Numerous studies have demonstrated the regulatory capability of peptide/MHC determinant density on T lymphocytes. In particular, we have shown that the avidity of a CTL population can be controlled by the amount of antigen presented on the APC and that avidity is a property that significantly affects the ability of the CTL to clear virus in vivo. Little is known about the way in which avidity is controlled in CTL. The goal of these studies is to define the cell surface molecules involved in determination of CTL avidity. This goal will be sought by evaluating the TCR usage, the requirement for costimulation, and the helper dependence of high versus low avidity CTL. The role of the TCR in determining avidity will be assessed in high and low avidity CTL by precursor frequency and Vbeta/Valpha analysis and by analysis of non-TCR factors controlling avidity in CTL of various avidity generated using a common TCR. The efficiency of various APC populations to activate high versus low avidity CTL will be analyzed. These APC populations possess diverse costimulatory molecules that may be differentially required by high and low avidity CTL. To further investigate the requirement for costimulatory molecules, the dependence on CD28 and CTLA4 signals will be evaluated. Finally the requirement for exogenous cytokines provided by CD4+ helper cells will be determined by generation of high and low avidity CTL in vitro in the absence of added growth factors and in vivo by elicitation in the absence of CD4+ cells. At the conclusion of these studies, we should gain new insights in the ways in which peptide/MHC determinant density regulates CD8+ cytotoxic T lymphocytes. Specifically we should understand more fully the repertoire of precursors available for response to a particular antigenic peptide, the contribution of the TCR to the avidity of an individual CTL, and the effect of signals provided by costimulatory molecules and cytokines on the activation and proliferation of CTL of defined avidity. These findings may contribute to the development of improved immunotherapeutic and vaccination strategies in which the selective activation or deletion of CTL possessing a defined avidity would be beneficial.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
6R01AI043591-05
Application #
6632130
Study Section
Immunobiology Study Section (IMB)
Program Officer
Chiodetti, Lynda
Project Start
1999-03-01
Project End
2005-02-28
Budget Start
2003-03-01
Budget End
2005-02-28
Support Year
5
Fiscal Year
2003
Total Cost
$220,204
Indirect Cost
Name
Wake Forest University Health Sciences
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
937727907
City
Winston-Salem
State
NC
Country
United States
Zip Code
27157
Holbrook, Beth C; Yammani, Rama D; Blevins, Lance K et al. (2013) In vivo modulation of avidity in highly sensitive CD8(+) effector T cells following viral infection. Viral Immunol 26:302-13
Amoah, Samuel; Holbrook, Beth C; Yammani, Rama D et al. (2013) High viral burden restricts short-lived effector cell number at late times postinfection through increased natural regulatory T cell expansion. J Immunol 190:5020-9
Amoah, Samuel; Yammani, Rama D; Grayson, Jason M et al. (2012) Changes in functional but not structural avidity during differentiation of CD8+ effector cells in vivo after virus infection. J Immunol 189:638-45
Sharma, Sharad K; Alexander-Miller, Martha A (2011) Increased sensitivity to antigen in high avidity CD8(+) T cells results from augmented membrane proximal T-cell receptor signal transduction. Immunology 133:307-17
Kroger, Charles J; Amoah, Samuel; Alexander-Miller, Martha A (2008) Cutting edge: Dendritic cells prime a high avidity CTL response independent of the level of presented antigen. J Immunol 180:5784-8
Kroger, Charles J; Alexander-Miller, Martha A (2007) Dose-dependent modulation of CD8 and functional avidity as a result of peptide encounter. Immunology 122:167-78
Kroger, Charles J; Alexander-Miller, Martha A (2007) Cutting edge: CD8+ T cell clones possess the potential to differentiate into both high- and low-avidity effector cells. J Immunol 179:748-51
Gray, Peter M; Arimilli, Subhashini; Palmer, Ellen M et al. (2005) Altered function in CD8+ T cells following paramyxovirus infection of the respiratory tract. J Virol 79:3339-49
Cawthon, Andrew G; Kroger, Charles J; Alexander-Miller, Martha A (2004) High avidity CD8+ T cells generated from CD28-deficient or wildtype mice exhibit a differential dependence on lipid raft integrity for activation. Cell Immunol 227:148-55
Gray, Peter M; Parks, Griffith D; Alexander-Miller, Martha A (2003) High avidity CD8+ T cells are the initial population elicited following viral infection of the respiratory tract. J Immunol 170:174-81

Showing the most recent 10 out of 14 publications