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Identification of a CD4+ T cell-stimulating antigen of pathogenic bacteria by expression cloning

Identifying the immunogenic proteins that elicit pathogen-specific T cell responses is key to rational vaccine design. While several approaches have succeeded in identifying major histocompatibility complex (MHC) class I bound peptides that stimulate CD8+ T cells, these approaches have been difficul...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1995
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2192246/
https://www.ncbi.nlm.nih.gov/pubmed/7500019
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collection PubMed
description Identifying the immunogenic proteins that elicit pathogen-specific T cell responses is key to rational vaccine design. While several approaches have succeeded in identifying major histocompatibility complex (MHC) class I bound peptides that stimulate CD8+ T cells, these approaches have been difficult to extend to peptides presented by MHC class II molecules that stimulate CD4+ T cells. We describe here a novel strategy for identifying CD4+ T cell-stimulating antigen genes. Using Listeria monocytogenes-specific, lacZ-inducible T cells as single- cell probes, we screened a Listeria monocytogenes genomic library as recombinant Escherichia coli that were fed to macrophages. The antigen gene was isolated from the E. coli clone that, when ingested by the macrophages, allowed generation of the appropriate peptide/MHC class II complex and T cell activation. We show that the antigenic peptide is derived from a previously unknown listeria gene product with characteristics of a membrane-bound protein.
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spelling pubmed-21922462008-04-16 Identification of a CD4+ T cell-stimulating antigen of pathogenic bacteria by expression cloning J Exp Med Articles Identifying the immunogenic proteins that elicit pathogen-specific T cell responses is key to rational vaccine design. While several approaches have succeeded in identifying major histocompatibility complex (MHC) class I bound peptides that stimulate CD8+ T cells, these approaches have been difficult to extend to peptides presented by MHC class II molecules that stimulate CD4+ T cells. We describe here a novel strategy for identifying CD4+ T cell-stimulating antigen genes. Using Listeria monocytogenes-specific, lacZ-inducible T cells as single- cell probes, we screened a Listeria monocytogenes genomic library as recombinant Escherichia coli that were fed to macrophages. The antigen gene was isolated from the E. coli clone that, when ingested by the macrophages, allowed generation of the appropriate peptide/MHC class II complex and T cell activation. We show that the antigenic peptide is derived from a previously unknown listeria gene product with characteristics of a membrane-bound protein. The Rockefeller University Press 1995-12-01 /pmc/articles/PMC2192246/ /pubmed/7500019 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
Identification of a CD4+ T cell-stimulating antigen of pathogenic bacteria by expression cloning
title Identification of a CD4+ T cell-stimulating antigen of pathogenic bacteria by expression cloning
title_full Identification of a CD4+ T cell-stimulating antigen of pathogenic bacteria by expression cloning
title_fullStr Identification of a CD4+ T cell-stimulating antigen of pathogenic bacteria by expression cloning
title_full_unstemmed Identification of a CD4+ T cell-stimulating antigen of pathogenic bacteria by expression cloning
title_short Identification of a CD4+ T cell-stimulating antigen of pathogenic bacteria by expression cloning
title_sort identification of a cd4+ t cell-stimulating antigen of pathogenic bacteria by expression cloning
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2192246/
https://www.ncbi.nlm.nih.gov/pubmed/7500019