Startseite Anti-Anisakis sp. antibodies in serum of healthy subjects. Relationship with αβ and γδ T cells
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Anti-Anisakis sp. antibodies in serum of healthy subjects. Relationship with αβ and γδ T cells

  • Vega Zamora , Carlos García-Ballesteros , Carmen Benet-Campos , Ferrán Ballester , Carmen Cuéllar EMAIL logo und Juan C. Andreu-Ballester
Veröffentlicht/Copyright: 28. Dezember 2016
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Abstract

Anisakiosis is nowadays one of the nematodoses more prevalent in Spain, with rates that oscillate between 0.43% in Galicia (N.W. Spain), and 15.7% and 22.1% in inland and southern regions, respectively. Likewise, it has been proved that Anisakis larvae have developed mechanisms to modulate the dichotomy of the host immune response for their own benefit. The experimental hypothesis of the present study was that Anisakis sp. larval products can be mediators of immune suppression and induce changes on the populations of αβ+ and γδ+ T cells. In the present study we determined the levels of anti-Anisakis antibodies in the serum of healthy people, and their relationship with the B and T cell subsets. Levels of anti-Anisakis antibodies (Ig’s, IgG, IgM, IgA and IgE) were measured by ELISA, while B and T cell subsets were studied by flow cytometry. Cells were labelled with monoclonal antibodies against CD45, CD4, CD8, CD56, CD3, CD19, TCRαβ and TCRγδ. All the specific isotypes studied were negatively correlated with NKT cell rates with the exception of IgG. A previous contact with Anisakis was related to a decrease in CD56+αβ+ and all γδ+ T cell subsets. The CD3+γδ+ population was lower in the group of subjects that showed IgA anti-Anisakis. We observed an inverse correlation among αβ-γδ NKT cells and anti-Anisakis sp. antibodies. CD3+CD56+ cells showed a significant decrease in the group of anti-Anisakis positive subjects. This fact was especially significant with CD3+CD56+γδ+ cells in the case of the anti-Anisakis IgA positive group.

Acknowledgements

Our thanks go to Dr. AnselmoVillar-Grimalt, Head of Internal Medicine Department, for their unconditional support for our work. This study was partly supported by Fundación Ramón Areces (C.C.).

References

Andreu-Ballester J.C., Tormo-Calandín C., Garcia-Ballesteros C., Amigo V., Peiró-Gómez A., Ruiz del Castillo J., et al. 2014. Increase of IgE anti-Encephalitozoon cuniculi antibodies levels in septic patients. Journal of Clinical and Cellular Immunology, 5, 4. 10.4172/2155-9899.1000244Suche in Google Scholar

Borrelli M., Maglio M., Agnese M., Paparo F., Gentile S., Colicchio B., et al. 2010. High density of intraepithelial gammadelta lymphocytes and deposits of immunoglobulin (Ig)M antitissue transglutaminase antibodies in the jejunum of coeliac patients with IgA deficiency. Clinical and Experimental Immunology, 160, 199–206. 10.1111/j.1365-2249.2009.04077.xSuche in Google Scholar

Brandtzaeg P., Halstensen T.S., Kett K., Krajci P., Kvale D., Rognum T.O., et al. 1989. Immunobiology and immunopathology of human gut mucosa: humoral immunity and intraepithelial lymphocytes. Gastroenterology, 97, 1562–158410.1016/0016-5085(89)90406-XSuche in Google Scholar

Calleja S., Vivas S., Santiuste M., Arias L., Hernando M., Nistal E., et al. 2011. Dynamics of non-conventional intraepithelial lymphocytes-NK, NKT, and γδ T-in celiac disease: relationship with age, diet, and histopathology. Digestive Diseases and Sciences, 56, 2042–2049. 10.1007/s10620-010-1534-5Suche in Google Scholar PubMed

Cuéllar C., Perteguer M.J., de Las Heras, B. 1998. Effects of Anisakis simplex on nitric oxide production in J774 macrophages. Scandinavian Journal of Infectious Diseases, 30, 603–60610.1080/00365549850161179Suche in Google Scholar PubMed

Cuéllar C., Perteguer M.J., Rodero M. 2001. Presence of IL-4-like molecules in larval excretory-secretory products and crude extracts from Anisakis simplex. Scandinavian Journal of Immunology, 53, 483–488. 10.1046/j.1365-3083.2001. 00905.xSuche in Google Scholar

