"Negative vaccination" by specific CD4 T cell tolerisation enhances virus-specific protective antibody responses.
BACKGROUND: Cooperation of CD4+ T helper cells with specific B cells is crucial for protective vaccination against pathogens by inducing long-lived neutralizing antibody responses. During infection with persistence-prone viruses, prolonged virus replication correlates with low neutralizing antibody...
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doaj-524c80c646cf44d89bd069f2d6e6fb462020-11-25T02:38:51ZengPublic Library of Science (PLoS)PLoS ONE1932-62032007-01-01211e116210.1371/journal.pone.0001162"Negative vaccination" by specific CD4 T cell tolerisation enhances virus-specific protective antibody responses.Karl S LangAhmed N HegazyPhilipp A LangBruno EschliMax LöhningHans HengartnerRolf M ZinkernagelMike RecherBACKGROUND: Cooperation of CD4+ T helper cells with specific B cells is crucial for protective vaccination against pathogens by inducing long-lived neutralizing antibody responses. During infection with persistence-prone viruses, prolonged virus replication correlates with low neutralizing antibody responses. We recently described that a viral mutant of lymphocytic choriomeningitis virus (LCMV), which lacks a T helper epitope, counterintuitively induced an enhanced protective antibody response. Likewise, partial depletion of the CD4+ T cell compartment by using anti-CD4 antibodies enhanced protective antibodies. PRINCIPAL FINDINGS: Here we have developed a protocol to selectively reduce the CD4+ T cell response against viral CD4+ T cell epitopes. We demonstrate that in vivo treatment with LCMV-derived MHC-II peptides induced non-responsiveness of specific CD4+ T cells without affecting CD4+ T cell reactivity towards other antigens. This was associated with accelerated virus-specific neutralizing IgG-antibody responses. In contrast to a complete absence of CD4+ T cell help, tolerisation did not impair CD8+ T cell responses. CONCLUSIONS: This result reveals a novel "negative vaccination" strategy where specific CD4+ T cell unresponsiveness may be used to enhance the delayed protective antibody responses in chronic virus infections.http://europepmc.org/articles/PMC2048666?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Karl S Lang Ahmed N Hegazy Philipp A Lang Bruno Eschli Max Löhning Hans Hengartner Rolf M Zinkernagel Mike Recher |
spellingShingle |
Karl S Lang Ahmed N Hegazy Philipp A Lang Bruno Eschli Max Löhning Hans Hengartner Rolf M Zinkernagel Mike Recher "Negative vaccination" by specific CD4 T cell tolerisation enhances virus-specific protective antibody responses. PLoS ONE |
author_facet |
Karl S Lang Ahmed N Hegazy Philipp A Lang Bruno Eschli Max Löhning Hans Hengartner Rolf M Zinkernagel Mike Recher |
author_sort |
Karl S Lang |
title |
"Negative vaccination" by specific CD4 T cell tolerisation enhances virus-specific protective antibody responses. |
title_short |
"Negative vaccination" by specific CD4 T cell tolerisation enhances virus-specific protective antibody responses. |
title_full |
"Negative vaccination" by specific CD4 T cell tolerisation enhances virus-specific protective antibody responses. |
title_fullStr |
"Negative vaccination" by specific CD4 T cell tolerisation enhances virus-specific protective antibody responses. |
title_full_unstemmed |
"Negative vaccination" by specific CD4 T cell tolerisation enhances virus-specific protective antibody responses. |
title_sort |
"negative vaccination" by specific cd4 t cell tolerisation enhances virus-specific protective antibody responses. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2007-01-01 |
description |
BACKGROUND: Cooperation of CD4+ T helper cells with specific B cells is crucial for protective vaccination against pathogens by inducing long-lived neutralizing antibody responses. During infection with persistence-prone viruses, prolonged virus replication correlates with low neutralizing antibody responses. We recently described that a viral mutant of lymphocytic choriomeningitis virus (LCMV), which lacks a T helper epitope, counterintuitively induced an enhanced protective antibody response. Likewise, partial depletion of the CD4+ T cell compartment by using anti-CD4 antibodies enhanced protective antibodies. PRINCIPAL FINDINGS: Here we have developed a protocol to selectively reduce the CD4+ T cell response against viral CD4+ T cell epitopes. We demonstrate that in vivo treatment with LCMV-derived MHC-II peptides induced non-responsiveness of specific CD4+ T cells without affecting CD4+ T cell reactivity towards other antigens. This was associated with accelerated virus-specific neutralizing IgG-antibody responses. In contrast to a complete absence of CD4+ T cell help, tolerisation did not impair CD8+ T cell responses. CONCLUSIONS: This result reveals a novel "negative vaccination" strategy where specific CD4+ T cell unresponsiveness may be used to enhance the delayed protective antibody responses in chronic virus infections. |
url |
http://europepmc.org/articles/PMC2048666?pdf=render |
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