Genetic immunisation by liver stage antigen 3 protects chimpanzees against malaria despite low immune responses.

BACKGROUND: The true interest of genetic immunisation might have been hastily underestimated based on overall immunogenicity data in humans and lack of parallelism with other, more classical immunisation methods. PRINCIPAL FINDINGS: Using malaria Liver Stage Antigen-3 (LSA-3), we report that genetic...

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Main Authors: Pierre Daubersies, Benjamin Ollomo, Jean-Pierre Sauzet, Karima Brahimi, Blanca-Liliana Perlaza, Wijnand Eling, Hubert Moukana, Pierre Rouquet, Charles de Taisne, Pierre Druilhe
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2008-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2441826?pdf=render
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spelling doaj-e7faa32e289c45b3ae692c98247555412020-11-25T02:22:09ZengPublic Library of Science (PLoS)PLoS ONE1932-62032008-01-0137e265910.1371/journal.pone.0002659Genetic immunisation by liver stage antigen 3 protects chimpanzees against malaria despite low immune responses.Pierre DaubersiesBenjamin OllomoJean-Pierre SauzetKarima BrahimiBlanca-Liliana PerlazaWijnand ElingHubert MoukanaPierre RouquetCharles de TaisnePierre DruilheBACKGROUND: The true interest of genetic immunisation might have been hastily underestimated based on overall immunogenicity data in humans and lack of parallelism with other, more classical immunisation methods. PRINCIPAL FINDINGS: Using malaria Liver Stage Antigen-3 (LSA-3), we report that genetic immunization induces in chimpanzees, the closest relative of humans, immune responses which are as scarce as those reported using other DNA vaccines in humans, but which nonetheless confer strong, sterile and reproducible protection. The pattern was consistent in 3/4 immunized apes against two high dose sporozoite challenges performed as late as 98 and 238 days post-immunization and by a heterologous strain. CONCLUSIONS: These results should, in our opinion, lead to a revisiting of the value of this unusual means of immunisation, using as a model a disease, malaria, in which virulent challenges of volunteers are ethically acceptable.http://europepmc.org/articles/PMC2441826?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Pierre Daubersies
Benjamin Ollomo
Jean-Pierre Sauzet
Karima Brahimi
Blanca-Liliana Perlaza
Wijnand Eling
Hubert Moukana
Pierre Rouquet
Charles de Taisne
Pierre Druilhe
spellingShingle Pierre Daubersies
Benjamin Ollomo
Jean-Pierre Sauzet
Karima Brahimi
Blanca-Liliana Perlaza
Wijnand Eling
Hubert Moukana
Pierre Rouquet
Charles de Taisne
Pierre Druilhe
Genetic immunisation by liver stage antigen 3 protects chimpanzees against malaria despite low immune responses.
PLoS ONE
author_facet Pierre Daubersies
Benjamin Ollomo
Jean-Pierre Sauzet
Karima Brahimi
Blanca-Liliana Perlaza
Wijnand Eling
Hubert Moukana
Pierre Rouquet
Charles de Taisne
Pierre Druilhe
author_sort Pierre Daubersies
title Genetic immunisation by liver stage antigen 3 protects chimpanzees against malaria despite low immune responses.
title_short Genetic immunisation by liver stage antigen 3 protects chimpanzees against malaria despite low immune responses.
title_full Genetic immunisation by liver stage antigen 3 protects chimpanzees against malaria despite low immune responses.
title_fullStr Genetic immunisation by liver stage antigen 3 protects chimpanzees against malaria despite low immune responses.
title_full_unstemmed Genetic immunisation by liver stage antigen 3 protects chimpanzees against malaria despite low immune responses.
title_sort genetic immunisation by liver stage antigen 3 protects chimpanzees against malaria despite low immune responses.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2008-01-01
description BACKGROUND: The true interest of genetic immunisation might have been hastily underestimated based on overall immunogenicity data in humans and lack of parallelism with other, more classical immunisation methods. PRINCIPAL FINDINGS: Using malaria Liver Stage Antigen-3 (LSA-3), we report that genetic immunization induces in chimpanzees, the closest relative of humans, immune responses which are as scarce as those reported using other DNA vaccines in humans, but which nonetheless confer strong, sterile and reproducible protection. The pattern was consistent in 3/4 immunized apes against two high dose sporozoite challenges performed as late as 98 and 238 days post-immunization and by a heterologous strain. CONCLUSIONS: These results should, in our opinion, lead to a revisiting of the value of this unusual means of immunisation, using as a model a disease, malaria, in which virulent challenges of volunteers are ethically acceptable.
url http://europepmc.org/articles/PMC2441826?pdf=render
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