Cryptococcus neoformans is a common cause of fatal fungal infection in patients with AIDS. The respiratory tract is the portal of entry for this ubiquitous, encapsulated yeast and the development of protective Th1 cell-mediated immunity (CMI) is crucial to eradicate the organism and control cryptococcal dissemination from the lungs to the brain. Production of cytokines and other mediators by cells of the innate immune system direct the development of CMI, but the precise nature of these early cellular and molecular events remains to be determined. CCR2 and other chemokine receptors (CKRs) have recently been identified as important co-factors for HIV infections and therapies aimed at blocking CKR binding are being considered. It is of considerable importance to understand the role of CKRs in host defense against infection by AIDS-associated pathogens because CKR antagonists will likely be used in patients concurrently infected with one or more of these pathogens. We have identified in preliminary studies with CCR2 knockout mice that protective Th1 immunity against C. neoformans cannot develop in the absence of CCR2 even if CD4+ and CD8+ T cell numbers in the lungs, blood, and spleen are normal. Hypothesis: MCP-1 via CCR2 mediates mononuclear cell co-stimulation and recruitment which is required to develop protective Th1 immunity against C. neoformans; deficient CCR2 function results in Th2 immunity and an inability to clear C. neoformans.
Specific Aims : (1) To identify the cells in the lungs that express CCR2 during C. neoformans infection; (2) to determine the role of the CCR2 ligand MCP-1 in the development of Th1 immunity to C. neoformans; (3) to determine the role of CCR2 in the activation and recruitment of macrophages during pulmonary C. neoformans infection; (4) to determine the role of CCR2 in the recruitment and activation of T cells during pulmonary C. neoformans infection; (5) To determine the role of MCP-1 and CCR2 in the development of a Th2 response to C. neoformans.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL063670-04
Application #
6537703
Study Section
Special Emphasis Panel (ZHL1-CSR-H (M2))
Program Officer
Colombini-Hatch, Sandra
Project Start
1999-07-02
Project End
2004-06-30
Budget Start
2002-07-01
Budget End
2003-06-30
Support Year
4
Fiscal Year
2002
Total Cost
$262,751
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
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Zhang, Yanmei; Wang, Fuyuan; Bhan, Urvashi et al. (2010) TLR9 signaling is required for generation of the adaptive immune protection in Cryptococcus neoformans-infected lungs. Am J Pathol 177:754-65
Zhang, Yanmei; Wang, Fuyuan; Tompkins, Kristin C et al. (2009) Robust Th1 and Th17 immunity supports pulmonary clearance but cannot prevent systemic dissemination of highly virulent Cryptococcus neoformans H99. Am J Pathol 175:2489-500
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Noverr, Mairi C; Erb-Downward, John R; Huffnagle, Gary B (2003) Production of eicosanoids and other oxylipins by pathogenic eukaryotic microbes. Clin Microbiol Rev 16:517-33

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