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Distinct, Specific IL-17- and IL-22-Producing CD4+ T Cell Subsets Contribute to the Human Anti-Mycobacterial Immune Response
Author(s) -
Thomas J. Scriba,
Barbara Kalsdorf,
Deborah-Ann Abrahams,
Fatima Isaacs,
Jessica Hofmeister,
Gillian F. Black,
Hisham Y. Hassan,
Robert J. Wilkinson,
Gerhard Walzl,
Sebastian Gelderbloem,
Hassan Mahomed,
Gregory Hussey,
Willem A. Hanekom
Publication year - 2008
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.180.3.1962
Subject(s) - immune system , immunology , cytokine , proinflammatory cytokine , biology , t cell , peripheral blood mononuclear cell , interleukin 4 , bronchoalveolar lavage , in vitro , interleukin , interleukin 10 , inflammation , medicine , lung , biochemistry
We investigated whether the proinflammatory T cell cytokines IL-17 and IL-22 are induced by human mycobacterial infection. Remarkably, >20% of specific cytokine-producing CD4(+) T cells in peripheral blood of healthy, mycobacteria-exposed adults expressed IL-17 or IL-22. Specific IL-17- and IL-22-producing CD4(+) T cells were distinct from each other and from Th1 cytokine-producing cells. These cells had phenotypic characteristics of long-lived central memory cells. In patients with tuberculosis disease, peripheral blood frequencies of these cells were reduced, whereas bronchoalveolar lavage fluid contained higher levels of IL-22 protein compared with healthy controls. IL-17 was not detected in this fluid, which may be due to suppression by Th1 cytokines, as PBMC IL-17 production was inhibited by IFN-gamma in vitro. However, Th1 cytokines had no effect on IL-22 production in vitro. Our results imply that the magnitude and complexity of the anti-mycobacterial immune response have historically been underestimated. IL-17- and IL-22-producing CD4(+) T cells may play important roles in the human immune response to mycobacteria.

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