., 2016, 116(2), 146-150.
[http://dx.doi.org/10.1016/j.anai.2015.12.014] [PMID: 26815707]
[148]
Baeza, M.L.; Rodríguez, A.; Matheu, V.; Rubio, M.; Tornero, P.; de Barrio, M.; Herrero, T.; Santaolalla, M.; Zubeldia, J.M. Characterization of allergens secreted by Anisakis simplex parasite: clinical relevance in comparison with somatic allergens. Clin. Exp. Allergy, 2004, 34(2), 296-302.
[http://dx.doi.org/10.1111/j.1365-2222.2004.01883.x] [PMID: 14987311]
[149]
Chung, Y.B.; Lee, J. Clinical characteristics of gastroallergic anisakiasis and diagnostic implications of immunologic tests. Allergy Asthma Immunol. Res., 2014, 6(3), 228-233.
[http://dx.doi.org/10.4168/aair.2014.6.3.228] [PMID: 24843798]
[150]
Gutiérrez, R.; Cuéllar, C. Immunoglobulins anti-Anisakis simplex in patients with gastrointestinal diseases. J. Helminthol., 2002, 76(2), 131-136.
[http://dx.doi.org/10.1079/JOH2001104] [PMID: 12015825]
[151]
Andreu-Ballester, J.C.; Pérez-Griera, J.; Ballester, F.; Colomer-Rubio, E.; Ortiz-Tarín, I.; Pelayo, V.; Rodero, M.; Cuéllar, C. Anisakis simplex and Kudoa sp.: evaluation of specific antibodies in appendectomized patients. Exp. Parasitol., 2008, 119(3), 433-436.
[http://dx.doi.org/10.1016/j.exppara.2008.03.014] [PMID: 18456263]
[152]
Caraballo, L.; Coronado, S. Parasite allergens. Mol. Immunol., 2018, 100, 113-119.
[http://dx.doi.org/10.1016/j.molimm.2018.03.014] [PMID: 29588070]
[153]
Ahumada, V.; García, E.; Dennis, R.; Rojas, M.X.; Rondón, M.A.; Pérez, A.; Peñaranda, A.; Barragán, A.M.; Jimenez, S.; Kennedy, M.W.; Caraballo, L. IgE responses to Ascaris and mite tropomyosins are risk factors for asthma. Clin. Exp. Allergy, 2015, 45(7), 1189-1200.
[http://dx.doi.org/10.1111/cea.12513] [PMID: 25702830]
[154]
Hawdon, J.M.; Hotez, P.J. Hookworm: developmental biology of the infectious process. Curr. Opin. Genet. Dev., 1996, 6(5), 618-623.
[http://dx.doi.org/10.1016/S0959-437X(96)80092-X] [PMID: 8939719]
[155]
Osman, A.; Wang, C.K.; Winter, A.; Loukas, A.; Tribolet, L.; Gasser, R.B.; Hofmann, A. Hookworm SCP/TAPS protein structure--A key to understanding host-parasite interactions and developing new interventions. Biotechnol. Adv., 2012, 30(3), 652-657.
[http://dx.doi.org/10.1016/j.biotechadv.2011.11.002] [PMID: 22120067]
[156]
Bethony, J.; Loukas, A.; Smout, M.; Brooker, S.; Mendez, S.; Plieskatt, J.; Goud, G.; Bottazzi, M.E.; Zhan, B.; Wang, Y.; Williamson, A.; Lustigman, S.; Correa-Oliveira, R.; Xiao, S.; Hotez, P.J. Antibodies against a secreted protein from hookworm larvae reduce the intensity of hookworm infection in humans and vaccinated laboratory animals. FASEB J., 2005, 19(12), 1743-1745.
[http://dx.doi.org/10.1096/fj.05-3936fje] [PMID: 16037096]
[157]
Radauer, C.; Bublin, M.; Wagner, S.; Mari, A.; Breiteneder, H. Allergens are distributed into few protein families and possess a restricted number of biochemical functions. J. Allergy Clin. Immunol., 2008, 121(4), 847-52.e7.
