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A more recent version of this article appeared on June 1, 2005

Published online before print March 14, 2005
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© by The Society for Leukocyte Biology
Journal of Leukocyte Biology, doi:10.1189/jlb.1204723


Received for publication December 13, 2004.
Revised January 25, 2005.
Accepted for publication February 3, 2005.


Article

Disruption of granulocyte macrophage-colony stimulating factor production in the lungs severely affects the ability of mice to control Mycobacterium tuberculosis infection

Mercedes Gonzalez-Juarrero *@, Jessica M. Hattle *, Angelo Izzo *, Ana Paula Junquiera-Kipnis *, Tae S. Shim *, Bruce C. Trapnell {dagger}, Andrea M. Cooper {ddagger}, and Ian M. Orme *

*Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins; {dagger}Division of Pulmonary Biology, Children’s Hospital Research Foundation, University of Cincinnati, Ohio; and {ddagger}Trudeau Institute, Saranac Lake, New York

@ To whom correspondence should be addressed. E-mail: malba{at}lamar.colostate.edu.


   Abstract

Mice lacking expression of granulocyte macrophage-colony stimulating factor knockout (GM-CSF KO) are unable to contain Mycobacterium tuberculosis growth and succumb to infection by 35 days following pulmonary challenge. GM-CSF KO mice do not express normal levels of the inflammatory cytokine tumor necrosis factor {alpha} (TNF-{alpha}) nor the chemokines, regulated on activation, normal T expressed and secreted (RANTES), macrophage-inflammatory protein-1{beta} (MIP-1{beta}), MIP-1{alpha}, and lymphotactin, which are required for recruitment of lymphocytes and expression of a T helper cell type 1 (TH1) response within the lungs. In contrast, transgenic mice overexpressing GM-CSF in the lungs but with a lack of GM-CSF in other organs (GM+) are able to recruit lymphocytes and to express a TH1 response with production of TNF-{alpha} and interferon-{gamma} in the lungs. However, GM+ mice succumb to infection between 60 and 90 days post-challenge, as they are unable to develop a normal granulomatous response. Although GM+ mice are able to express the chemokine RANTES, they lack the ability to express other inflammatory chemokines such as lymphotactin and MIP-1{beta}. We conclude that GM-CSF is essential to the recruitment of lymphocytes and expression of a TH1 response in the lung, to the generation of a normal mononuclear granuloma, and most importantly, to the containment of M. tuberculosis bacterial growth.

Key Words: GM-CSF • cytokines • chemokines • granuloma




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