Control of organ transplant-associated graft-versus-host disease by activated host lymphocyte infusions

被引:40
作者
Kuball, J
Theobald, M
Ferreira, EA
Hess, G
Burg, J
Maccagno, G
Barreiros, AP
Lüth, S
Schimanski, CC
Schuchmann, M
Schwarting, A
Neurath, M
Otto, G
Galle, PR
Lohse, AW
机构
[1] Johannes Gutenberg Univ Mainz, Dept Hematol & Oncol, D-55101 Mainz, Germany
[2] Johannes Gutenberg Univ Mainz, Inst Pathol, D-55101 Mainz, Germany
[3] Johannes Gutenberg Univ Mainz, Transfus Ctr, D-55101 Mainz, Germany
[4] Johannes Gutenberg Univ Mainz, Dept Internal Med 1, D-55101 Mainz, Germany
[5] Johannes Gutenberg Univ Mainz, Dept Transplantat & Hepatobiliary Surg, D-55101 Mainz, Germany
关键词
liver transplantation; immunology; GvHD; adoptive T-cell transfer; aHLI;
D O I
10.1097/01.TP.0000144183.77279.EC
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Prolonged persistence of donor-derived T cells after organ transplantation has been proposed to improve long-term allograft survival. However, surviving transplant-derived T cells are also able to mediate devastating graft-versus-host disease (GvHD). Currently, GvHD after organ transplantation is usually refractory to conventional therapy and the disease outcome fatal. Methods. Graft-reactive host T cells were generated ex vivo from a patient suffering from a severe and refractory liver-transplant-associated GvHD. To control GvHD, activated alloreactive host T cells were repetitively retransferred into the patient (activated host lymphocyte infusion [aHLI]). Results. Adoptive transfer of ex vivo activated alloreactive host T cells (aHLI) led to the control and complete resolution of severe GvHD without inducing allograft rejection. Conclusions. aHLI opens a novel therapeutic window to control solid-organ transplant-associated GvHD while preserving allograft integrity.
引用
收藏
页码:1774 / 1779
页数:6
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