[http://dx.doi.org/10.1016/j.jaci.2008.01.025] [PMID: 18395549]
[158]
Dunne, D.W.; Butterworth, A.E.; Fulford, A.J.; Kariuki, H.C.; Langley, J.G.; Ouma, J.H.; Capron, A.; Pierce, R.J.; Sturrock, R.F. Immunity after treatment of human schistosomiasis: association between IgE antibodies to adult worm antigens and resistance to reinfection. Eur. J. Immunol., 1992, 22(6), 1483-1494.
[http://dx.doi.org/10.1002/eji.1830220622] [PMID: 1601036]
[159]
Dunne, D.W.; Webster, M.; Smith, P.; Langley, J.G.; Richardson, B.A.; Fulford, A.J.; Butterworth, A.E.; Sturrock, R.F.; Kariuki, H.C.; Ouma, J.H. The isolation of a 22 kDa band after SDS-PAGE of Schistosoma mansoni adult worms and its use to demonstrate that IgE responses against the antigen(s) it contains are associated with human resistance to reinfection. Parasite Immunol., 1997, 19(2), 79-89.
[http://dx.doi.org/10.1046/j.1365-3024.1997.d01-186.x] [PMID: 9076810]
[160]
Jiz, M.; Friedman, J.F.; Leenstra, T.; Jarilla, B.; Pablo, A.; Langdon, G.; Pond-Tor, S.; Wu, H.W.; Manalo, D.; Olveda, R.; Acosta, L.; Kurtis, J.D.; Immunoglobulin, E.; Immunoglobulin, E. IgE) responses to paramyosin predict resistance to reinfection with Schistosoma japonicum and are attenuated by IgG4. Infect. Immun., 2009, 77(5), 2051-2058.
[http://dx.doi.org/10.1128/IAI.00012-09] [PMID: 19273558]
[161]
Stein, L.D.; David, J.R. Cloning of a developmentally regulated tegument antigen of Schistosoma mansoni. Mol. Biochem. Parasitol., 1986, 20(3), 253-264.
[http://dx.doi.org/10.1016/0166-6851(86)90106-4] [PMID: 2429181]
[162]
Pinot de Moira, A.; Fulford, A.J.; Kabatereine, N.B.; Ouma, J.H.; Booth, M.; Dunne, D.W. Analysis of complex patterns of human exposure and immunity to Schistosomiasis mansoni: the influence of age, sex, ethnicity and IgE. PLoS Negl. Trop. Dis., 2010, 4(9)e820
[http://dx.doi.org/10.1371/journal.pntd.0000820] [PMID: 20856909]
[163]
Webster, M.; Fulford, A.J.; Braun, G.; Ouma, J.H.; Kariuki, H.C.; Havercroft, J.C.; Gachuhi, K.; Sturrock, R.F.; Butterworth, A.E.; Dunne, D.W. Human immunoglobulin E responses to a recombinant 22.6-kilodalton antigen from Schistosoma mansoni adult worms are associated with low intensities of reinfection after treatment. Infect. Immun., 1996, 64(10), 4042-4046.
[PMID: 8926066]
[164]
Wan, D.; Ludolf, F.; Alanine, D.G.; Stretton, O.; Ali Ali, E.; Al-Barwary, N.; Wang, X.; Doenhoff, M.J.; Mari, A.; Fitzsimmons, C.M.; Dunne, D.W.; Nakamura, R.; Oliveira, G.C.; Alcocer, M.J.; Falcone, F.H. Use of humanised rat basophilic leukaemia cell line RS-ATL8 for the assessment of allergenicity of Schistosoma mansoni proteins. PLoS Negl. Trop. Dis., 2014, 8(9)e3124
[http://dx.doi.org/10.1371/journal.pntd.0003124] [PMID: 25254513]
[165]
Fitzsimmons, C.M.; Jones, F.M.; Stearn, A.; Chalmers, I.W.; Hoffmann, K.F.; Wawrzyniak, J.; Wilson, S.; Kabatereine, N.B.; Dunne, D.W. The Schistosoma mansoni tegumental-allergen-like (TAL) protein family: influence of developmental expression on human IgE responses. PLoS Negl. Trop. Dis., 2012, 6(4) e1593
[http://dx.doi.org/10.1371/journal.pntd.0001593] [PMID: 22509417]
[166]
Fitzsimmons, C.M.; Jones, F.M.; Pinot de Moira, A.; Protasio, A.V.; Khalife, J.; Dickinson, H.A.; Tukahebwa, E.M.; Dunne, D.W. Progressive cross-reactivity in IgE responses: an explanation for the slow development of human immunity to schistosomiasis? Infect. Immun., 2012, 80(12), 4264-4270.
