This proposal is focused upon the intracellular amastigote stage of Leishmania parasites. Disease pathology associated with infection is due to mechanisms of and response by the host to the amastigote stage of the parasite. Research during the past period of support has demonstrated that immunization with molecules specifically expressed or upregulated in the amastigote stage can confer resistance to infection. Interestingly, recent data indicate that amastigotes residing within the macrophage parasitophorous vacuole can sequester their antigens from MHC class II presentation (CD4+ T cells). However, CD8+ (as well as CD4+) T cells are critical resistance/protection against infection in immunized/vaccinated C57BL/6 mice. Consequently, the hypothesis to be examined in this proposal is that: CD8 T cells are important in vaccinated (immune) mice for protection against infection. This hypothesis will be examined using mice of different genetic background (susceptibility to infection) and both protective and non-protective antigens. Further, the CD8 T cell mechanisms potentially contributing to protection and their effect on CD4 T cell activation will be explored. The contributions of CTL activity and of TC1 versus TC2 CD8+ T cells will be examined. The ability of CD8+ T cells to amplify and/or modulate the CD4+ response [TCR usage; cytokine profile] will be determined. In addition, the biological roles of the protective amastigote antigens [P-4 and P-8] will be investigated. These studies will focus on the Leishmania mexicana complex.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
2R01AI027811-09A1
Application #
2462853
Study Section
Tropical Medicine and Parasitology Study Section (TMP)
Project Start
1989-04-01
Project End
2002-01-31
Budget Start
1998-02-01
Budget End
1999-01-31
Support Year
9
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Yale University
Department
Public Health & Prev Medicine
Type
Schools of Medicine
DUNS #
082359691
City
New Haven
State
CT
Country
United States
Zip Code
06520
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Deak, Eszter; Jayakumar, Asha; Cho, Ka Wing et al. (2010) Murine visceral leishmaniasis: IgM and polyclonal B-cell activation lead to disease exacerbation. Eur J Immunol 40:1355-68
Matza, Didi; Badou, Abdallah; Kobayashi, Koichi S et al. (2008) A scaffold protein, AHNAK1, is required for calcium signaling during T cell activation. Immunity 28:64-74
Carrillo, E; Ahmed, S; Goldsmith-Pestana, K et al. (2007) Immunogenicity of the P-8 amastigote antigen in the experimental model of canine visceral leishmaniasis. Vaccine 25:1534-43