A study of the thymus-leukemia (TL) antigens' amino acid sequence lends credence to the hypothesis that TL proteins may possess an antigen binding cleft similar to that found on the paradigmatic HLA-A2 class I glycoprotein. Like HLA-A2, but in a far more restricted manner, the TL molecules may be capable of binding and presenting antigen. In this context, recent reports have implicated TL as the antigen presenting ligand for gamma/delta T cell receptor (TcR) molecules. Thus, the long-term objectives of this proposal are to understand both the biological function of the TL family of class I genes and proteins as well as the molecular mechanisms which regulate the genes' tissue-specific expression. Specifically, transgenic mice will be produced and used to study the pattern of expression of TL driven by the H-2Kb promoter. Initial experiments have demonstrated that the gene is expressed in such mice similar to endogenous H-2 class I proteins. Antibodies against TcR, CD4, and CD8 molecules will first be used to stain transgenic immune cells in order to determine whether ectopic expression of TL results in the perturbation of T cell differentiative pathways. Immunologically, TL will be assessed for its ability to serve as a transplantation antigen and a CTL restriction element using virus models. Positive results will allow for the cloning of the effector T cells and an examination of their TcR molecules. Such results can yield an indication as to the ligand with which TL interacts in vivo as well as TL's possible functional role. These experiments can also form the basis for future structure-function studies. Experiments involving the analysis of novel mAb antibodies putatively reacting with TL peptides derived from unspliced TL transcripts as well as the identification of TL promoter elements involved in splicing and tissue-specific TL expression will be continued.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
1R01CA053445-01A1
Application #
3198153
Study Section
Immunobiology Study Section (IMB)
Project Start
1991-06-14
Project End
1994-05-31
Budget Start
1991-06-14
Budget End
1992-05-31
Support Year
1
Fiscal Year
1991
Total Cost
Indirect Cost
Name
Pennsylvania State University
Department
Type
Schools of Medicine
DUNS #
129348186
City
Hershey
State
PA
Country
United States
Zip Code
17033
Sharma, P; Page, M J; Poritz, L S et al. (1997) An increased gamma delta T cell population in the intestine of thymus-leukemia antigen transgenic mice. Cell Immunol 176:153-7
Sharma, P; Joyce, S; Chorney, K A et al. (1996) Thymus-leukemia antigen interacts with T cells and self-peptides. J Immunol 156:987-96
Sharma, P; Johnson, C A; Bonneau, R H et al. (1996) Transgenic mice expressing the thymus leukemia antigen fail to control cutaneous herpes simplex virus infection. Cell Immunol 174:84-9