[http://dx.doi.org/10.1128/IAI.00641-12] [PMID: 23006852]
[167]
Kennedy, M.W. The nematode polyprotein allergens/antigens. Parasitol. Today (Regul. Ed.),, 2000, 16(9), 373-380.
[http://dx.doi.org/10.1016/S0169-4758(00)01743-9] [PMID: 10951596]
[168]
McSharry, C.; Xia, Y.; Holland, C.V.; Kennedy, M.W. Natural immunity to Ascaris lumbricoides associated with immunoglobulin E antibody to ABA-1 allergen and inflammation indicators in children. Infect. Immun., 1999, 67(2), 484-489.
[PMID: 9916049]
[169]
Turner, J.D.; Faulkner, H.; Kamgno, J.; Kennedy, M.W.; Behnke, J.; Boussinesq, M.; Bradley, J.E. Allergen-specific IgE and IgG4 are markers of resistance and susceptibility in a human intestinal nematode infection. Microbes Infect., 2005, 7(7-8), 990-996.
[http://dx.doi.org/10.1016/j.micinf.2005.03.036] [PMID: 15961339]
[170]
Kennedy, M.W.; Brass, A.; McCruden, A.B.; Price, N.C.; Kelly, S.M.; Cooper, A. The ABA-1 allergen of the parasitic nematode Ascaris suum: fatty acid and retinoid binding function and structural characterization. Biochemistry, 1995, 34(20), 6700-6710.
[http://dx.doi.org/10.1021/bi00020a015] [PMID: 7756301]
[171]
Meenan, N.A.; Ball, G.; Bromek, K.; Uhrín, D.; Cooper, A.; Kennedy, M.W.; Smith, B.O. Solution structure of a repeated unit of the ABA-1 nematode polyprotein allergen of Ascaris reveals a novel fold and two discrete lipid-binding sites. PLoS Negl. Trop. Dis., 2011, 5(4)e1040
[http://dx.doi.org/10.1371/journal.pntd.0001040] [PMID: 21526216]
[172]
Rodríguez, E.; Romarís, F.; Lorenzo, S.; Moreno, J.; Bonay, P.; Ubeira, F.M.; Gárate, T. A recombinant enolase from Anisakis simplex is differentially recognized in natural human and mouse experimental infections. Med. Microbiol. Immunol. (Berl.), 2006, 195(1), 1-10.
[http://dx.doi.org/10.1007/s00430-005-0236-7] [PMID: 16049725]
[173]
Quiazon, K.M.; Zenke, K.; Yoshinaga, T. Molecular characterization and comparison of four Anisakis allergens between Anisakis simplex sensu stricto and Anisakis pegreffii from Japan. Mol. Biochem. Parasitol., 2013, 190(1), 23-26.
[http://dx.doi.org/10.1016/j.molbiopara.2013.05.006] [PMID: 23742817]
[174]
Nieuwenhuizen, N.E.; Meter, J.M.; Horsnell, W.G.; Hoving, J.C.; Fick, L.; Sharp, M.F.; Darby, M.G.; Parihar, S.P.; Brombacher, F.; Lopata, A.L. A cross-reactive monoclonal antibody to nematode haemoglobin enhances protective immune responses to Nippostrongylus brasiliensis. PLoS Negl. Trop. Dis., 2013, 297.e2395
[175]
Profumo, E.; Ortona, E.; Riganò, R.; Gioia, I.; Notargiacomo, S.; Ioppolo, S.; Siracusano, A. Cellular and humoral responses to antigenic subunits of Echinococcus granulosus cyst fluid in hydatid patients. Parasite Immunol., 1994, 16(8), 393-398.
