[HTML][HTML] Clonable T lymphocytes in T cell-depleted bone marrow transplants correlate with development of graft-v-host disease

NA Kernan, NH Collins, L Juliano, T Cartagena… - Blood, 1986 - Elsevier
NA Kernan, NH Collins, L Juliano, T Cartagena, B Dupont, RJ O'Reilly
Blood, 1986Elsevier
Early clinical trials using T lymphocyte-depleted human marrow for transplantation have
reported that such grafts reduce, to varying degrees, both the incidence and the severity of
graft-v-host disease (GVHD). However, to date, no clear estimates have been made as to
what degree of T cell depletion is necessary to prevent GVHD in every case. To address this
problem, we used a limiting dilution assay (LDA) to quantitate residual clonable T
lymphocytes in human T cell-depleted bone marrow in 31 HLA-identical transplants for …
Early clinical trials using T lymphocyte-depleted human marrow for transplantation have reported that such grafts reduce, to varying degrees, both the incidence and the severity of graft-v-host disease (GVHD). However, to date, no clear estimates have been made as to what degree of T cell depletion is necessary to prevent GVHD in every case. To address this problem, we used a limiting dilution assay (LDA) to quantitate residual clonable T lymphocytes in human T cell-depleted bone marrow in 31 HLA-identical transplants for leukemia. The number of phytohemagglutinin -interleukin 2-responsive T lymphocytes determined by LDA and expressed as T cell per kilogram recipient weight was found to correlate with the subsequent development of GVHD: no patients who received less than 1 × 106 T cell per kilogram developed GVHD (N = 24). Of the seven patients who received 1 × 105 to 4.4 × 105 T cell per kilogram, four patients developed grade I or II skin GVHD. This study thus provides a quantitative estimate of the number of T lymphocytes necessary to initiate clinically detectable GVHD in an HLA-identical host.
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