4.8 Article

CD49a Expression Defines Tissue-Resident CD8+ T Cells Poised for Cytotoxic Function in Human Skin

期刊

IMMUNITY
卷 46, 期 2, 页码 287-300

出版社

CELL PRESS
DOI: 10.1016/j.immuni.2017.01.009

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资金

  1. Novartis
  2. Swedish Research Council
  3. Ragnar Soderberg Stiftelse
  4. Svenska Lakaresallskapet
  5. Stockholm County Council
  6. Psoriasisfonden
  7. Hudfonden
  8. European Research Council under the European Union [311335]
  9. Swedish Cancer Foundation
  10. Swedish Foundation for Strategic Research
  11. Stockholm City Council
  12. Karolinska Institutet Center for Innovative Medicine
  13. Wallenberg Foundation
  14. European Research Council (ERC) [311335] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

Tissue-resident memory T (Trm) cells form a heterogeneous population that provides localized protection against pathogens. Here, we identify CD49a as a marker that differentiates CD8(+) Trm cells on a compartmental and functional basis. In human skin epithelia, CD8(+)CD49a(+) Trm cells produced interferon-g, whereas CD8(+)CD49a(-) Trm cells produced interleukin-17 (IL-17). In addition, CD8(+)CD49a(+) Trm cells from healthy skin rapidly induced the expression of the effector molecules perforin and granzyme B when stimulated with IL-15, thereby promoting a strong cytotoxic response. In skin from patients with vitiligo, where melanocytes are eradicated locally, CD8(+)CD49a(+) Trm cells that constitutively expressed perforin and granzyme B accumulated both in the epidermis and dermis. Conversely, CD8(+)CD49a(-) Trm cells from psoriasis lesions predominantly generated IL-17 responses that promote local inflammation in this skin disease. Overall, CD49a expression delineates CD8(+) Trm cell specialization in human epithelial barriers and correlates with the effector cell balance found in distinct inflammatory skin diseases.

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