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Effect of four rounds of annual school‐wide mass praziquantel treatment for schistosoma mansoni control on schistosome‐specific immune responses

This study evaluated potential changes in antischistosome immune responses in children from schools that received 4 rounds of annual mass drug administration (MDA) of praziquantel (PZQ). In a repeated cross‐sectional study design, 210 schistosome egg‐positive children were recruited at baseline from...

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Autores principales: Ndombi, E. M., Abudho, B., Kittur, N., Carter, J. M., Korir, H., Riner, D. K., Ochanda, H., Lee, Y‐M., Secor, W. E., Karanja, D. M., Colley, D. G.
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/PMC6001474/
https://www.ncbi.nlm.nih.gov/pubmed/29604074
http://dx.doi.org/10.1111/pim.12530
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author Ndombi, E. M.
Abudho, B.
Kittur, N.
Carter, J. M.
Korir, H.
Riner, D. K.
Ochanda, H.
Lee, Y‐M.
Secor, W. E.
Karanja, D. M.
Colley, D. G.
author_facet Ndombi, E. M.
Abudho, B.
Kittur, N.
Carter, J. M.
Korir, H.
Riner, D. K.
Ochanda, H.
Lee, Y‐M.
Secor, W. E.
Karanja, D. M.
Colley, D. G.
author_sort Ndombi, E. M.
collection PubMed
description This study evaluated potential changes in antischistosome immune responses in children from schools that received 4 rounds of annual mass drug administration (MDA) of praziquantel (PZQ). In a repeated cross‐sectional study design, 210 schistosome egg‐positive children were recruited at baseline from schools in western Kenya (baseline group). Another 251 children of the same age range were recruited from the same schools and diagnosed with schistosome infection by microscopy (post‐MDA group). In‐vitro schistosome‐specific cytokines and plasma antibody levels were measured by ELISA and compared between the 2 groups of children. Schistosome soluble egg antigen (SEA) and soluble worm antigen preparation (SWAP) stimulated higher IL‐5 production by egg‐negative children in the post‐MDA group compared to the baseline group. Similarly, anti‐SEA IgE levels were higher in egg‐negative children in the post‐MDA group compared to the baseline group. Anti‐SEA and anti‐SWAP IgG4 levels were lower in egg‐negative children in the post‐MDA group compared to baseline. This resulted in higher anti‐SEA IgE/IgG4 ratios for children in the post‐MDA group compared to baseline. These post‐MDA immunological changes are compatible with the current paradigm that treatment shifts immune responses to higher antischistosome IgE:IgG4 ratios in parallel with a potential increase in resistance to reinfection.
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spelling pubmed-60014742018-06-21 Effect of four rounds of annual school‐wide mass praziquantel treatment for schistosoma mansoni control on schistosome‐specific immune responses Ndombi, E. M. Abudho, B. Kittur, N. Carter, J. M. Korir, H. Riner, D. K. Ochanda, H. Lee, Y‐M. Secor, W. E. Karanja, D. M. Colley, D. G. Parasite Immunol Original Articles This study evaluated potential changes in antischistosome immune responses in children from schools that received 4 rounds of annual mass drug administration (MDA) of praziquantel (PZQ). In a repeated cross‐sectional study design, 210 schistosome egg‐positive children were recruited at baseline from schools in western Kenya (baseline group). Another 251 children of the same age range were recruited from the same schools and diagnosed with schistosome infection by microscopy (post‐MDA group). In‐vitro schistosome‐specific cytokines and plasma antibody levels were measured by ELISA and compared between the 2 groups of children. Schistosome soluble egg antigen (SEA) and soluble worm antigen preparation (SWAP) stimulated higher IL‐5 production by egg‐negative children in the post‐MDA group compared to the baseline group. Similarly, anti‐SEA IgE levels were higher in egg‐negative children in the post‐MDA group compared to the baseline group. Anti‐SEA and anti‐SWAP IgG4 levels were lower in egg‐negative children in the post‐MDA group compared to baseline. This resulted in higher anti‐SEA IgE/IgG4 ratios for children in the post‐MDA group compared to baseline. These post‐MDA immunological changes are compatible with the current paradigm that treatment shifts immune responses to higher antischistosome IgE:IgG4 ratios in parallel with a potential increase in resistance to reinfection. John Wiley and Sons Inc. 2018-04-29 2018-06 /pmc/articles/PMC6001474/ /pubmed/29604074 http://dx.doi.org/10.1111/pim.12530 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
Ndombi, E. M.
Abudho, B.
Kittur, N.
Carter, J. M.
Korir, H.
Riner, D. K.
Ochanda, H.
Lee, Y‐M.
Secor, W. E.
Karanja, D. M.
Colley, D. G.
Effect of four rounds of annual school‐wide mass praziquantel treatment for schistosoma mansoni control on schistosome‐specific immune responses
title Effect of four rounds of annual school‐wide mass praziquantel treatment for schistosoma mansoni control on schistosome‐specific immune responses
title_full Effect of four rounds of annual school‐wide mass praziquantel treatment for schistosoma mansoni control on schistosome‐specific immune responses
title_fullStr Effect of four rounds of annual school‐wide mass praziquantel treatment for schistosoma mansoni control on schistosome‐specific immune responses
title_full_unstemmed Effect of four rounds of annual school‐wide mass praziquantel treatment for schistosoma mansoni control on schistosome‐specific immune responses
title_short Effect of four rounds of annual school‐wide mass praziquantel treatment for schistosoma mansoni control on schistosome‐specific immune responses
title_sort effect of four rounds of annual school‐wide mass praziquantel treatment for schistosoma mansoni control on schistosome‐specific immune responses
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6001474/
https://www.ncbi.nlm.nih.gov/pubmed/29604074
http://dx.doi.org/10.1111/pim.12530
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