Literature DB >> 15997467

Amelioration of acute graft-versus-host disease by NKG2A engagement on donor T cells.

Hiroki Kawamura1, Hideo Yagita, Tetsuro Nisizawa, Nakako Izumi, Chikako Miyaji, Russell E Vance, David H Raulet, Ko Okumura, Toru Abo.   

Abstract

Acute graft-versus-host disease (aGVHD) remains a major complication of allogeneic bone marrow transplantation, which is caused by donor T cells specific for host alloantigens. In a murine model, we found that donor T cells expressed a natural killer cell inhibitory receptor, CD94/NKG2A, during the course of aGVHD. Administration of an anti-NKG2A mAb markedly inhibited the expansion of donor T cells and ameliorated the aGVHD pathologies. These results suggested that the CD94/NKG2A inhibitory receptor expressed on host-reactive donor T cells can be a novel target for the amelioration of aGVHD.

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Year:  2005        PMID: 15997467     DOI: 10.1002/eji.200425933

Source DB:  PubMed          Journal:  Eur J Immunol        ISSN: 0014-2980            Impact factor:   5.532


  3 in total

1.  NKG2A and CD56 are coexpressed on activated TH2 but not TH1 lymphocytes.

Authors:  Robert J Freishtat; Lindsay W Mitchell; Svetlana D Ghimbovschi; Samuel B Meyers; Eric P Hoffman
Journal:  Hum Immunol       Date:  2006-03-27       Impact factor: 2.850

2.  T-bet is critical for the development of acute graft-versus-host disease through controlling T cell differentiation and function.

Authors:  Jianing Fu; Dapeng Wang; Yu Yu; Jessica Heinrichs; Yongxia Wu; Steven Schutt; Kane Kaosaard; Chen Liu; Kelley Haarberg; David Bastian; Daniel G McDonald; Claudio Anasetti; Xue-Zhong Yu
Journal:  J Immunol       Date:  2014-11-17       Impact factor: 5.422

3.  NKG2A inhibits TH2 cell effector function in vitro.

Authors:  Robert J Freishtat; Bahar Mojgani; Maryam Nazemzadeh; Kanneboyina Nagaraju; Eric P Hoffman
Journal:  BMC Pulm Med       Date:  2007-10-10       Impact factor: 3.317

  3 in total

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