Author/Authors :
Maria De Ioanni، نويسنده , , Mauro Di Ianni، نويسنده , , Elisabetta Bonifacio، نويسنده , , Lorenzo Moretti، نويسنده , , Debora Cecchini، نويسنده , , Federico Bazzucchi، نويسنده , , Adelmo Terenzi، نويسنده , , Teresa Aloisi، نويسنده , , Franca Falzetti، نويسنده , , Franco Aversa، نويسنده , , Yair Reisner، نويسنده , , Massimo F. Martelli، نويسنده , , Antonio Tabilio، نويسنده ,
Abstract :
Although adoptive transfer of donor lymphocytes protects from infections and relapse after allogeneic hematopoietic stem cell transplantation in both mice and in men, it is associated with a high risk of graft versus host disease (GvHD) which rises with HLA mismatching and the number of T lymphocytes that are infused. Elimination/reduction of alloreactive donor T lymphocytes is an appealing approach and several strategies have been proposed. Here we describe generation of anti-3rd party T lymphocytes under conditions of IL-2 deprivation and their effects in a pre-clinical murine model.
Our results clearly indicated that anti-3rd party T lymphocytes generated on a large scale by means of IL-2 deprivation maintain a broad T cell repertoire, do not proliferate in a mixed lymphocyte reaction and do not cause GvHD in NOD–SCID mice. These anti-3rd party lymphocytes contain a large adaptive T regulatory cell subset which might contribute to in vitro and in vivo immune modulation.