Dj. Diamond et al., IMMUNOHISTOCHEMICAL ANALYSIS OF T-CELL PHENOTYPES IN PATIENTS WITH GRAFT-VERSUS-HOST DISEASE FOLLOWING ALLOGENEIC BONE-MARROW TRANSPLANTATION, Transplantation, 59(10), 1995, pp. 1436-1444
Allogeneic bone marrow transplantation has become the therapy of choic
e in many cases of hematologic malignancy. In both matched related don
or transplants-and, to a greater degree, in unrelated donor transplant
situations-a major complication of the procedure is GVHD. This proble
m is caused by mature T cells in the graft, which also facilitate engr
aftment, and mediate an antitumor effect to reduce relapse. In order t
o further characterize the T cells that are present at the GVHD site o
f injury, we have studied 134 fresh tissue biopsies using immunohistoc
hemical methods from 50 consecutive ABMT recipients clinically suspect
ed of having acute GVHD. Antibodies specific for T cells, T cell recep
tor subsets, B cells, and NK cells were used to characterize the lymph
ocytic infiltrate in the biopsy tissue from GVHD patients. The data sh
owed that the majority of lymphocytes that had infiltrated the epithel
ium or epidermis were CD3+ T cells. Using antibodies that distinguishe
d the alpha/beta (beta F1) from the gamma/delta TCR (TCR delta 1)-expr
essing T cells, we observed that the lymphocytic infiltrates from invo
lved tissues of the gastrointestinal tract, skin, and liver are almost
exclusively derived from the alpha/beta expressing T cell subset, and
are of the memory cell subset of T cells (CD45RO). This is in contras
t to some examples from other disease states, in which a significant p
roportion of the lymphocytes that infiltrate the epidermal layers are
of the gamma/delta type.