4.2 Article

Antigen-specific T-lymphocyte function after cord blood transplantation

Journal

BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION
Volume 12, Issue 12, Pages 1335-1342

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.bbmt.2006.08.036

Keywords

immune reconstitution; antigen-specific immune function; cord blood transplantation

Funding

  1. NCI NIH HHS [P01-CA100265, P01 CA100265] Funding Source: Medline
  2. NHLBI NIH HHS [N01HB67138, N01-HB-67135, N01HB67135, N01-HB-67113, N01-HB-67139, N01-HB-67138, N01HB67132, N01-HB-67132, N01HB67139] Funding Source: Medline

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It has not been possible to determine the singular contribution of naive T lymphocytes to antigen-specific immunity after hematopoietic stem cell transplantation (HSCT), because of the confounding effects of donor-derived antigen-specific T lymphocytes present in most hematopoietic stem cell (HSC) products. Because umbilical cord blood contains only naive T lymphocytes, we longitudinally evaluated the recipients of unrelated cord blood transplantation (UCBT) for the presence of T lymphocytes with specificity for herpesviruses, to determine the contribution of the naive T lymphocytes to antigen-specific immune reconstitution after HSCT. Antigen-specific T lymphocytes were detected early after UCBT (herpes simplex virus on day 29; cytomegalovirus on day 44; varicella zoster virus on day 94). Overall, 66 of 153 UCBT recipients developed antigen-specific T lymphocytes to I or more herpesviruses during the evaluation period. The likelihood of developing antigen-specific T lymphocyte function was not associated with immunophenotypic T lymphocyte reconstitution, transplant cell dose, primary disease, or acute and chronic graft-versus-host disease. These results indicate that naive T lymphocytes present in the HSC inoculum can contribute to the generation of antigen-specific T-lymphocyte immunity early after transplantation. (C) 2006 American Society fir Blood and Marrow Transplantation.

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