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Peptide-pulsed dendritic cells induce antigen-specific CTL-mediated protective tumor immunity

Cytotoxic T lymphocytes (CTLs) are a critical component of the immune response to tumors. Tumor-derived peptide antigens targeted by CTLs are being defined for several human tumors and are potential immunogens for the induction of specific antitumor immunity. Dendritic cells (DC) are potent antigen-...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1996
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2192396/
https://www.ncbi.nlm.nih.gov/pubmed/8551233
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collection PubMed
description Cytotoxic T lymphocytes (CTLs) are a critical component of the immune response to tumors. Tumor-derived peptide antigens targeted by CTLs are being defined for several human tumors and are potential immunogens for the induction of specific antitumor immunity. Dendritic cells (DC) are potent antigen-presenting cells (APCs) capable of priming CTL responses in vivo. Here we show that major histocompatibility complex class I- presented peptide antigen pulsed onto dendritic APCs induces protective immunity to lethal challenge by a tumor transfected with the antigen gene. The immunity is antigen specific, requiring expression of the antigen gene by the tumor target, and is eliminated by in vivo depletion of CD8+ T cells. Furthermore, mice that have rejected the transfected tumor are protected from subsequent challenge with the untransfected parent tumor. These results suggest that immunization strategies using antigen-pulsed DC may be useful for inducing tumor- specific immune responses.
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spelling pubmed-21923962008-04-16 Peptide-pulsed dendritic cells induce antigen-specific CTL-mediated protective tumor immunity J Exp Med Articles Cytotoxic T lymphocytes (CTLs) are a critical component of the immune response to tumors. Tumor-derived peptide antigens targeted by CTLs are being defined for several human tumors and are potential immunogens for the induction of specific antitumor immunity. Dendritic cells (DC) are potent antigen-presenting cells (APCs) capable of priming CTL responses in vivo. Here we show that major histocompatibility complex class I- presented peptide antigen pulsed onto dendritic APCs induces protective immunity to lethal challenge by a tumor transfected with the antigen gene. The immunity is antigen specific, requiring expression of the antigen gene by the tumor target, and is eliminated by in vivo depletion of CD8+ T cells. Furthermore, mice that have rejected the transfected tumor are protected from subsequent challenge with the untransfected parent tumor. These results suggest that immunization strategies using antigen-pulsed DC may be useful for inducing tumor- specific immune responses. The Rockefeller University Press 1996-01-01 /pmc/articles/PMC2192396/ /pubmed/8551233 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Peptide-pulsed dendritic cells induce antigen-specific CTL-mediated protective tumor immunity
title Peptide-pulsed dendritic cells induce antigen-specific CTL-mediated protective tumor immunity
title_full Peptide-pulsed dendritic cells induce antigen-specific CTL-mediated protective tumor immunity
title_fullStr Peptide-pulsed dendritic cells induce antigen-specific CTL-mediated protective tumor immunity
title_full_unstemmed Peptide-pulsed dendritic cells induce antigen-specific CTL-mediated protective tumor immunity
title_short Peptide-pulsed dendritic cells induce antigen-specific CTL-mediated protective tumor immunity
title_sort peptide-pulsed dendritic cells induce antigen-specific ctl-mediated protective tumor immunity
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2192396/
https://www.ncbi.nlm.nih.gov/pubmed/8551233