Cargando…
The Relationship between RTS,S Vaccine-Induced Antibodies, CD4(+) T Cell Responses and Protection against Plasmodium falciparum Infection
Vaccination with the pre-erythrocytic malaria vaccine RTS,S induces high levels of antibodies and CD4(+) T cells specific for the circumsporozoite protein (CSP). Using a biologically-motivated mathematical model of sporozoite infection fitted to data from malaria-naive adults vaccinated with RTS,S a...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628884/ https://www.ncbi.nlm.nih.gov/pubmed/23613845 http://dx.doi.org/10.1371/journal.pone.0061395 |
_version_ | 1782266479607021568 |
---|---|
author | White, Michael T. Bejon, Philip Olotu, Ally Griffin, Jamie T. Riley, Eleanor M. Kester, Kent E. Ockenhouse, Christian F. Ghani, Azra C. |
author_facet | White, Michael T. Bejon, Philip Olotu, Ally Griffin, Jamie T. Riley, Eleanor M. Kester, Kent E. Ockenhouse, Christian F. Ghani, Azra C. |
author_sort | White, Michael T. |
collection | PubMed |
description | Vaccination with the pre-erythrocytic malaria vaccine RTS,S induces high levels of antibodies and CD4(+) T cells specific for the circumsporozoite protein (CSP). Using a biologically-motivated mathematical model of sporozoite infection fitted to data from malaria-naive adults vaccinated with RTS,S and subjected to experimental P. falciparum challenge, we characterised the relationship between antibodies, CD4(+) T cell responses and protection from infection. Both anti-CSP antibody titres and CSP-specific CD4(+) T cells were identified as immunological surrogates of protection, with RTS,S induced anti-CSP antibodies estimated to prevent 32% (95% confidence interval (CI) 24%–41%) of infections. The addition of RTS,S-induced CSP-specific CD4(+) T cells was estimated to increase vaccine efficacy against infection to 40% (95% CI, 34%–48%). This protective efficacy is estimated to result from a 96.1% (95% CI, 93.4%–97.8%) reduction in the liver-to-blood parasite inoculum, indicating that in volunteers who developed P. falciparum infection, a small number of parasites (often the progeny of a single surviving sporozoite) are responsible for breakthrough blood-stage infections. |
format | Online Article Text |
id | pubmed-3628884 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36288842013-04-23 The Relationship between RTS,S Vaccine-Induced Antibodies, CD4(+) T Cell Responses and Protection against Plasmodium falciparum Infection White, Michael T. Bejon, Philip Olotu, Ally Griffin, Jamie T. Riley, Eleanor M. Kester, Kent E. Ockenhouse, Christian F. Ghani, Azra C. PLoS One Research Article Vaccination with the pre-erythrocytic malaria vaccine RTS,S induces high levels of antibodies and CD4(+) T cells specific for the circumsporozoite protein (CSP). Using a biologically-motivated mathematical model of sporozoite infection fitted to data from malaria-naive adults vaccinated with RTS,S and subjected to experimental P. falciparum challenge, we characterised the relationship between antibodies, CD4(+) T cell responses and protection from infection. Both anti-CSP antibody titres and CSP-specific CD4(+) T cells were identified as immunological surrogates of protection, with RTS,S induced anti-CSP antibodies estimated to prevent 32% (95% confidence interval (CI) 24%–41%) of infections. The addition of RTS,S-induced CSP-specific CD4(+) T cells was estimated to increase vaccine efficacy against infection to 40% (95% CI, 34%–48%). This protective efficacy is estimated to result from a 96.1% (95% CI, 93.4%–97.8%) reduction in the liver-to-blood parasite inoculum, indicating that in volunteers who developed P. falciparum infection, a small number of parasites (often the progeny of a single surviving sporozoite) are responsible for breakthrough blood-stage infections. Public Library of Science 2013-04-16 /pmc/articles/PMC3628884/ /pubmed/23613845 http://dx.doi.org/10.1371/journal.pone.0061395 Text en © 2013 White et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article White, Michael T. Bejon, Philip Olotu, Ally Griffin, Jamie T. Riley, Eleanor M. Kester, Kent E. Ockenhouse, Christian F. Ghani, Azra C. The Relationship between RTS,S Vaccine-Induced Antibodies, CD4(+) T Cell Responses and Protection against Plasmodium falciparum Infection |
