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Prepublished online as a Blood First Edition Paper on March 20, 2003; DOI 10.1182/blood-2002-10-3170.

Submitted October 21, 2002
Accepted March 4, 2003
Multiparity induces priming to male-specific minor histocompatibility antigen, HY, in mice and humans
Edward James, Jian-Guo Chai, Hamlata Dewchand, Eugenio Macchiarulo, Francesco Dazzi, and Elizabeth Simpson*
Transplantation Biology Group, Clinical Sciences Centre, Imperial College Faculty of Medicine, London, United Kingdom
Department of Immunology, Imperial College Faculty of Medicine, London, United Kingdom
* Corresponding author; email: esimpson{at}ic.ac.uk.
One of the factors which increases the risk of graft-versus-host disease following allogeneic stem cell transplantation is the use of multiparous females as donors. Since minor histocompatibility (H) antigens are the main targets of graft-versus-host and graft-versus-leukemia responses, we tested the hypothesis that multiparity could prime minor H antigen-specific T cells. We examined the peripheral lymphoid populations of multiparous mice and humans for evidence of priming of CD8+ T cytotoxic lymphocytes against peptide epitopes of the male-specific minor H antigen, HY. In contrast to naive females, multiparous females have measurable levels of circulating HY-specific tetramer-positive T lymphocytes, which can be readily expanded in vitro. These findings have implications for the in vitro generation of T cell clones as reagents for immunotherapy for tumours following stem cell transplantation.

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