[http://dx.doi.org/10.1111/j.1365-3024.1994.tb00366.x] [PMID: 7528907]
[176]
Riganò, R.; Ioppolo, S.; Ortona, E.; Margutti, P.; Profumo, E.; Ali, M.D.; Di Vico, B.; Teggi, A.; Siracusano, A. Long-term serological evaluation of patients with cystic echinococcosis treated with benzimidazole carbamates. Clin. Exp. Immunol., 2002, 129(3), 485-492.
[http://dx.doi.org/10.1046/j.1365-2249.2002.01925.x] [PMID: 12197890]
[177]
Khabiri, A.R.; Bagheri, F.; Assmar, M.; Siavashi, M.R. Analysis of specific IgE and IgG subclass antibodies for diagnosis of Echinococcus granulosus. Parasite Immunol., 2006, 28(8), 357-362.
[http://dx.doi.org/10.1111/j.1365-3024.2006.00837.x] [PMID: 16879307]
[178]
Xia, Y.; Spence, H.J.; Moore, J.; Heaney, N.; McDermott, L.; Cooper, A.; Watson, D.G.; Mei, B.; Komuniecki, R.; Kennedy, M.W. The ABA-1 allergen of Ascaris lumbricoides: sequence polymorphism, stage and tissue-specific expression, lipid binding function, and protein biophysical properties. Parasitology, 2000, 120(Pt 2), 211-224.
[http://dx.doi.org/10.1017/S0031182099005363] [PMID: 10726282]
[179]
Bhattacharyya, T.; Santra, A.; Majumder, D.N.; Chatterjee, B.P. Possible approach for serodiagnosis of ascariasis by evaluation of immunoglobulin G4 response using Ascaris lumbricoides somatic antigen. J. Clin. Microbiol., 2001, 39(8), 2991-2994.
[http://dx.doi.org/10.1128/JCM.39.8.2991-2994.2001] [PMID: 11474031]
[180]
Christie, J.F.; Dunbar, B.; Davidson, I.; Kennedy, M.W. N-terminal amino acid sequence identity between a major allergen of Ascaris lumbricoides and Ascaris suum, and MHC-restricted IgE responses to it. Immunology, 1990, 69(4), 596-602.
[PMID: 2335378]
[181]
Zakzuk, J.; Acevedo, N.; Cifuentes, L.; Bornacelly, A.; Sánchez, J.; Ahumada, V.; Ring, J.; Ollert, M.; Caraballo, L. Early life IgE responses in children living in the tropics: a prospective analysis. Pediatr. Allergy Immunol., 2013, 24(8), 788-797.
[http://dx.doi.org/10.1111/pai.12161] [PMID: 24299508]
[182]
Sereda, M.J.; Hartmann, S.; Büttner, D.W.; Volkmer, R.; Hovestädt, M.; Brattig, N.; Lucius, R. Characterization of the allergen filarial tropomyosin with an invertebrate specific monoclonal antibody. Acta Trop., 2010, 116(1), 61-67.
[http://dx.doi.org/10.1016/j.actatropica.2010.05.010] [PMID: 20525500]
[183]
Webster, M.; Correa-Oliveira, R.; Gazzinelli, G.; Viana, I.R.; Fraga, L.A.; Silveira, A.M.; Dunne, D.W. Factors affecting high and low human IgE responses to schistosome worm antigens in an area of Brazil endemic for Schistosoma mansoni and hookworm. Am. J. Trop. Med. Hyg., 1997, 57(4), 487-494.
[http://dx.doi.org/10.4269/ajtmh.1997.57.487] [PMID: 9347969]
[184]
Fitzsimmons, C.M.; McBeath, R.; Joseph, S.; Jones, F.M.; Walter, K.; Hoffmann, K.F.; Kariuki, H.C.; Mwatha, J.K.; Kimani, G.; Kabatereine, N.B.; Vennervald, B.J.; Ouma, J.H.; Dunne, D.W. Factors affecting human IgE and IgG responses to allergen-like Schistosoma mansoni antigens: Molecular structure and patterns of in vivo exposure. Int. Arch. Allergy Immunol., 2007, 142(1), 40-50.
