Dynamics of T-cell IFN-γ and miR-29a expression during active pulmonary tuberculosis
Author(s) -
Anthony Afum-Adjei Awuah,
Bianca Ueberberg,
Ellis OwusuDabo,
Margaret Frempong,
Marc Jacobsen
Publication year - 2014
Publication title -
international immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.86
H-Index - 134
eISSN - 1460-2377
pISSN - 0953-8178
DOI - 10.1093/intimm/dxu068
Subject(s) - tuberculosis , mycobacterium tuberculosis , immunology , superantigen , interferon γ , chemotherapy , interferon , microrna , interferon gamma , t cell , virology , medicine , biology , immune system , gene , pathology , genetics
IFN-γ is crucial for protection against Mycobacterium tuberculosis. miR-29 was recently shown to non-redundantly inhibit IFN-γ. Here, we investigated IFN-γ and miR-29a expression dynamics of CD4(+) T cells from patients during active tuberculosis (TB) (n = 32) and in household contacts who were latently M. tuberculosis infected (n = 19) from Ghana. Whereas M. tuberculosis-specific IFN-γ expression was similar during TB chemotherapy, superantigen stimulation indicated generally impaired IFN-γ expression in TB patients. No interdependency between miR-29a and IFN-γ expression of T cells was observed. However, miR-29a was differentially expressed in T cells during chemotherapy. We concluded that differential miR-29a expression in active TB was not causative for impaired IFN-γ expression.
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