Clinical characteristics of 114 patients who received EBV-specific CTLs after transplantation
Characteristic . | CTL recipients . |
---|---|
Age at transplantation, y [mean (range)] | 8.4 (0.5-38) |
Male:female | 69:45 |
Diagnosis | |
Acute lymphoblastic leukemia | 29 |
Acute myeloid leukemia | 33 |
Myelodysplasia | 11 |
Acute undifferentiated leukemia | 1 |
Chronic myeloid leukemia | 12 |
Hodgkin disease | 1 |
Non-Hodgkin lymphoma | 3 |
Aplastic anemia | 1 |
Paroxysmal nocturnal hemoglobinuria | 2 |
Histiocytic disorders | 3 |
Hurler syndrome | 2 |
X-linked lymphoproliferative disease | 6 |
Wiskott-Aldrich syndrome | 5 |
Osteogenesis imperfecta | 3 |
Common immunodeficiency | 2 |
Type of transplantation | |
Unrelated donor | |
10/10 match | 3 |
9/10 match | 4 |
6/6 match | 63 |
5/6 match | 30 |
Family member | |
Syngeneic | 1 |
5/6 match | 6 |
4/6 match | 4 |
3/6 match | 3 |
HSC product | |
Marrow | 108 |
PBSC | 6 |
Characteristic . | CTL recipients . |
---|---|
Age at transplantation, y [mean (range)] | 8.4 (0.5-38) |
Male:female | 69:45 |
Diagnosis | |
Acute lymphoblastic leukemia | 29 |
Acute myeloid leukemia | 33 |
Myelodysplasia | 11 |
Acute undifferentiated leukemia | 1 |
Chronic myeloid leukemia | 12 |
Hodgkin disease | 1 |
Non-Hodgkin lymphoma | 3 |
Aplastic anemia | 1 |
Paroxysmal nocturnal hemoglobinuria | 2 |
Histiocytic disorders | 3 |
Hurler syndrome | 2 |
X-linked lymphoproliferative disease | 6 |
Wiskott-Aldrich syndrome | 5 |
Osteogenesis imperfecta | 3 |
Common immunodeficiency | 2 |
Type of transplantation | |
Unrelated donor | |
10/10 match | 3 |
9/10 match | 4 |
6/6 match | 63 |
5/6 match | 30 |
Family member | |
Syngeneic | 1 |
5/6 match | 6 |
4/6 match | 4 |
3/6 match | 3 |
HSC product | |
Marrow | 108 |
PBSC | 6 |
EBV indicates Epstein-Barr virus; CTL, cytotoxic T lymphocyte; HSC, hematopoietic stem cell; and PBSC, peripheral blood stem cell.