"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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Main Authors: Karl S Lang, Ahmed N Hegazy, Philipp A Lang, Bruno Eschli, Max Löhning, Hans Hengartner, Rolf M Zinkernagel, Mike Recher
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2007-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2048666?pdf=render
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spelling 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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