Subject(s)
Antigens, CD34/metabolism , Circoviridae Infections/diagnosis , Gyrovirus/isolation & purification , Hematopoietic Stem Cells/virology , Lymphoma/virology , Umbilical Cord/cytology , Adult , Aged , Child , Circoviridae Infections/virology , DNA, Viral/analysis , Female , Gyrovirus/genetics , Hematopoietic Stem Cells/cytology , Humans , Male , Middle Aged , Polymerase Chain Reaction/methods , Young AdultABSTRACT
Immune reconstitution after allogeneic stem cell transplantation protects against opportunistic infections and disease relapse. Identifying the most protective lymphocyte subset would have implications of adoptive immunotherapy. We followed up a case series of 34 allogeneic transplantations for pediatric leukemias, aplastic anemias, or solid tumors. Regardless of baseline hematologic disorder, the speed of reconstitution of cytotoxic CD8 T lymphocytes and the achieving of the 10th percentile of normal CD4 T lymphocytes (but not B lymphocytes or natural killer cells) conditioned overall survival. The source of hematopoietic stem cells (peripheral blood vs bone marrow) and the occurrence of graft-versus-host disease (either acute or chronic) did not impact on immune reconstitution. Larger case series are needed to confirm the pivotal role of cytotoxic CD8 T lymphocytes in overall survival.
