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CD69+ memory T lymphocytes of the bone marrow and spleen express the signature transcripts of tissue-resident memory T lymphocytes.

Francesco SiracusaPawel DurekMairi A McGrathÖzen Sercan-AlpAnna RaoWeijie DuCarla CendónHyun-Dong ChangGitta Anne HeinzMir-Farzin MashreghiAndreas RadbruchJun Dong
Published in: European journal of immunology (2019)
It is a matter of current debate whether the bone marrow is a hub for circulating memory T lymphocytes and/or the home of resident memory T lymphocytes. Here we demonstrate for CD69+ murine CD8+ , and CD69+ murine and human CD4+ memory T lymphocytes of the bone marrow, making up between 30 and 60% of bone marrow memory T lymphocytes, that they express the gene expression signature of tissue-resident memory T lymphocytes. This suggests that a substantial proportion of bone marrow memory T lymphocytes are resident. It adds to previous evidence that bone marrow memory T cells are resting in terms of mobility and proliferation, and maintain exclusive long-term memory to distinct, systemic antigens.
Keyphrases
  • bone marrow
  • working memory
  • mesenchymal stem cells
  • gene expression
  • patient safety
  • healthcare
  • signaling pathway
  • quality improvement
  • dna methylation
  • blood pressure
  • immune response
  • dendritic cells
  • emergency medicine