title | The Relationship between RTS,S Vaccine-Induced Antibodies, CD4(+) T Cell Responses and Protection against Plasmodium falciparum Infection |
title_full | The Relationship between RTS,S Vaccine-Induced Antibodies, CD4(+) T Cell Responses and Protection against Plasmodium falciparum Infection |
title_fullStr | The Relationship between RTS,S Vaccine-Induced Antibodies, CD4(+) T Cell Responses and Protection against Plasmodium falciparum Infection |
title_full_unstemmed | The Relationship between RTS,S Vaccine-Induced Antibodies, CD4(+) T Cell Responses and Protection against Plasmodium falciparum Infection |
title_short | The Relationship between RTS,S Vaccine-Induced Antibodies, CD4(+) T Cell Responses and Protection against Plasmodium falciparum Infection |
title_sort | relationship between rts,s vaccine-induced antibodies, cd4(+) t cell responses and protection against plasmodium falciparum infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628884/ https://www.ncbi.nlm.nih.gov/pubmed/23613845 http://dx.doi.org/10.1371/journal.pone.0061395 |
work_keys_str_mv | AT whitemichaelt therelationshipbetweenrtssvaccineinducedantibodiescd4tcellresponsesandprotectionagainstplasmodiumfalciparuminfection AT bejonphilip therelationshipbetweenrtssvaccineinducedantibodiescd4tcellresponsesandprotectionagainstplasmodiumfalciparuminfection AT olotually therelationshipbetweenrtssvaccineinducedantibodiescd4tcellresponsesandprotectionagainstplasmodiumfalciparuminfection AT griffinjamiet therelationshipbetweenrtssvaccineinducedantibodiescd4tcellresponsesandprotectionagainstplasmodiumfalciparuminfection AT rileyeleanorm therelationshipbetweenrtssvaccineinducedantibodiescd4tcellresponsesandprotectionagainstplasmodiumfalciparuminfection AT kesterkente therelationshipbetweenrtssvaccineinducedantibodiescd4tcellresponsesandprotectionagainstplasmodiumfalciparuminfection AT ockenhousechristianf therelationshipbetweenrtssvaccineinducedantibodiescd4tcellresponsesandprotectionagainstplasmodiumfalciparuminfection AT ghaniazrac therelationshipbetweenrtssvaccineinducedantibodiescd4tcellresponsesandprotectionagainstplasmodiumfalciparuminfection AT whitemichaelt relationshipbetweenrtssvaccineinducedantibodiescd4tcellresponsesandprotectionagainstplasmodiumfalciparuminfection AT bejonphilip relationshipbetweenrtssvaccineinducedantibodiescd4tcellresponsesandprotectionagainstplasmodiumfalciparuminfection AT olotually relationshipbetweenrtssvaccineinducedantibodiescd4tcellresponsesandprotectionagainstplasmodiumfalciparuminfection AT griffinjamiet relationshipbetweenrtssvaccineinducedantibodiescd4tcellresponsesandprotectionagainstplasmodiumfalciparuminfection AT rileyeleanorm relationshipbetweenrtssvaccineinducedantibodiescd4tcellresponsesandprotectionagainstplasmodiumfalciparuminfection AT kesterkente relationshipbetweenrtssvaccineinducedantibodiescd4tcellresponsesandprotectionagainstplasmodiumfalciparuminfection AT ockenhousechristianf relationshipbetweenrtssvaccineinducedantibodiescd4tcellresponsesandprotectionagainstplasmodiumfalciparuminfection AT ghaniazrac relationshipbetweenrtssvaccineinducedantibodiescd4tcellresponsesandprotectionagainstplasmodiumfalciparuminfection |