[HTML][HTML] Ex vivo expansion and prophylactic infusion of CMV-pp65 peptide-specific cytotoxic T-lymphocytes following allogeneic hematopoietic stem cell …

K Micklethwaite, A Hansen, A Foster, E Snape… - Biology of Blood and …, 2007 - Elsevier
K Micklethwaite, A Hansen, A Foster, E Snape, V Antonenas, M Sartor, P Shaw, K Bradstock…
Biology of Blood and Marrow Transplantation, 2007Elsevier
Cytomegalovirus reactivation and infection post-allogeneic hematopoietic stem cell
transplant continue to cause morbidity and mortality. Current pharmacologic therapies are
limited by side effects. Adoptive transfer of ex vivo generated cytomegalovirus-specific T
cells has the potential to restore immunity, prevent cytomegalovirus, and circumvent the
need for pharmacologic therapies. We have generated donor-derived cytomegalovirus-
specific cytotoxic T cells using dendritic cells pulsed with the HLA-A2 restricted nonapeptide …
Cytomegalovirus reactivation and infection post-allogeneic hematopoietic stem cell transplant continue to cause morbidity and mortality. Current pharmacologic therapies are limited by side effects. Adoptive transfer of ex vivo generated cytomegalovirus-specific T cells has the potential to restore immunity, prevent cytomegalovirus, and circumvent the need for pharmacologic therapies. We have generated donor-derived cytomegalovirus-specific cytotoxic T cells using dendritic cells pulsed with the HLA-A2 restricted nonapeptide NLVPMVATV (NLV) derived from the cytomegalovirus-pp65 protein. These cytotoxic T cells have been given prophylactically to 9 recipients aged 4 to 65 years on or after day 28 post-allogeneic hematopoietic stem cell transplant. Only 2 of 9 recipients received T cell depletion in vivo or in vitro. There were no immediate adverse reactions to the infusions. During 97-798 days of follow-up, 2 recipients developed cytomegalovirus reactivation; neither developed cytomegalovirus disease or required pharmacotherapy. Three recipients developed acute graft versus host disease after infusion. Two recipients died, 1 from thrombotic thrombocytopenia purpura secondary to cyclosporine, 1 from complications of graft versus host disease. A transient increase in numbers of cytomegalovirus-specific T cells demonstrated by NLV-tetramer binding was seen in 6 recipients. Prophylactic adoptive transfer of NLV-specific T cells is safe and may be effective in preventing cytomegalovirus reactivation.
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