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Skin and heart allograft rejection solely by long-lived alloreactive T(RM) cells in skin of severe combined immunodeficient mice
Whether induced tissue-resident memory T (T(RM)) cells in nonlymphoid organs alone can mediate allograft rejection is unknown. By grafting alloskin or heart into severe combined immunodeficient or Rag2KO mice in which a piece of induced CD4(+) and/or CD8(+) T(RM) cell–containing MHC-matched or synge...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8791614/ https://www.ncbi.nlm.nih.gov/pubmed/35080985 http://dx.doi.org/10.1126/sciadv.abk0270 |
Sumario: | Whether induced tissue-resident memory T (T(RM)) cells in nonlymphoid organs alone can mediate allograft rejection is unknown. By grafting alloskin or heart into severe combined immunodeficient or Rag2KO mice in which a piece of induced CD4(+) and/or CD8(+) T(RM) cell–containing MHC-matched or syngeneic skin was transplanted in advance, we addressed this issue. The induced CD4(+) T(RM) cells in the skin alone acutely rejected alloskin or heart grafts. RNA-seq analysis showed that induced CD4(+) T(RM) cells in skin favorably differentiated into T(H)17-like polarization during the secondary immune response. Inhibition of the key T(H)17 signaling molecule RORγt attenuated T(RM) cell–mediated graft rejection. Thus, we offer a unique mouse model to specifically study T(RM) cell–mediated allograft rejection without the involvement of lymphocytes in lymphoid organs and tissues. Our study provides strong evidence supporting the hypothesis that long-lived alloreactive T(RM) cells resident in other organs/tissues substantially contribute to organ allograft rejection. |
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