Cargando…
Risk assessment for the implementation of controlled human Schistosoma mansoni infection trials in Uganda
Schistosomiasis is a parasitic infection highly prevalent in sub-Saharan Africa, and a significant cause of morbidity; it is a priority for vaccine development. A controlled human infection model for Schistosoma mansoni (CHI-S) with potential to accelerate vaccine development has been developed amon...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000 Research Limited
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6901351/ https://www.ncbi.nlm.nih.gov/pubmed/31819922 http://dx.doi.org/10.12688/aasopenres.12972.2 |
_version_ | 1783477481362161664 |
---|---|
author | Koopman, Jan Pieter Egesa, Moses Wajja, Anne Adriko, Moses Nassuuna, Jacent Nkurunungi, Gyaviira Driciru, Emmanuella van Willigen, Gijsbert Cose, Stephen Yazdanbakhsh, Maria Kaleebu, Pontiano Kabatereine, Narcis Tukahebwa, Edridah Roestenberg, Meta Elliott, Alison M. |
author_facet | Koopman, Jan Pieter Egesa, Moses Wajja, Anne Adriko, Moses Nassuuna, Jacent Nkurunungi, Gyaviira Driciru, Emmanuella van Willigen, Gijsbert Cose, Stephen Yazdanbakhsh, Maria Kaleebu, Pontiano Kabatereine, Narcis Tukahebwa, Edridah Roestenberg, Meta Elliott, Alison M. |
author_sort | Koopman, Jan Pieter |
collection | PubMed |
description | Schistosomiasis is a parasitic infection highly prevalent in sub-Saharan Africa, and a significant cause of morbidity; it is a priority for vaccine development. A controlled human infection model for Schistosoma mansoni (CHI-S) with potential to accelerate vaccine development has been developed among naïve volunteers in the Netherlands. Because responses both to infections and candidate vaccines are likely to differ between endemic and non-endemic settings, we propose to establish a CHI-S in Uganda where Schistosoma mansoni is endemic. As part of a “road-map” to this goal, we have undertaken a risk assessment. We identified risks related to importing of laboratory vector snails and schistosome strains from the Netherlands to Uganda; exposure to natural infection in endemic settings concurrently with CHI-S studies, and unfamiliarity of the community with the nature, risks and rationale for CHI. Mitigating strategies are proposed. With careful implementation of the latter, we believe that CHI-S can be implemented safely in Uganda. Our reflections are presented here to promote feedback and discussion. |
format | Online Article Text |
id | pubmed-6901351 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | F1000 Research Limited |
record_format | MEDLINE/PubMed |
spelling | pubmed-69013512019-12-09 Risk assessment for the implementation of controlled human Schistosoma mansoni infection trials in Uganda Koopman, Jan Pieter Egesa, Moses Wajja, Anne Adriko, Moses Nassuuna, Jacent Nkurunungi, Gyaviira Driciru, Emmanuella van Willigen, Gijsbert Cose, Stephen Yazdanbakhsh, Maria Kaleebu, Pontiano Kabatereine, Narcis Tukahebwa, Edridah Roestenberg, Meta Elliott, Alison M. AAS Open Res Open Letter Schistosomiasis is a parasitic infection highly prevalent in sub-Saharan Africa, and a significant cause of morbidity; it is a priority for vaccine development. A controlled human infection model for Schistosoma mansoni (CHI-S) with potential to accelerate vaccine development has been developed among naïve volunteers in the Netherlands. Because responses both to infections and candidate vaccines are likely to differ between endemic and non-endemic settings, we propose to establish a CHI-S in Uganda where Schistosoma mansoni is endemic. As part of a “road-map” to this goal, we have undertaken a risk assessment. We identified risks related to importing of laboratory vector snails and schistosome strains from the Netherlands to Uganda; exposure to natural infection in endemic settings concurrently with CHI-S studies, and unfamiliarity of the community with the nature, risks and rationale for CHI. Mitigating strategies are proposed. With careful implementation of the latter, we believe that CHI-S can be implemented safely in Uganda. Our reflections are presented here to promote feedback and discussion. F1000 Research Limited 2019-08-13 /pmc/articles/PMC6901351/ /pubmed/31819922 http://dx.doi.org/10.12688/aasopenres.12972.2 Text en Copyright: © 2019 Koopman JP et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Open Letter Koopman, Jan Pieter Egesa, Moses Wajja, Anne Adriko, Moses Nassuuna, Jacent Nkurunungi, Gyaviira Driciru, Emmanuella van Willigen, Gijsbert Cose, Stephen Yazdanbakhsh, Maria Kaleebu, Pontiano Kabatereine, Narcis Tukahebwa, Edridah Roestenberg, Meta Elliott, Alison M. Risk assessment for the implementation of controlled human Schistosoma mansoni infection trials in Uganda |
title | Risk assessment for the implementation of controlled human
Schistosoma mansoni infection trials in Uganda |
title_full | Risk assessment for the implementation of controlled human
Schistosoma mansoni infection trials in Uganda |
title_fullStr | Risk assessment for the implementation of controlled human
Schistosoma mansoni infection trials in Uganda |
title_full_unstemmed | Risk assessment for the implementation of controlled human
Schistosoma mansoni infection trials in Uganda |
title_short | Risk assessment for the implementation of controlled human
Schistosoma mansoni infection trials in Uganda |
title_sort | risk assessment for the implementation of controlled human
schistosoma mansoni infection trials in uganda |
topic | Open Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6901351/ https://www.ncbi.nlm.nih.gov/pubmed/31819922 http://dx.doi.org/10.12688/aasopenres.12972.2 |
work_keys_str_mv | AT koopmanjanpieter riskassessmentfortheimplementationofcontrolledhumanschistosomamansoniinfectiontrialsinuganda AT egesamoses riskassessmentfortheimplementationofcontrolledhumanschistosomamansoniinfectiontrialsinuganda AT wajjaanne riskassessmentfortheimplementationofcontrolledhumanschistosomamansoniinfectiontrialsinuganda AT adrikomoses riskassessmentfortheimplementationofcontrolledhumanschistosomamansoniinfectiontrialsinuganda AT nassuunajacent riskassessmentfortheimplementationofcontrolledhumanschistosomamansoniinfectiontrialsinuganda AT nkurunungigyaviira riskassessmentfortheimplementationofcontrolledhumanschistosomamansoniinfectiontrialsinuganda AT driciruemmanuella riskassessmentfortheimplementationofcontrolledhumanschistosomamansoniinfectiontrialsinuganda AT vanwilligengijsbert riskassessmentfortheimplementationofcontrolledhumanschistosomamansoniinfectiontrialsinuganda AT cosestephen riskassessmentfortheimplementationofcontrolledhumanschistosomamansoniinfectiontrialsinuganda AT yazdanbakhshmaria riskassessmentfortheimplementationofcontrolledhumanschistosomamansoniinfectiontrialsinuganda AT kaleebupontiano riskassessmentfortheimplementationofcontrolledhumanschistosomamansoniinfectiontrialsinuganda AT kabatereinenarcis riskassessmentfortheimplementationofcontrolledhumanschistosomamansoniinfectiontrialsinuganda AT tukahebwaedridah riskassessmentfortheimplementationofcontrolledhumanschistosomamansoniinfectiontrialsinuganda AT roestenbergmeta riskassessmentfortheimplementationofcontrolledhumanschistosomamansoniinfectiontrialsinuganda AT elliottalisonm riskassessmentfortheimplementationofcontrolledhumanschistosomamansoniinfectiontrialsinuganda |