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Interleukin-10 Promotes Mycobacterium tuberculosis Disease Progression in CBA/J Mice
Author(s) -
Gillian Beamer,
David K. Flaherty,
Barnabe Dossou Assogba,
Paul C. Stromberg,
Mercedes GonzalezJuarrero,
René de Waal Malefyt,
Bridget Vesosky,
Joanne Turner
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.181.8.5545
Subject(s) - mycobacterium tuberculosis , tuberculosis , microbiology and biotechnology , biology , virology , medicine , pathology
IL-10 is a potent immunomodulatory cytokine that affects innate and acquired immune responses. The immunological consequences of IL-10 production during pulmonary tuberculosis (TB) are currently unknown, although IL-10 has been implicated in reactivation TB in humans and with TB disease in mice. Using Mycobacterium tuberculosis-susceptible CBA/J mice, we show that blocking the action of IL-10 in vivo during chronic infection stabilized the pulmonary bacterial load and improved survival. Furthermore, this beneficial outcome was highly associated with the recruitment of T cells to the lungs and enhanced T cell IFN-gamma production. Our results indicate that IL-10 promotes TB disease progression. These findings have important diagnostic and/or therapeutic implications for the prevention of reactivation TB in humans.

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