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10.1016/j.immuni.2014.09.007

http://scihub22266oqcxt.onion/10.1016/j.immuni.2014.09.007
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suck abstract from ncbi


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pmid25308332
      Immunity 2014 ; 41 (4 ): 633-45
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  • CD4+ T cell help guides formation of CD103+ lung-resident memory CD8+ T cells during influenza viral infection #MMPMID25308332
  • Laidlaw BJ ; Zhang N ; Marshall HD ; Staron MM ; Guan T ; Hu Y ; Cauley LS ; Craft J ; Kaech SM
  • Immunity 2014[Oct]; 41 (4 ): 633-45 PMID25308332 show ga
  • Tissue-resident memory T (Trm) cells provide enhanced protection against infection at mucosal sites. Here we found that CD4(+) T cells are important for the formation of functional lung-resident CD8(+) T cells after influenza virus infection. In the absence of CD4(+) T cells, CD8(+) T cells displayed reduced expression of CD103 (Itgae), were mislocalized away from airway epithelia, and demonstrated an impaired ability to recruit CD8(+) T cells to the lung airways upon heterosubtypic challenge. CD4(+) T cell-derived interferon-? was necessary for generating lung-resident CD103(+) CD8(+) Trm cells. Furthermore, expression of the transcription factor T-bet was increased in "unhelped" lung Trm cells, and a reduction in T-bet rescued CD103 expression in the absence of CD4(+) T cell help. Thus, CD4(+) T cell-dependent signals are important to limit expression of T-bet and allow for the development of CD103(+) CD8(+) Trm cells in the lung airways following respiratory infection.
  • |*Immunologic Memory [MESH]
  • |Animals [MESH]
  • |Antigens, CD/immunology [MESH]
  • |CD4-Positive T-Lymphocytes/*immunology [MESH]
  • |CD8-Positive T-Lymphocytes/*immunology [MESH]
  • |Influenza A Virus, H3N2 Subtype/*immunology [MESH]
  • |Integrin alpha Chains/immunology [MESH]
  • |Interferon-gamma/immunology [MESH]
  • |Lung/cytology/*immunology [MESH]
  • |Lymphocyte Activation/immunology [MESH]
  • |Mice [MESH]
  • |Mice, Inbred C57BL [MESH]
  • |Mice, Knockout [MESH]
  • |Mucous Membrane/cytology/immunology [MESH]
  • |Orthomyxoviridae Infections/*immunology [MESH]
  • |T-Box Domain Proteins/*biosynthesis [MESH]


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