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10.3390/ijms21186966

http://scihub22266oqcxt.onion/10.3390/ijms21186966
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32971931!7554897!32971931
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suck abstract from ncbi

pmid32971931      Int+J+Mol+Sci 2020 ; 21 (18): ?
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  • IL-21 in Homeostasis of Resident Memory and Exhausted CD8 T Cells during Persistent Infection #MMPMID32971931
  • Ren HM; Lukacher AE
  • Int J Mol Sci 2020[Sep]; 21 (18): ? PMID32971931show ga
  • CD4 T cells guide the development of CD8 T cells into memory by elaborating mitogenic and differentiation factors and by licensing professional antigen-presenting cells. CD4 T cells also act to stave off CD8 T cell dysfunction during repetitive antigen stimulation in persistent infection and cancer by mitigating generation of exhausted T cells (T(EX)). CD4 T cell help is also required for establishing and maintaining tissue-resident memory T cells (T(RM)), the nonrecirculating memory T cell subset parked in nonlymphoid tissues to provide frontline defense against reinvading pathogens. Interleukin (IL)-21 is the signature cytokine secreted by follicular helper CD4 T cells (T(FH)) to drive B cell expansion and differentiation in germinal centers to mount high-affinity, isotype class-switched antibodies. In several infection models, IL-21 has been identified as the CD4 T help needed for formation and survival of T(RM) and T(EX). In this review, we will explore the different memory subsets of CD8 T cells in persistent infections, the metabolic profiles associated with each, and evidence documenting the importance of CD4 T cell-derived IL-21 in regulating CD8 T(RM) and T(EX) development, homeostasis, and function.
  • |*Immunologic Memory[MESH]
  • |Animals[MESH]
  • |B-Lymphocytes/immunology/pathology[MESH]
  • |CD8-Positive T-Lymphocytes/*immunology/pathology[MESH]
  • |Humans[MESH]
  • |Immunoglobulin Class Switching/immunology[MESH]
  • |Infections/*immunology/pathology[MESH]
  • |Interleukin-21[MESH]
  • |Interleukins/*immunology[MESH]


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