Neonatal and adult recent thymic emigrants produce IL-8 and express complement receptors CR1 and CR2

نویسندگان

  • Marcin L. Pekalski
  • Arcadio Rubio García
  • Ricardo C. Ferreira
  • Daniel B. Rainbow
  • Deborah J. Smyth
  • Meghavi Mashar
  • Jane Brady
  • Natalia Savinykh
  • Xaquin Castro Dopico
  • Sumiyya Mahmood
  • Simon Duley
  • Helen E. Stevens
  • Neil M. Walker
  • Antony J. Cutler
  • Frank Waldron-Lynch
  • David B. Dunger
  • Claire Shannon-Lowe
  • Alasdair J. Coles
  • Joanne L. Jones
  • Chris Wallace
  • John A. Todd
  • Linda S. Wicker
چکیده

The maintenance of peripheral naive T lymphocytes in humans is dependent on their homeostatic division, not continuing emigration from the thymus, which undergoes involution with age. However, postthymic maintenance of naive T cells is still poorly understood. Previously we reported that recent thymic emigrants (RTEs) are contained in CD31+CD25- naive T cells as defined by their levels of signal joint T cell receptor rearrangement excision circles (sjTRECs). Here, by differential gene expression analysis followed by protein expression and functional studies, we define that the naive T cells having divided the least since thymic emigration express complement receptors (CR1 and CR2) known to bind complement C3b- and C3d-decorated microbial products and, following activation, produce IL-8 (CXCL8), a major chemoattractant for neutrophils in bacterial defense. We also observed an IL-8-producing memory T cell subpopulation coexpressing CR1 and CR2 and with a gene expression signature resembling that of RTEs. The functions of CR1 and CR2 on T cells remain to be determined, but we note that CR2 is the receptor for Epstein-Barr virus, which is a cause of T cell lymphomas and a candidate environmental factor in autoimmune disease.

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عنوان ژورنال:

دوره 2  شماره 

صفحات  -

تاریخ انتشار 2017