Human CD8+ CD57- TEMRA cells: Too young to be called "old"

Kriti Verma, Justyna Ogonek, Pavankumar Reddy Varanasi, Susanne Luther, Ivonne Bünting, Katrin Thomay, Yvonne Lisa Behrens, Eva Mischak-Weissinger, Lothar Hambach

Research output: Contribution to journalArticlepeer-review

20 Citations (Scopus)

Abstract

End-stage differentiation of antigen-specific T-cells may precede loss of immune responses against e.g. viral infections after allogeneic stem cell transplantation (SCT). Antigen-specific CD8+ T-cells detected by HLA/peptide multimers largely comprise CD45RA-/CCR7- effector memory (TEM) and CD45RA+/CCR7- TEMRA subsets. A majority of terminally differentiated T-cells is considered to be part of the heterogeneous TEMRA subset. The senescence marker CD57 has been functionally described in memory T-cells mainly composed of central memory (TCM) and TEM cells. However, its role specifically in TEMRA cells remained undefined. Here, we investigated the relevance of CD57 to separate human CD8+ TEMRA cells into functionally distinct subsets. CD57- CD8+ TEMRA cells isolated from healthy donors had considerably longer telomeres and showed significantly more BrdU uptake and IFN-γ release upon stimulation compared to the CD57+ counterpart. Cytomegalovirus (CMV) specific T-cells isolated from patients after allogeneic SCT were purified into CD57+ and CD57- TEMRA subsets. CMV specific CD57- TEMRA cells had longer telomeres and a considerably higher CMV peptide sensitivity in BrdU uptake and IFN-γ release assays compared to CD57+ TEMRA cells. In contrast, CD57+ and CD57- TEMRA cells showed comparable peptide specific cytotoxicity. Finally, CD57- CD8+ TEMRA cells partially changed phenotypically into TEM cells and gained CD57 expression, while CD57+ CD8+ TEMRA cells hardly changed phenotypically and showed considerable cell death after in vitro stimulation. To the best of our knowledge, these data show for the first time that CD57 separates CD8+ TEMRA cells into a terminally differentiated CD57+ population and a so far functionally undescribed "young" CD57- TEMRA subset with high proliferative capacity and differentiation plasticity.

Original languageEnglish
Article numbere0177405
JournalPLoS ONE
Volume12
Issue number5
DOIs
Publication statusPublished - 8 May 2017

Keywords

  • CD57 Antigens/immunology
  • CD8-Positive T-Lymphocytes/immunology
  • Cell Proliferation
  • Cells, Cultured
  • Humans
  • Immunologic Memory
  • T-Lymphocyte Subsets

Fingerprint

Dive into the research topics of 'Human CD8+ CD57- TEMRA cells: Too young to be called "old"'. Together they form a unique fingerprint.

Cite this