[http://dx.doi.org/10.1159/000095997] [PMID: 17019080]
[185]
de Oliveira Fraga, L.A.; Lamb, E.W.; Moreno, E.C.; Chatterjee, M.; Dvořák, J.; Delcroix, M.; Sajid, M.; Caffrey, C.R.; Davies, S.J. Rapid induction of IgE responses to a worm cysteine protease during murine pre-patent schistosome infection. BMC Immunol., 2010, 11, 56.
[http://dx.doi.org/10.1186/1471-2172-11-56] [PMID: 21078176]
[186]
Shankar, J.; Gupta, P.D.; Sridhara, S.; Singh, B.P.; Gaur, S.N.; Arora, N. Immunobiochemical analysis of cross-reactive glutathione-S-transferase allergen from different fungal sources. Immunol. Invest., 2005, 34(1), 37-51.
[http://dx.doi.org/10.1081/IMM-47383] [PMID: 15773571]
[187]
Jiz, M.; Wu, H.W.; Meng, R.; Pond-Tor, S.; Reynolds, M.; Friedman, J.F.; Olveda, R.; Acosta, L.; Kurtis, J.D. Pilot-scale production and characterization of paramyosin, a vaccine candidate for schistosomiasis japonica. Infect. Immun., 2008, 76(7), 3164-3169.
[http://dx.doi.org/10.1128/IAI.00409-08] [PMID: 18426875]
[188]
Santiago, M.L.; Hafalla, J.C.; Kurtis, J.D.; Aligui, G.L.; Wiest, P.M.; Olveda, R.M.; Olds, G.R.; Dunne, D.W.; Ramirez, B.L. Identification of the Schistosoma japonicum 22.6-kDa antigen as a major target of the human IgE response: similarity of IgE-binding epitopes to allergen peptides. Int. Arch. Allergy Immunol., 1998, 117(2), 94-104.
[http://dx.doi.org/10.1159/000023995] [PMID: 9784652]
[189]
Kurtis, J.D.; Ramirez, B.L.; Wiest, P.M.; Dong, K.L.; El-Meanawy, A.; Petzke, M.M.; Johnson, J.H.; Edmison, J.; Maier, R.A., Jr; Olds, G.R. Identification and molecular cloning of a 67-kilodalton protein in Schistosoma japonicum homologous to a family of actin-binding proteins. Infect. Immun., 1997, 65(1), 344-347.
[PMID: 8975937]
[190]
Rathaur, S.; Fischer, P.; Domagalski, M.; Walter, R.D.; Liebau, E. Brugia malayi and Wuchereria bancrofti: gene comparison and recombinant expression of pi-class related glutathione S-transferases. Exp. Parasitol., 2003, 103(3-4), 177-181.
[http://dx.doi.org/10.1016/S0014-4894(03)00093-6] [PMID: 12880597]
[191]
Krushna, N.S.A.; Shiny, C.; Dharanya, S.; Sindhu, A.; Aishwarya, S.; Narayanan, R.B. Immunolocalization and serum antibody responses to Brugia malayi pepsin inhibitor homolog (Bm-33). Microbiol. Immunol., 2009, 53(3), 173-183.
[http://dx.doi.org/10.1111/j.1348-0421.2009.00114.x] [PMID: 19302528]
[192]
Salinas, G.; Braun, G.; Taylor, D.W. Molecular characterisation and localisation of an Onchocerca volvulus pi-class glutathione S-transferase. Mol. Biochem. Parasitol., 1994, 66(1), 1-9.
[http://dx.doi.org/10.1016/0166-6851(94)90030-2] [PMID: 7984170]
[193]
Lucius, R.; Kern, A.; Seeber, F.; Pogonka, T.; Willenbücher, J.; Taylor, H.R.; Pinder, M.; Ghalib, H.W.; Schulz-Key, H.; Soboslay, P. Specific and sensitive IgG4 immunodiagnosis of onchocerciasis with a recombinant 33 kD Onchocerca volvulus protein (Ov33). Trop. Med. Parasitol., 1992, 43(3), 139-145.
