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Schistosoma mansoni schistosomula antigens induce Th1/Pro‐inflammatory cytokine responses

Larvae of Schistosoma (schistosomula) are highly susceptible to host immune responses and are attractive prophylactic vaccine targets, although cellular immune responses against schistosomula antigens in endemic human populations are not well characterized. We collected blood and stool from 54 Schis...

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Autores principales: Egesa, Moses, Lubyayi, Lawrence, Tukahebwa, Edridah M., Bagaya, Bernard S., Chalmers, Iain W., Wilson, Shona, Hokke, Cornelis H., Hoffmann, Karl F., Dunne, David W., Yazdanbakhsh, Maria, Labuda, Lucja A., Cose, Stephen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6492251/
https://www.ncbi.nlm.nih.gov/pubmed/30239006
http://dx.doi.org/10.1111/pim.12592
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author Egesa, Moses
Lubyayi, Lawrence
Tukahebwa, Edridah M.
Bagaya, Bernard S.
Chalmers, Iain W.
Wilson, Shona
Hokke, Cornelis H.
Hoffmann, Karl F.
Dunne, David W.
Yazdanbakhsh, Maria
Labuda, Lucja A.
Cose, Stephen
author_facet Egesa, Moses
Lubyayi, Lawrence
Tukahebwa, Edridah M.
Bagaya, Bernard S.
Chalmers, Iain W.
Wilson, Shona
Hokke, Cornelis H.
Hoffmann, Karl F.
Dunne, David W.
Yazdanbakhsh, Maria
Labuda, Lucja A.
Cose, Stephen
author_sort Egesa, Moses
collection PubMed
description Larvae of Schistosoma (schistosomula) are highly susceptible to host immune responses and are attractive prophylactic vaccine targets, although cellular immune responses against schistosomula antigens in endemic human populations are not well characterized. We collected blood and stool from 54 Schistosoma mansoni‐infected Ugandans, isolated peripheral blood mononuclear cells and stimulated them for 24 hours with schistosome adult worm and soluble egg antigens (AWA and SEA), along with schistosomula recombinant proteins rSmKK7, Lymphocyte Antigen 6 isoforms (rSmLy6A and rSmLy6B), tetraspanin isoforms (rSmTSP6 and rSmTSP7). Cytokines, chemokines and growth factors were measured in the culture supernatants using a multiplex luminex assay, and infection intensity was determined before and at 1 year after praziquantel (PZQ) treatment using the Kato‐Katz method. Cellular responses were grouped and the relationship between groups of correlated cellular responses and infection intensity before and after PZQ treatment was investigated. AWA and SEA induced mainly Th2 responses. In contrast, rSmLy6B, rSmTSP6 and rSmTSP7 induced Th1/pro‐inflammatory responses. While recombinant antigens rSmKK7 and rSmLy6A did not induce a Th1/pro‐inflammatory response, they had an association with pre‐treatment infection intensity after adjusting for age and sex. Testing more schistosomula antigens using this approach could provide immune‐epidemiology identifiers necessary for prioritizing next generation schistosomiasis vaccine candidates.
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spelling pubmed-64922512019-05-07 Schistosoma mansoni schistosomula antigens induce Th1/Pro‐inflammatory cytokine responses Egesa, Moses Lubyayi, Lawrence Tukahebwa, Edridah M. Bagaya, Bernard S. Chalmers, Iain W. Wilson, Shona Hokke, Cornelis H. Hoffmann, Karl F. Dunne, David W. Yazdanbakhsh, Maria Labuda, Lucja A. Cose, Stephen Parasite Immunol Original Articles Larvae of Schistosoma (schistosomula) are highly susceptible to host immune responses and are attractive prophylactic vaccine targets, although cellular immune responses against schistosomula antigens in endemic human populations are not well characterized. We collected blood and stool from 54 Schistosoma mansoni‐infected Ugandans, isolated peripheral blood mononuclear cells and stimulated them for 24 hours with schistosome adult worm and soluble egg antigens (AWA and SEA), along with schistosomula recombinant proteins rSmKK7, Lymphocyte Antigen 6 isoforms (rSmLy6A and rSmLy6B), tetraspanin isoforms (rSmTSP6 and rSmTSP7). Cytokines, chemokines and growth factors were measured in the culture supernatants using a multiplex luminex assay, and infection intensity was determined before and at 1 year after praziquantel (PZQ) treatment using the Kato‐Katz method. Cellular responses were grouped and the relationship between groups of correlated cellular responses and infection intensity before and after PZQ treatment was investigated. AWA and SEA induced mainly Th2 responses. In contrast, rSmLy6B, rSmTSP6 and rSmTSP7 induced Th1/pro‐inflammatory responses. While recombinant antigens rSmKK7 and rSmLy6A did not induce a Th1/pro‐inflammatory response, they had an association with pre‐treatment infection intensity after adjusting for age and sex. Testing more schistosomula antigens using this approach could provide immune‐epidemiology identifiers necessary for prioritizing next generation schistosomiasis vaccine candidates. John Wiley and Sons Inc. 2018-10-21 2018-12 /pmc/articles/PMC6492251/ /pubmed/30239006 http://dx.doi.org/10.1111/pim.12592 Text en © 2018 The Authors. Parasite Immunology Published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Egesa, Moses
Lubyayi, Lawrence
Tukahebwa, Edridah M.
Bagaya, Bernard S.
Chalmers, Iain W.
Wilson, Shona
Hokke, Cornelis H.
Hoffmann, Karl F.
Dunne, David W.
Yazdanbakhsh, Maria
Labuda, Lucja A.
Cose, Stephen
Schistosoma mansoni schistosomula antigens induce Th1/Pro‐inflammatory cytokine responses
title Schistosoma mansoni schistosomula antigens induce Th1/Pro‐inflammatory cytokine responses
title_full Schistosoma mansoni schistosomula antigens induce Th1/Pro‐inflammatory cytokine responses
title_fullStr Schistosoma mansoni schistosomula antigens induce Th1/Pro‐inflammatory cytokine responses
title_full_unstemmed Schistosoma mansoni schistosomula antigens induce Th1/Pro‐inflammatory cytokine responses
title_short Schistosoma mansoni schistosomula antigens induce Th1/Pro‐inflammatory cytokine responses
title_sort schistosoma mansoni schistosomula antigens induce th1/pro‐inflammatory cytokine responses
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6492251/
https://www.ncbi.nlm.nih.gov/pubmed/30239006
http://dx.doi.org/10.1111/pim.12592
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