This is a clinical and laboratory program designed to study the mechanism of cell mediated immunity (CMI) and how it is subverted in leprosy. In particular we will define the role of key cytokines in regulating the mechanisms necessary to mount a protective response to M. leprae infection. For this purpose we will examine the phenotypic and functional characteristics of T cells, monocytes and NK/LAK cells in the blood and after migration into the lesions as well as resident endothelial cells, Langerhans cells and keratinocytes. Using immunocytochemistry, election microscopy, cell proliferation, activation and cytotoxicity assays as well as Northern blotting, ELISA and quantitative PCR, we will evaluate the nature, interactions and secretory repertoire of cells which accumulate in lepromatous, tuberculoid and reactional patients skin. The ability of recombinant cytokines such as IL-2 and IFN-gamma to modify host cells function and dispose of M. leprae in situ will be compared with the generation and function of cytotoxic cells reactive against infected monocytes in vitro. The role of cytokines and leukocyte activation in the pathobiology of the reactional states including erythema nodosum leprosum and reversal reaction will be dissected. How cytokines including GM-CSF impact on tissue damage and wound healing in the skin of leprosy patients will be studied. And finally how the HIV-1 pandemic will affect the incidence and clinical progression of leprosy will be investigated. Each of these modalities will be followed temporally, in selected patient populations, obtained through collaborative efforts in Brazil and the Philippines. The work is an extension of the achievements reported in the prior grant period.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
2R01AI022616-09
Application #
2061900
Study Section
Biological Sciences 2 (BIOL)
Project Start
1986-04-01
Project End
1998-12-31
Budget Start
1994-04-01
Budget End
1994-12-31
Support Year
9
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Rockefeller University
Department
Other Basic Sciences
Type
Other Domestic Higher Education
DUNS #
071037113
City
New York
State
NY
Country
United States
Zip Code
10065
Berrington, William Richard; Macdonald, Murdo; Khadge, Saraswoti et al. (2010) Common polymorphisms in the NOD2 gene region are associated with leprosy and its reactive states. J Infect Dis 201:1422-35
Sapkota, Bishwa R; Macdonald, Murdo; Berrington, William R et al. (2010) Association of TNF, MBL, and VDR polymorphisms with leprosy phenotypes. Hum Immunol 71:992-8
Bochud, P-Y; Sinsimer, D; Aderem, A et al. (2009) Polymorphisms in Toll-like receptor 4 (TLR4) are associated with protection against leprosy. Eur J Clin Microbiol Infect Dis 28:1055-65
Reich-Slotky, Ronit; Kabbash, Christina A; Della-Latta, Phyllis et al. (2009) Gemfibrozil inhibits Legionella pneumophila and Mycobacterium tuberculosis enoyl coenzyme A reductases and blocks intracellular growth of these bacteria in macrophages. J Bacteriol 191:5262-71
Murray, Rose Ann; Siddiqui, Mahveen Ruby; Mendillo, Megan et al. (2007) Mycobacterium leprae inhibits dendritic cell activation and maturation. J Immunol 178:338-44
Davids, Virginia; Hanekom, Willem; Gelderbloem, Sebastian J et al. (2007) Dose-dependent immune response to Mycobacterium bovis BCG vaccination in neonates. Clin Vaccine Immunol 14:198-200