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Prepublished online as a Blood First Edition Paper on July 12, 2002; DOI 10.1182/blood-2002-02-0657.

Submitted February 28, 2002
Accepted July 2, 2002
Lack of proliferative capacity of human effector and memory T cells expressing killer cell lectin-like receptor G1 (KLRG1)
David Voehringer, Marie Koschella, and Hanspeter Pircher*
Immunology, Institute for Medical Microbiology and Hygiene, University of Freiburg, Freiburg, Germany
* Corresponding author; email: pircher{at}UKL.uni-freiburg.de.
Adaptive immunity necessitates proliferation of lymphocytes. In the mouse, we have previously shown that antigen-experienced T cells that have lost their proliferative potential express the killer cell lectin-like receptor G1 (KLRG1). By using a newly generated monoclonal antibody specific for human KLRG1, we now demonstrate that expression of KLRG1 also identifies T cells in humans which are capable of secreting cytokines but fail to proliferate after stimulation. Furthermore, our data show that proliferative incapacity of CD8 T cells correlates better with KLRG1 expression than with absence of the CD28 marker. In peripheral blood lymphocytes (PBL) from healthy adult donors, KLRG1 was expressed on 44±14 % of CD8 and 18±10 % of CD4 T cells. KLRG1 expression was restricted to antigen-experienced T cells and here, KLRG1+ cells were preferentially found in the CCR7- effector T cell pool. Beside T cells, a significant portion (~ 50%) of human NK cells expressed KLRG1. Interestingly, these KLRG1+ NK cells were found exclusively in the CD56dim NK cell subset. Thus, expression of KLRG1 identifies a subset of NK cells and antigen-experienced T cells in humans which lack proliferative capacity.

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