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Ras-associated small GTPase 33A, a novel T cell factor, is down-regulated in patients with tuberculosis
Department of Immunology, Max Planck Institute for Infection Biology, Berlin, Germany.
Institute for Medical Biometry and Statistics, University of Lübeck, Lübeck, Germany.ORCID-id: 0000-0002-7173-5579
Department of Immunology, Max Planck Institute for Infection Biology, Berlin, Germany.
Asklepios Center for Respiratory Medicine and Thoracic Surgery, Munich-Gauting, Germany .
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2005 (engelsk)Inngår i: Journal of Infectious Diseases, ISSN 0022-1899, E-ISSN 1537-6613, Vol. 192, nr 7, s. 1211-8Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Ras-associated small GTPases (Rabs) are specific regulators of intracellular vesicle trafficking. Interference with host cell vesicular transport is a hallmark of many intracellular pathogens, including the notable example Mycobacterium tuberculosis. We performed, by quantitative polymerase chain reaction, gene-expression analyses for selected Rab molecules in peripheral-blood mononuclear cells from patients with tuberculosis (TB) and healthy control subjects, to identify candidate genes that are critically involved in the host immune response. Comparison revealed significant differences in the expression of genes for Rab13, Rab24, and Rab33A. Rab33A gene expression was down-regulated in patients with TB and was predominantly expressed in CD8+ T cells. We excluded possible influences of differences in T cell percentages between the 2 study groups, demonstrating that Rab33A gene expression changes on the single-cell level. In vitro, Rab33A RNA expression was induced in T cells on activation and by dendritic cells infected with M. tuberculosis. Our findings identify Rab33A as a T cell regulatory molecule in TB and suggest its involvement in disease processes.

sted, utgiver, år, opplag, sider
Chicago, USA: University of Chicago Press, 2005. Vol. 192, nr 7, s. 1211-8
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Identifikatorer
URN: urn:nbn:se:oru:diva-40646DOI: 10.1086/444428ISI: 000231623700013PubMedID: 16136464Scopus ID: 2-s2.0-25444450362OAI: oai:DiVA.org:oru-40646DiVA, id: diva2:778048
Tilgjengelig fra: 2015-01-09 Laget: 2015-01-09 Sist oppdatert: 2018-01-30bibliografisk kontrollert

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