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Granulysin-Expressing CD4(+) T Cells as Candidate Immune Marker for Tuberculosis during Childhood and Adolescence

BACKGROUND: Granulysin produced by cytolytic T cells directly contributes to immune defense against tuberculosis (TB). We investigated granulysin as a candidate immune marker for childhood and adolescent TB. METHODS: Peripheral blood mononuclear cells (PBMC) from children and adolescents (1–17 years...

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Autores principales: Mueller, Henrik, Faé, Kellen C., Magdorf, Klaus, Ganoza, Christian A., Wahn, Ulrich, Guhlich, Ute, Feiterna-Sperling, Cornelia, Kaufmann, Stefan H. E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3246496/
https://www.ncbi.nlm.nih.gov/pubmed/22216262
http://dx.doi.org/10.1371/journal.pone.0029367
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author Mueller, Henrik
Faé, Kellen C.
Magdorf, Klaus
Ganoza, Christian A.
Wahn, Ulrich
Guhlich, Ute
Feiterna-Sperling, Cornelia
Kaufmann, Stefan H. E.
author_facet Mueller, Henrik
Faé, Kellen C.
Magdorf, Klaus
Ganoza, Christian A.
Wahn, Ulrich
Guhlich, Ute
Feiterna-Sperling, Cornelia
Kaufmann, Stefan H. E.
author_sort Mueller, Henrik
collection PubMed
description BACKGROUND: Granulysin produced by cytolytic T cells directly contributes to immune defense against tuberculosis (TB). We investigated granulysin as a candidate immune marker for childhood and adolescent TB. METHODS: Peripheral blood mononuclear cells (PBMC) from children and adolescents (1–17 years) with active TB, latent TB infection (LTBI), nontuberculous mycobacteria (NTM) infection and from uninfected controls were isolated and restimulated in a 7-day restimulation assay. Intracellular staining was then performed to analyze antigen-specific induction of activation markers and cytotoxic proteins, notably, granulysin in CD4(+) CD45RO(+) memory T cells. RESULTS: CD4(+) CD45RO(+) T cells co-expressing granulysin with specificity for Mycobacterium tuberculosis (Mtb) were present in high frequency in TB-experienced children and adolescents. Proliferating memory T cells (CFSE(low)CD4(+)CD45RO(+)) were identified as main source of granulysin and these cells expressed both central and effector memory phenotype. PBMC from study participants after TB drug therapy revealed that granulysin-expressing CD4(+) T cells are long-lived, and express several activation and cytotoxicity markers with a proportion of cells being interferon-gamma-positive. In addition, granulysin-expressing T cell lines showed cytolytic activity against Mtb-infected target cells. CONCLUSIONS: Our data suggest granulysin expression by CD4(+) memory T cells as candidate immune marker for TB infection, notably, in childhood and adolescence.
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spelling pubmed-32464962012-01-03 Granulysin-Expressing CD4(+) T Cells as Candidate Immune Marker for Tuberculosis during Childhood and Adolescence Mueller, Henrik Faé, Kellen C. Magdorf, Klaus Ganoza, Christian A. Wahn, Ulrich Guhlich, Ute Feiterna-Sperling, Cornelia Kaufmann, Stefan H. E. PLoS One Research Article BACKGROUND: Granulysin produced by cytolytic T cells directly contributes to immune defense against tuberculosis (TB). We investigated granulysin as a candidate immune marker for childhood and adolescent TB. METHODS: Peripheral blood mononuclear cells (PBMC) from children and adolescents (1–17 years) with active TB, latent TB infection (LTBI), nontuberculous mycobacteria (NTM) infection and from uninfected controls were isolated and restimulated in a 7-day restimulation assay. Intracellular staining was then performed to analyze antigen-specific induction of activation markers and cytotoxic proteins, notably, granulysin in CD4(+) CD45RO(+) memory T cells. RESULTS: CD4(+) CD45RO(+) T cells co-expressing granulysin with specificity for Mycobacterium tuberculosis (Mtb) were present in high frequency in TB-experienced children and adolescents. Proliferating memory T cells (CFSE(low)CD4(+)CD45RO(+)) were identified as main source of granulysin and these cells expressed both central and effector memory phenotype. PBMC from study participants after TB drug therapy revealed that granulysin-expressing CD4(+) T cells are long-lived, and express several activation and cytotoxicity markers with a proportion of cells being interferon-gamma-positive. In addition, granulysin-expressing T cell lines showed cytolytic activity against Mtb-infected target cells. CONCLUSIONS: Our data suggest granulysin expression by CD4(+) memory T cells as candidate immune marker for TB infection, notably, in childhood and adolescence. Public Library of Science 2011-12-27 /pmc/articles/PMC3246496/ /pubmed/22216262 http://dx.doi.org/10.1371/journal.pone.0029367 Text en Mueller et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Mueller, Henrik
Faé, Kellen C.
Magdorf, Klaus
Ganoza, Christian A.
Wahn, Ulrich
Guhlich, Ute
Feiterna-Sperling, Cornelia
Kaufmann, Stefan H. E.
Granulysin-Expressing CD4(+) T Cells as Candidate Immune Marker for Tuberculosis during Childhood and Adolescence
title Granulysin-Expressing CD4(+) T Cells as Candidate Immune Marker for Tuberculosis during Childhood and Adolescence
title_full Granulysin-Expressing CD4(+) T Cells as Candidate Immune Marker for Tuberculosis during Childhood and Adolescence
title_fullStr Granulysin-Expressing CD4(+) T Cells as Candidate Immune Marker for Tuberculosis during Childhood and Adolescence
title_full_unstemmed Granulysin-Expressing CD4(+) T Cells as Candidate Immune Marker for Tuberculosis during Childhood and Adolescence
title_short Granulysin-Expressing CD4(+) T Cells as Candidate Immune Marker for Tuberculosis during Childhood and Adolescence
title_sort granulysin-expressing cd4(+) t cells as candidate immune marker for tuberculosis during childhood and adolescence
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3246496/
https://www.ncbi.nlm.nih.gov/pubmed/22216262
http://dx.doi.org/10.1371/journal.pone.0029367
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