Aging, T cell repertoire, and cellular immunity to influenza virus

Information

  • Research Project
  • 8307776
  • ApplicationId
    8307776
  • Core Project Number
    R01AG039485
  • Full Project Number
    5R01AG039485-02
  • Serial Number
    039485
  • FOA Number
    PA-10-067
  • Sub Project Id
  • Project Start Date
    8/1/2011 - 13 years ago
  • Project End Date
    5/31/2016 - 8 years ago
  • Program Officer Name
    FULDNER, REBECCA A.
  • Budget Start Date
    6/15/2012 - 12 years ago
  • Budget End Date
    5/31/2013 - 11 years ago
  • Fiscal Year
    2012
  • Support Year
    02
  • Suffix
  • Award Notice Date
    6/8/2012 - 12 years ago
Organizations

Aging, T cell repertoire, and cellular immunity to influenza virus

DESCRIPTION (provided by applicant): Immune function declines with age, resulting in increased susceptibility of aged individuals to infection and impaired responses to vaccines. A key focus of the current proposal is to use a well-characterized mouse model of influenza virus infection to determine mechanisms underlying the decreased ability of aged individuals to respond to and develop memory to new infections and vaccination. These studies are essential in order to develop strategies for overcoming these defects. The ability to generate T cell responses to newly encountered antigens and to respond to vaccination is dependent on the maintenance of a diverse repertoire of T cells. We have previously shown that there is an age-associated reduction in repertoire diversity among CD8 T cells, which has profound consequences for primary and protective immunity to influenza virus. Because of reduced numbers and diversity of naive T cells in aged individuals, we hypothesize that aging results in a greater contribution of fortuitously cross-reactive memory cells to the response to new infections, and that this will lead to stochastic responses, often of lower avidity, and perhaps detrimental or pathological. In support of this, we have preliminary data showing that fortuitously cross-reactive memory cells from influenza-naive aged mice can respond to influenza virus epitopes, and in Aim 1 we will determine the contribution of cross reactive memory to the response to new infections, and assess the implications for cellular immunity. Two additional well-characterized defects associated with aging are that CD4 T cells are functionally impaired and that poor CD8 T cell memory is generated. However, the contribution of aged CD4 T cells to the development of defective CD8 memory is an understudied area in aging research, and will be examined in Aim 2 of the proposal. Taken together, these studies will address mechanisms underlying the age-associated decline in cellular immunity which is essential for the goal of designing better therapies and vaccines for elderly humans.

IC Name
NATIONAL INSTITUTE ON AGING
  • Activity
    R01
  • Administering IC
    AG
  • Application Type
    5
  • Direct Cost Amount
    102500
  • Indirect Cost Amount
    90200
  • Total Cost
    192700
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    866
  • Ed Inst. Type
  • Funding ICs
    NIA:192700\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    ASG
  • Study Section Name
    Aging Systems and Geriatrics Study Section
  • Organization Name
    TRUDEAU INSTITUTE, INC.
  • Organization Department
  • Organization DUNS
    020658969
  • Organization City
    SARANAC LAKE
  • Organization State
    NY
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    129832100
  • Organization District
    UNITED STATES