Maintenance of CD8+ memory T lymphocytes in the spleen but not in the bone marrow is dependent on proliferation

نویسندگان

  • Francesco Siracusa
  • Özen Sercan Alp
  • Patrick Maschmeyer
  • Mairi McGrath
  • Mir-Farzin Mashreghi
  • Shintaro Hojyo
  • Hyun-Dong Chang
  • Koji Tokoyoda
  • Andreas Radbruch
چکیده

It is current belief that numbers of CD8+ memory T lymphocytes in the memory phase of an immune response are maintained by homeostatic proliferation. Here, we compare the proliferation of CD8+ memory T lymphocytes, generated by natural infections and by intentional immunization, in spleen and bone marrow (BM). Fifty percent of CD8+ memory T lymphocytes in the spleen are eliminated by cyclophosphamide within 14 days, indicating that numbers of at least 50% of splenic CD8+ memory T lymphocytes are maintained by proliferation. The numbers of CD8+ memory T lymphocytes in the BM, however, were not affected by cyclophosphamide. This stability was independent of circulating CD8+ memory T cells, blocked by FTY720, showing that BM is a privileged site for the maintenance of memory T lymphocytes, as resident cells, resting in terms of proliferation.

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عنوان ژورنال:

دوره 47  شماره 

صفحات  -

تاریخ انتشار 2017