Vaccine efficacy depends on strong long-term development of immune memory. CD8+ T cells play critical roles in the immune response to bacteria and viruses, and the development of an effective CD8+ T cell immune response has been intensely investigated. Memory CD8+ T cells develop following antigenic responses over several identifiable phases. Initial antigen or pathogen recognition initiates clonal expansion of nave T cells, which develop into effector T cells. Upon pathogen or antigen clearance, these effector T cells undergo a drastic contraction phase, with death of a majority of the effector cell, and the development of memory precursor effector cells, which proceed to differentiate into memory T cells. Methods to selectively manipulate this process would greatly enhance tuning the immune response in specific conditions. However, this process is still poorly understood. Three parameters that affect these responses are antigen affinity, T cell receptor (TcR) signal strength and inflammation. Antigen affinity (for TcR) and TcR signal are T cell intrinsic, while inflammation is thought to be T cell extrinsic. How these three parameters intersect to control memory development is unclear. The tyrosine kinase Itk is a pharmaceutically tractable target that regulates TcR signal strength, and our preliminary data suggest that it tunes T cell mediated inflammation, and timing of the development CD8+ memory T cell response. The objective of this application is to determine the role of Itk regulated TcR signal strength and antigen affinity for TcR, in tuning the development of CD8+ effector and memory responses during bacterial infection. We will test the hypothesis that pathways regulated by Itk tune inflammation during CD8+ T cell response, regulating the development of memory CD8+ T cells in response to infection.
Our specific aims are: 1) Determine the ability of TCR signal strength to tune antigen affinity induced development of short-term effector and long term memory CD8+ T cells during infection; 2) Determine the mechanism by which of Itk regulates development of MPEC during infection induced memory generation, and 3) Determine the ability of Itk to tune inflammation and thus the development of short-term effector and long-term memory CD8+ T cells during infection. This work is extremely innovative as we have exciting preliminary data that when fleshed out, will provide information on a signaling pathway that could be manipulated to enhance the development of memory T cells, while reducing vaccine induced inflammation. This work is also innovative because we have devised novel approaches to study the impact of this signaling pathway on the development of different phases of the CD8+ T cell response. Furthermore, our work is highly translatable as it could lead to a method to tune the development of CD8+ T cell memory in humans.

Public Health Relevance

The timing and magnitude of the T cell response is important in controlling vaccine efficiency. The affinity of the antigen for T cell receptors, as well as the strength of signal via those receptors are parameters that can control this response. However, how these two parameters intersect to control the development of T cell immune memory is unclear. This work will determine how antigen affinity and TcR signal strength intersect to tune the inflammatory environment and thus the timing and magnitude of the T cell response, allowing controllable tuning of memory development and vaccine efficiency.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI120701-03
Application #
9485864
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Mallia, Conrad M
Project Start
2016-06-24
Project End
2020-05-31
Budget Start
2018-06-01
Budget End
2019-05-31
Support Year
3
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Cornell University
Department
Microbiology/Immun/Virology
Type
Schools of Veterinary Medicine
DUNS #
872612445
City
Ithaca
State
NY
Country
United States
Zip Code
14850
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Huang, Weishan; Solouki, Sabrina; Koylass, Nicholas et al. (2017) ITK signalling via the Ras/IRF4 pathway regulates the development and function of Tr1 cells. Nat Commun 8:15871
Kannan, Arun K; Mohinta, Sonia; Huang, Weishan et al. (2017) T-Bet independent development of IFN? secreting natural T helper 1 cell population in the absence of Itk. Sci Rep 7:45935