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Schistosoma mansoni infection induces plasmablast and plasma cell death in the bone marrow and accelerates the decline of host vaccine responses
Schistosomiasis is a potentially lethal parasitic disease that profoundly impacts systemic immune function in chronically infected hosts through mechanisms that remain unknown. Given the immunoregulatory dysregulation experienced in infected individuals, this study examined the impact of chronic sch...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8893680/ https://www.ncbi.nlm.nih.gov/pubmed/35157732 http://dx.doi.org/10.1371/journal.ppat.1010327 |
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author | Musaigwa, Fungai Kamdem, Severin Donald Mpotje, Thabo Mosala, Paballo Abdel Aziz, Nada Herbert, De’Broski R. Brombacher, Frank Nono, Justin Komguep |
author_facet | Musaigwa, Fungai Kamdem, Severin Donald Mpotje, Thabo Mosala, Paballo Abdel Aziz, Nada Herbert, De’Broski R. Brombacher, Frank Nono, Justin Komguep |
author_sort | Musaigwa, Fungai |
collection | PubMed |
description | Schistosomiasis is a potentially lethal parasitic disease that profoundly impacts systemic immune function in chronically infected hosts through mechanisms that remain unknown. Given the immunoregulatory dysregulation experienced in infected individuals, this study examined the impact of chronic schistosomiasis on the sustainability of vaccine-induced immunity in both children living in endemic areas and experimental infections in mice. Data show that chronic Schistosoma mansoni infection impaired the persistence of vaccine specific antibody responses in poliovirus-vaccinated humans and mice. Mechanistically, schistosomiasis primarily fostered plasmablast and plasma cell death in the bone marrow and removal of parasites following praziquantel treatment reversed the observed cell death and partially restored vaccine-induced memory responses associated with increased serum anti-polio antibody responses. Our findings strongly suggest a previously unrecognized mechanism to explain how chronic schistosomiasis interferes with an otherwise effective vaccine regimen and further advocates for therapeutic intervention strategies that reduce schistosomiasis burden in endemic areas prior to vaccination. |
format | Online Article Text |
id | pubmed-8893680 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-88936802022-03-04 Schistosoma mansoni infection induces plasmablast and plasma cell death in the bone marrow and accelerates the decline of host vaccine responses Musaigwa, Fungai Kamdem, Severin Donald Mpotje, Thabo Mosala, Paballo Abdel Aziz, Nada Herbert, De’Broski R. Brombacher, Frank Nono, Justin Komguep PLoS Pathog Research Article Schistosomiasis is a potentially lethal parasitic disease that profoundly impacts systemic immune function in chronically infected hosts through mechanisms that remain unknown. Given the immunoregulatory dysregulation experienced in infected individuals, this study examined the impact of chronic schistosomiasis on the sustainability of vaccine-induced immunity in both children living in endemic areas and experimental infections in mice. Data show that chronic Schistosoma mansoni infection impaired the persistence of vaccine specific antibody responses in poliovirus-vaccinated humans and mice. Mechanistically, schistosomiasis primarily fostered plasmablast and plasma cell death in the bone marrow and removal of parasites following praziquantel treatment reversed the observed cell death and partially restored vaccine-induced memory responses associated with increased serum anti-polio antibody responses. Our findings strongly suggest a previously unrecognized mechanism to explain how chronic schistosomiasis interferes with an otherwise effective vaccine regimen and further advocates for therapeutic intervention strategies that reduce schistosomiasis burden in endemic areas prior to vaccination. Public Library of Science 2022-02-14 /pmc/articles/PMC8893680/ /pubmed/35157732 http://dx.doi.org/10.1371/journal.ppat.1010327 Text en © 2022 Musaigwa et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Musaigwa, Fungai Kamdem, Severin Donald Mpotje, Thabo Mosala, Paballo Abdel Aziz, Nada Herbert, De’Broski R. Brombacher, Frank Nono, Justin Komguep Schistosoma mansoni infection induces plasmablast and plasma cell death in the bone marrow and accelerates the decline of host vaccine responses |
title | Schistosoma mansoni infection induces plasmablast and plasma cell death in the bone marrow and accelerates the decline of host vaccine responses |
title_full | Schistosoma mansoni infection induces plasmablast and plasma cell death in the bone marrow and accelerates the decline of host vaccine responses |
title_fullStr | Schistosoma mansoni infection induces plasmablast and plasma cell death in the bone marrow and accelerates the decline of host vaccine responses |
title_full_unstemmed | Schistosoma mansoni infection induces plasmablast and plasma cell death in the bone marrow and accelerates the decline of host vaccine responses |
title_short | Schistosoma mansoni infection induces plasmablast and plasma cell death in the bone marrow and accelerates the decline of host vaccine responses |
title_sort | schistosoma mansoni infection induces plasmablast and plasma cell death in the bone marrow and accelerates the decline of host vaccine responses |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8893680/ https://www.ncbi.nlm.nih.gov/pubmed/35157732 http://dx.doi.org/10.1371/journal.ppat.1010327 |
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