Daschner A., Cuéllar C., Sánchez S., Pascual C., Martín M. 2002. Gastro-allergic anisakiasis as a consequence of simultaneous primary and secondary immune response. Parasite Immunology, 24, 243–251. 10.1046/j.1365-3024.2002.00458.xSuche in Google Scholar PubMed

Fernández de Corres L., del Pozo M.D., Aizpuru F., Buendía E. 2001. Prevalencia de la sensibilización a Anisakis simplex en tresáreas españolas, en relación a las diferentes tasas de consumo de pescado. Relevancia de la alergia a Anisakis simplex. Alergología e Inmunología Clínica, 16, 337–346 (In Spanish)Suche in Google Scholar

Fujii S.I., Shimizu K., Okamoto Y., Kunii N., Nakayama T., Motohashi S., Taniguchi, M. 2013. NKT cells as an ideal anti-tumor immunotherapeutic. Frontiers in Immunology, 4, 409. 10.3389/fimmu.2013.00409Suche in Google Scholar PubMed PubMed Central

Fujimiya Y., Suzuki Y., Katakura R., Miyagi T., Yamaguchi T., Yoshimoto T., Ebina T. 1997. In vitro interleukin 12 activation of peripheral blood CD3(+)CD56(+) and CD3(+)CD56(-) gammadelta T cells from glioblastoma patients. Clinical Cancer Research, 3, 633–643Suche in Google Scholar

García-Hernández P., Rodero M., Cuéllar C. 2007. Anisakis simplex:the activity of larval products on the complement system. Experimental Parasitology, 115, 1–8. 10.1016/j.exppara.2006.04.013Suche in Google Scholar PubMed

García-Hernández P., Rodero M., Cuéllar C. 2009. Study of the effect of Anisakis simplex larval products on the early and late components in the classical complement pathway. Journal of Parasitology, 95, 240–241. 10.1645/ge-1600.1Suche in Google Scholar

García-Palacios L, González M.L., Esteban M.I., Mirabent E., Perteguer M.J., Cuéllar C. 1996. 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. Journal of Helminthology, 70, 281–289. 10.1017/s0022149x0001556xSuche in Google Scholar

Goodman T., Lefrançois L. 1988. Expression of the gamma-delta T-cell receptor on intestinal CD8+ intraepithelial lymphocytes. Nature, 333, 855–858. 10.1038/333855a0Suche in Google Scholar

Green M.R., Kennell A.S., Larche M.J., Seifert M.H., Isenberg D.A., Salaman M.R. 2007. Natural killer T cells in families of patients with systemic lupus erythematosus: their possible role in regulation of IgG production. Arthritis and Rheumathology, 56, 303–310. 10.1002/art.22326Suche in Google Scholar

Gutiérrez R., Cuéllar C. 2002. Immunoglobulins anti-Anisakis simplex in patients with gastrointestinal disease. Journal of Helminthology, 76, 131–136. 10.1079/JOH2001104Suche in Google Scholar

Jones R.E., Deardorff T.L., Kayes S.G. 1990. Anisakis simplex:histopathological changes in experimentally infected CBA/J mice. Experimental Parasitology, 70, 305–313. 10.1016/0014-4894(90)90112-pSuche in Google Scholar

Kabelitz D., Marischen L., Oberg H.H., Holtmeier W., Wesch, D. 2005. Epithelial defence by gamma delta T cells. International Archives of Allergy and Immunology, 37, 73–81. 10.1159/000085107Suche in Google Scholar

Koyama K. 2002. NK1.1+ cell depletion in vivo fails to prevent protection against infection with the murine nematode parasite Trichuris muris. Parasite Immunology, 24, 527–533. 10.1046/j.1365-3024.2002.00497.xSuche in Google Scholar

Mantis N.J., Rol N., Corthésy B. 2011. Secretory IgA’s complex roles in immunity and mucosal homeostasis in the gut. Mucosal Immunology, 4, 603–611. 10.1038/mi.2011.41Suche in Google Scholar

Martínez de Velasco G., Rodero M., Chivato T., Cuéllar C. 2006. Seroprevalence of anti-Kudoa sp. (Myxosporea:Multivalvulida) antibodies in a Spanish population. Parasitology Research, 100, 1205’1211. 10.1007/s00436-006-0390-xSuche in Google Scholar

