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    CD8 T cell cross-reactivity networks mediate heterologous immunity in human EBV and murine vaccinia virus infections

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    Authors
    Cornberg, Markus
    Clute, Shalyn Catherine
    Watkin, Levi B.
    Saccoccio, Frances M.
    Kim, Sung-Kwon
    Naumov, Yuri N.
    Brehm, Michael A.
    Aslan, Nuray
    Welsh, Raymond M.
    Selin, Liisa K.
    Student Authors
    Levi B. Watkin
    UMass Chan Affiliations
    Department of Pathology
    Document Type
    Journal Article
    Publication Date
    2010-03-15
    Keywords
    Adolescent; Adoptive Transfer; Animals; CD8-Positive T-Lymphocytes; Cell Line, Tumor; Cells, Cultured; Coculture Techniques; Epitopes, T-Lymphocyte; Epstein-Barr Virus Infections; Humans; Immunity, Cellular; Immunologic Memory; Influenza, Human; Lymphocyte Activation; Lymphocytic Choriomeningitis; Male; Mice; Mice, Congenic; Mice, Inbred C57BL; Vaccinia; Young Adult
    Immunology and Infectious Disease
    Life Sciences
    Medicine and Health Sciences
    
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    Link to Full Text
    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253758/
    Abstract
    In this study, we demonstrate complex networks of CD8 T cell cross-reactivities between influenza A virus and EBV in humans and between lymphocytic choriomeningitis virus and vaccinia virus in mice. We also show directly that cross-reactive T cells mediate protective heterologous immunity in mice. Subsets of T cell populations reactive with one epitope cross-reacted with either of several other epitopes encoded by the same or the heterologous virus. Human T cells specific to EBV-encoded BMLF1(280-288) could be cross-reactive with two influenza A virus or two other EBV epitopes. Mouse T cells specific to the vaccinia virus-encoded a11r(198-205) could be cross-reactive with three different lymphocytic choriomeningitis virus, one Pichinde virus, or one other vaccinia virus epitope. Patterns of cross-reactivity differed among individuals, reflecting the private specificities of the host's immune repertoire and divergence in the abilities of T cell populations to mediate protective immunity. Defining such cross-reactive networks between commonly encountered human pathogens may facilitate the design of vaccines.
    Source

    J Immunol. 2010 Mar 15;184(6):2825-38. Epub 2010 Feb 17.

    DOI
    10.4049/jimmunol.0902168
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/33243
    PubMed ID
    20164414
    Related Resources

    Link to article in PubMed

    ae974a485f413a2113503eed53cd6c53
    10.4049/jimmunol.0902168
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