[PMID: 1281926]
[194]
Zhan, B.; Santiago, H.; Keegan, B.; Gillespie, P.; Xue, J.; Bethony, J.; de Oliveira, L.M.; Jiang, D.; Diemert, D.; Xiao, S.H.; Jones, K.; Feng, X.; Hotez, P.J.; Bottazzi, M.E. Fusion of Na-ASP-2 with human immunoglobulin Fcγ abrogates histamine release from basophils sensitized with anti-Na-ASP-2 IgE. Parasite Immunol., 2012, 34(8-9), 404-411.
[http://dx.doi.org/10.1111/j.1365-3024.2012.01371.x] [PMID: 22651670]
[195]
Pritchard, D.I.; Brown, A.; Kasper, G.; McElroy, P.; Loukas, A.; Hewitt, C.; Berry, C.; Füllkrug, R.; Beck, E. A hookworm allergen which strongly resembles calreticulin. Parasite Immunol., 1999, 21(9), 439-450.
[http://dx.doi.org/10.1046/j.1365-3024.1999.00238.x] [PMID: 10476053]
[196]
Mohamad, S.; Azmi, N.C.; Noordin, R. Development and evaluation of a sensitive and specific assay for diagnosis of human toxocariasis by use of three recombinant antigens (TES-26, TES-30USM, and TES-120). J. Clin. Microbiol., 2009, 47(6), 1712-1717.
[http://dx.doi.org/10.1128/JCM.00001-09] [PMID: 19369434]
[197]
Zocevic, A.; Mace, P.; Vallee, I.; Blaga, R.; Liu, M.; Lacour, S.A.; Boireau, P. Identification of Trichinella spiralis early antigens at the pre-adult and adult stages. Parasitology, 2011, 138(4), 463-471.
[http://dx.doi.org/10.1017/S0031182010001526] [PMID: 21092349]
[198]
Nakada, T.; Nagano, I.; Wu, Z.; Takahashi, Y. Molecular cloning and expression of the full-length tropomyosin gene from Trichinella spiralis. J. Helminthol., 2003, 77(1), 57-63.
[http://dx.doi.org/10.1079/JOH2002153] [PMID: 12590666]
[199]
Varatharajalu, R.; Parandaman, V.; Ndao, M.; Andersen, J.F.; Neva, F.A. Strongyloides stercoralis excretory/secretory protein strongylastacin specifically recognized by IgE antibodies in infected human sera. Microbiol. Immunol., 2011, 55(2), 115-122.
[http://dx.doi.org/10.1111/j.1348-0421.2010.00289.x] [PMID: 21204942]
[200]
Ramachandran, S.; Thompson, R.W.; Gam, A.A.; Neva, F.A. Recombinant cDNA clones for immunodiagnosis of strongyloidiasis. J. Infect. Dis., 1998, 177(1), 196-203.
[http://dx.doi.org/10.1086/513817] [PMID: 9419188]
[201]
Ravi, V.; Ramachandran, S.; Thompson, R.W.; Andersen, J.F.; Neva, F.A. Characterization of a recombinant immunodiagnostic antigen (NIE) from Strongyloides stercoralis L3-stage larvae. Mol. Biochem. Parasitol., 2002, 125(1-2), 73-81.
[http://dx.doi.org/10.1016/S0166-6851(02)00214-1] [PMID: 12467975]
[202]
Reese, G.; Ayuso, R.; Lehrer, S.B. Tropomyosin: an invertebrate pan-allergen. Int. Arch. Allergy Immunol., 1999, 119(4), 247-258.
[http://dx.doi.org/10.1159/000024201] [PMID: 10474029]
[203]
Nara, T.; Tanabe, K.; Mahakunkijcharoen, Y.; Osada, Y.; Matsumoto, N.; Kita, K.; Kojima, S. The B cell epitope of paramyosin recognized by a protective monoclonal IgE antibody to Schistosoma japonicum. Vaccine, 1997, 15(1), 79-84.
[http://dx.doi.org/10.1016/S0264-410X(96)00100-4] [PMID: 9041670]

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