Chronic viral infections are characterized by a state of T cell dysfunction that is associated with expression of the PD-1 (programmed cell death 1) inhibitory receptor. A better understanding of the mechanisms that regulate CD8 T cell responses during chronic viral infection is required to improve immunotherapies that restore function in exhausted CD8 T cells. We have recently identified a novel population of virus specific CD8 T cells that act as stem cells to maintain T cell responses during chronic infection of mice with lymphocytic choriomeningitis virus (LCMV). These stem-like LCMV specific CD8 T cells are found in the lymphoid tissues where they reside predominantly in the T cell zones along with nave CD8 T cells. They act as stem cells by undergoing a slow self-renewal and can also differentiate to give rise to the terminally differentiated CD8 T cells that are found at the major sites of infection in lymphoid as well as non-lymphoid tissues. Most importantly, the proliferative burst of T cells that is seen after PD-1 blockade comes almost exclusively from this stem-like CD8 T cell subset. Our studies have been confirmed and extended by others who have found similar CD8 T cells in other chronic viral infections of mice and also in chronic infections of non-human primates and humans. The studies proposed in the application are now focused on understanding how these virus specific stem-like CD8 T cells are generated and maintained during chronic infection and how this information can be used to develop rational approaches for optimizing PD-1 directed immunotherapy. The following specific aims are proposed to achieve these goals:
Specific aim 1 : To understand how the generation and maintenance of virus specific stem-like CD8 T cells is regulated during chronic viral infection.
Specific aim 2 : To develop strategies for enhancing virus specific stem-like CD8 T cells and optimizing PD-1 directed immunotherapy.

Public Health Relevance

Memory CD8 T cells are an essential component of protective immunity, and generating effective memory CD8 T cell populations with large quantity and superior quality is a major goal of successful vaccines against chronic viral infections. Uncovering the mechanisms that give us a better understanding of the memory T cell populations during chronic viral infection could lead to establishing new and more specific molecular targets for vaccine development and chronic viral control. !

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI030048-26
Application #
9647402
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Repik, Patricia M
Project Start
1990-07-01
Project End
2023-02-28
Budget Start
2019-03-01
Budget End
2020-02-29
Support Year
26
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Emory University
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
066469933
City
Atlanta
State
GA
Country
United States
Zip Code
30322
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