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Maturation and mip-1β production of cytomegalovirus-specific T cell responses in Tanzanian children, adolescents and adults : impact by HIV and Mycobacterium tuberculosis co-infections
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 3122580
Author(s) Portevin, Damien; Moukambi, Félicien; Mpina, Maxmillian; Bauer, Asli; Haraka, Frederick; Chachage, Mkunde; Metzger, Philipp; Saathoff, Elmar; Clowes, Petra; Ntinginya, Nyanda E.; Rachow, Andrea; Hoelscher, Michael; Reither, Klaus; Daubenberger, Claudia A.; Geldmacher, Christof
Author(s) at UniBasel Portevin, Damien
Daubenberger, Claudia
Reither, Klaus
Year 2015
Title Maturation and mip-1β production of cytomegalovirus-specific T cell responses in Tanzanian children, adolescents and adults : impact by HIV and Mycobacterium tuberculosis co-infections
Journal PLoS ONE
Volume 10
Number 5
Pages / Article-Number e0126716
Mesh terms Adolescent; Adult; Age Factors; CD4-Positive T-Lymphocytes, virology; CD8-Positive T-Lymphocytes, virology; Chemokine CCL4, metabolism; Child; Cohort Studies; Coinfection, immunology; Cytomegalovirus, immunology; Cytomegalovirus Infections, virology; HIV Infections, immunology; Humans; Interferon-gamma, metabolism; Male; Phosphoproteins, metabolism; Risk Factors; Tanzania; Tuberculosis, immunology; Tumor Necrosis Factor Receptor Superfamily, Member 7, metabolism; Viral Matrix Proteins, metabolism; Young Adult
Abstract It is well accepted that aging and HIV infection are associated with quantitative and functional changes of CMV-specific T cell responses. We studied here the expression of Mip-1β and the T cell maturation marker CD27 within CMVpp65-specific CD4+ and CD8+ T cells in relation to age, HIV and active Tuberculosis (TB) co-infection in a cohort of Tanzanian volunteers (≤16 years of age, n = 108 and ≥18 years, n = 79). Independent of HIV co-infection, IFNγ+ CMVpp65-specific CD4+ T cell frequencies increased with age. In adults, HIV co-infection further increased the frequencies of these cells. A high capacity for Mip-1β production together with a CD27low phenotype was characteristic for these cells in children and adults. Interestingly, in addition to HIV co-infection active TB disease was linked to further down regulation of CD27 and increased capacity of Mip-1β production in CMVpp65-specific CD4+ T cells. These phenotypic and functional changes of CMVpp65-specific CD4 T cells observed during HIV infection and active TB could be associated with increased CMV reactivation rates.
Publisher Public Library of Science
ISSN/ISBN 1932-6203
edoc-URL http://edoc.unibas.ch/dok/A6381866
Full Text on edoc Available
Digital Object Identifier DOI 10.1371/journal.pone.0126716
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/25974183
Document type (ISI) Journal Article
 
   

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