Abstract
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.
Original language | English |
---|---|
Pages (from-to) | 1774-1779 |
Number of pages | 6 |
Journal | Transplantation |
Volume | 78 |
Issue number | 12 |
DOIs | |
Publication status | Published - 27 Dec 2004 |
Keywords
- Adoptive T-cell transfer
- aHLI
- GvHD
- Immunology
- Liver transplantation