Cytotoxic T lymphocytes (CTL) are likely to play an important role in limiting the spread of the human immunodeficiency virus (HIV) in infected individuals. This cellular immune response will be studied in simian immunodeficiency virus (SIV)-infected rhesus monkeys. In these studies we will assess: I. SIV CTL epitopes and restricting MHC class I molecules in rhesus monkeys. II. T cell receptor V gene usage in SIV-infected monkeys. III. The role of CTL pressure in the selection of SIV mutations. IV. Novel vaccine approaches for the generation of SIV-specific CTL. V. The contribution of CTL in the control SIV spread during primary infection.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
2R37AI020729-10
Application #
3481133
Study Section
AIDS and Related Research Study Section 1 (ARRA)
Project Start
1983-09-15
Project End
1997-11-30
Budget Start
1992-12-01
Budget End
1993-11-30
Support Year
10
Fiscal Year
1993
Total Cost
Indirect Cost
Name
Harvard University
Department
Type
Schools of Medicine
DUNS #
082359691
City
Boston
State
MA
Country
United States
Zip Code
02115
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LaBonte, Michelle L; McKay, Paul F; Letvin, Norman L (2006) Evidence of NK cell dysfunction in SIV-infected rhesus monkeys: impairment of cytokine secretion and NKG2C/C2 expression. Eur J Immunol 36:2424-33
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