Morris S.R., Sakanari J.A. 1994. Characterization of the serine protease and serine protease inhibitor from the tissue-penetrating nematode Anisakis simplex. Journal of Biological Chemistry, 269, 27650–2765610.1016/S0021-9258(18)47035-4Suche in Google Scholar

Nutman T.B. 2015. Looking beyond the induction of Th2 responses to explain immunomodulation by helminths. Parasite Immunology, 37, 304–313. 10.1111/pim.12194Suche in Google Scholar

del Rey Moreno A., Valero A., Mayorga C., Gomez B., Torres M.J., Hernandez J., et al. 2006. Sensitization to Anisakis simplex in a healthy population. Acta Tropica, 97, 265–269. 10.1016/j.actatropica.2005.11.007Suche in Google Scholar

Park S.K., Cho M.K., Park H.K., Lee K.H., Lee S.J., Choi S.H., et al.2009. Macrophage migration inhibitory factor homologs of Anisakis simplex suppress Th2 response in allergic airway inflammation model via CD4+CD25+Foxp3+ T cell recruitment. Journal of Immunology, 182, 6907–6914. 10.4049/jimmunol.0803533Suche in Google Scholar

Payne K.K. 2016. Lymphocyte-mediated Immune Regulation in Health and Disease: The Treg and γδ T Cell Co-conspiracy. Immunological Investigations, 12, 1–9. 10.1080/08820139. 2016.1213278Suche in Google Scholar

Perteguer M.J., Raposo R., Cuéllar, C. 1996. In vitro study on the effect of larval excretory/secretory products and crude extracts from Anisakis simplex on blood coagulation. International Journal for Parasitology, 26, 105–108. 10.1016/0020-7519(95)00111-5Suche in Google Scholar

Perteguer M.J., Cuéllar C. 1998. Isotype-specific immune responses in murine experimental anisakiasis. Journal of Veterinary Medicine Series B, 45, 603–610. 10.1111/j.1439-0450.1998.tb00833.xSuche in Google Scholar

Perteguer M.J., Rodero M., Flores J.M., Dórea R.C., Cuéllar C. 2001. Cellular immune responses in mice immunized with Anisakis simplex larval antigens. Parasitology Research, 87, 396–404. 10.1007/s004360000362Suche in Google Scholar

Puente P., Anadón A.M., Rodero M., Romarís F., Ubeira F.M., Cuéllar C. 2008. Anisakis simplex: the high prevalence in Madrid (Spain) and its relation with fish consumption. Experimental Parasitology, 118, 271–274. 10.1016/j.exppara.2007.07.002Suche in Google Scholar

Shen J., Bao S., McClure S.J., Emery D.L., Husband A.J. 2000. Interleukin-6 expression in gut of parasite challenged sheep. Veterinary Immunology and Immunopathology, 76, 163–168. 10.1016/S0165-2427(00)00201-4Suche in Google Scholar

Thaiss C.A., Zmora N., Levy M., Elinav E. 2016. The microbiome and innate immunity. Nature, 535, 65–74. 10.1038/nature18847Suche in Google Scholar PubMed

Valdivieso E., Perteguer M.J., Hurtado C., Campioli P., Rodríguez E., Saborido A., et al. 2015. ANISERP: a new serpin from the parasite Anisakis simplex. Parasites and Vectors, 8, 399. 10.1186/s13071-015-1006-zSuche in Google Scholar PubMed PubMed Central

Valiñas B., Lorenzo S., Eiras A., Figueiras A., Sanmartín M.L., Ubeira F.M. 2001. Prevalence and risk factors for IgE sensitization to Anisakis simplex in a Spanish population. Allergy,56, 667–671. 10.1034/j.1398-9995.2001.00987.xSuche in Google Scholar PubMed

Yoshimoto T., Bendelac A., Watson C., Hu-Li J., Paul W.E. 1995. Role of NK1.1+ T cells in a Th2 response and in IgE production. Science, 270, 1845–1847. 10.1126/science.270.5243.1845Suche in Google Scholar PubMed

Received: 2016-4-9
Revised: 2016-9-21
Accepted: 2016-10-10
Published Online: 2016-12-28
Published in Print: 2017-3-1

© W. Stefański Institute of Parasitology, PAS

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