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Impact of malaria and helminth infections on immunogenicity of the human papillomavirus-16/18 AS04-adjuvanted vaccine in Tanzania()()

BACKGROUND: 

 Endemic malaria and helminth infections in sub-Saharan Africa can act as immunological modulators and impact responses to standard immunizations. We conducted a cohort study to measure the influence of malaria and helminth infections on the immunogenicity of the bivalent HPV-16/18 vac...

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Autores principales: Brown, Joelle, Baisley, Kathy, Kavishe, Bazil, Changalucha, John, Andreasen, Aura, Mayaud, Philippe, Gumodoka, Balthazar, Kapiga, Saidi, Hayes, Richard, Watson-Jones, Deborah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3898269/
https://www.ncbi.nlm.nih.gov/pubmed/24291193
http://dx.doi.org/10.1016/j.vaccine.2013.11.061
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author Brown, Joelle
Baisley, Kathy
Kavishe, Bazil
Changalucha, John
Andreasen, Aura
Mayaud, Philippe
Gumodoka, Balthazar
Kapiga, Saidi
Hayes, Richard
Watson-Jones, Deborah
author_facet Brown, Joelle
Baisley, Kathy
Kavishe, Bazil
Changalucha, John
Andreasen, Aura
Mayaud, Philippe
Gumodoka, Balthazar
Kapiga, Saidi
Hayes, Richard
Watson-Jones, Deborah
author_sort Brown, Joelle
collection PubMed
description BACKGROUND: 

 Endemic malaria and helminth infections in sub-Saharan Africa can act as immunological modulators and impact responses to standard immunizations. We conducted a cohort study to measure the influence of malaria and helminth infections on the immunogenicity of the bivalent HPV-16/18 vaccine. METHODS: 

 We evaluated the association between malaria and helminth infections, and HPV-16/18 antibody responses among 298 Tanzanian females aged 10–25 years enrolled in a randomized controlled trial of the HPV-16/18 vaccine. Malaria parasitaemia was diagnosed by examination of blood smears, and helminth infections were diagnosed by examination of urine and stool samples, respectively. Geometric mean antibody titres (GMT) against HPV-16/18 antibodies were measured by enzyme-linked immunosorbent assay. RESULTS: 

 Parasitic infections were common; one-third (30.4%) of participants had a helminth infection and 10.2% had malaria parasitaemia. Overall, the vaccine induced high HPV-16/18 GMTs, and there was no evidence of a reduction in HPV-16 or HPV-18 GMT at Month 7 or Month 12 follow-up visits among participants with helminths or malaria. There was some evidence that participants with malaria had increased GMTs compared to those without malaria. CONCLUSIONS: 

 The data show high HPV immunogenicity regardless of the presence of malaria and helminth infections. The mechanism and significance for the increase in GMT in those with malaria is unknown.
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spelling pubmed-38982692014-01-24 Impact of malaria and helminth infections on immunogenicity of the human papillomavirus-16/18 AS04-adjuvanted vaccine in Tanzania()() Brown, Joelle Baisley, Kathy Kavishe, Bazil Changalucha, John Andreasen, Aura Mayaud, Philippe Gumodoka, Balthazar Kapiga, Saidi Hayes, Richard Watson-Jones, Deborah Vaccine Article BACKGROUND: 

 Endemic malaria and helminth infections in sub-Saharan Africa can act as immunological modulators and impact responses to standard immunizations. We conducted a cohort study to measure the influence of malaria and helminth infections on the immunogenicity of the bivalent HPV-16/18 vaccine. METHODS: 

 We evaluated the association between malaria and helminth infections, and HPV-16/18 antibody responses among 298 Tanzanian females aged 10–25 years enrolled in a randomized controlled trial of the HPV-16/18 vaccine. Malaria parasitaemia was diagnosed by examination of blood smears, and helminth infections were diagnosed by examination of urine and stool samples, respectively. Geometric mean antibody titres (GMT) against HPV-16/18 antibodies were measured by enzyme-linked immunosorbent assay. RESULTS: 

 Parasitic infections were common; one-third (30.4%) of participants had a helminth infection and 10.2% had malaria parasitaemia. Overall, the vaccine induced high HPV-16/18 GMTs, and there was no evidence of a reduction in HPV-16 or HPV-18 GMT at Month 7 or Month 12 follow-up visits among participants with helminths or malaria. There was some evidence that participants with malaria had increased GMTs compared to those without malaria. CONCLUSIONS: 

 The data show high HPV immunogenicity regardless of the presence of malaria and helminth infections. The mechanism and significance for the increase in GMT in those with malaria is unknown. Elsevier Science 2014-01-23 /pmc/articles/PMC3898269/ /pubmed/24291193 http://dx.doi.org/10.1016/j.vaccine.2013.11.061 Text en © 2013 The Authors https://creativecommons.org/licenses/by/3.0/This is an open access article under the CC BY license (https://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Brown, Joelle
Baisley, Kathy
Kavishe, Bazil
Changalucha, John
Andreasen, Aura
Mayaud, Philippe
Gumodoka, Balthazar
Kapiga, Saidi
Hayes, Richard
Watson-Jones, Deborah
Impact of malaria and helminth infections on immunogenicity of the human papillomavirus-16/18 AS04-adjuvanted vaccine in Tanzania()()
title Impact of malaria and helminth infections on immunogenicity of the human papillomavirus-16/18 AS04-adjuvanted vaccine in Tanzania()()
title_full Impact of malaria and helminth infections on immunogenicity of the human papillomavirus-16/18 AS04-adjuvanted vaccine in Tanzania()()
title_fullStr Impact of malaria and helminth infections on immunogenicity of the human papillomavirus-16/18 AS04-adjuvanted vaccine in Tanzania()()
title_full_unstemmed Impact of malaria and helminth infections on immunogenicity of the human papillomavirus-16/18 AS04-adjuvanted vaccine in Tanzania()()
title_short Impact of malaria and helminth infections on immunogenicity of the human papillomavirus-16/18 AS04-adjuvanted vaccine in Tanzania()()
title_sort impact of malaria and helminth infections on immunogenicity of the human papillomavirus-16/18 as04-adjuvanted vaccine in tanzania()()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3898269/
https://www.ncbi.nlm.nih.gov/pubmed/24291193
http://dx.doi.org/10.1016/j.vaccine.2013.11.061
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