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Title: | FOXP3 Gene Expression in a Tuberculosis Case Contact Study |
Authors: | Burl, S. Hill, P. C. Jeffries, D. J. Holland, M. J. Fox, A. Lugos, M. D. Adegbola, R. A. Rook, G. A. Zumla, A. |
Keywords: | IL-10 T ᵣₑg |
Issue Date: | 2007 |
Publisher: | Clinical and Experimental Immunology |
Series/Report no.: | Vol.149;Pp 117–122 |
Abstract: | Regulatory T lymphocytes (Tregs) that express FOXP3 are involved in the
beneficial attenuation of immunopathology, but are also implicated in downregulation
of protective responses to infection. Their role in tuberculosis (TB)
is unknown.We classified 1272 healthy TB contacts according to their tuberculin
skin test (TST) and interferon (IFN)-g enzyme-linked immunospot
(ELISPOT) results and 128 TB cases, and studied the expression of FOXP3
and interleukin (IL)-10 in blood samples.Compared to the uninfected contact
group (TST–, ELISPOT–), we observed higher levels of FOXP3 mRNA in
blood from TB patients (< 0·001), but IL-10 expression was slightly lower
(P = 0·04). In contrast, FOXP3 expression levels were significantly lower
(P = 0·001) in the recently infected contacts (TST+, ELISPOT+) but there
was no difference for IL-10 (P = 0·74). We hypothesize that during early/
subclinical TB, most of which will become latent, FOXP3+ Tregs may be sequestered
in the lungs, but when TB becomes progressive, FOXP3 reappears at
increased levels in the periphery.While these findings do not reveal the role,
beneficial or harmful, of Tregs in TB, they emphasize the probable importance
of these cells. |
URI: | http://hdl.handle.net/123456789/1690 |
ISSN: | 1365-2249 |
Appears in Collections: | Medical Laboratory Sciences
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