Antigen-specific T-lymphocyte function after cord blood transplantation

被引:46
作者
Cohen, Geoff
Carter, Shelly L.
Weinberg, Kenneth I.
Masinsin, Bernadette
Guinan, Eva
Kurtzberg, Joanne
Wagner, John E.
Kernan, Nancy A.
Parkman, Robertson
机构
[1] Childrens Hosp Los Angeles, Saban Res Inst, Dept Pediat, Div Res Immunol Bone Marrow Transplantat, Los Angeles, CA 90027 USA
[2] EMMES Corp, Rockville, MD USA
[3] Dana Farber Canc Inst, Boston, MA 02115 USA
[4] Duke Univ, Med Ctr, Dept Pediat, Durham, NC 27710 USA
[5] Univ Minnesota, Dept Pediat, Minneapolis, MN 55455 USA
[6] Mem Sloan Kettering Canc Ctr, Dept Pediat, New York, NY 10021 USA
关键词
immune reconstitution; antigen-specific immune function; cord blood transplantation;
D O I
10.1016/j.bbmt.2006.08.036
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:1335 / 1342
页数:8
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