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Volume 12, Issue 12, Pages 1335-1342 (December 2006)


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Antigen-Specific T-Lymphocyte Function After Cord Blood Transplantation

Geoff Cohen1, Shelly L. Carter1, Kenneth I. Weinberg2, Bernadette Masinsin2, Eva Guinan3, Joanne Kurtzberg4, John E. Wagner6, Nancy A. Kernan7, Robertson Parkman2Corresponding Author Informationemail address

Received 21 June 2006; accepted 18 August 2006.

Abstract 

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 1 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.

1 The EMMES Corporation, Rockville, Maryland

2 Department of Pediatrics, Childrens Hospital Los Angeles, Los Angeles, California

3 Pediatric Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts

4 Department of Pediatrics, Duke University Medical Center, Durham, North Carolina

6 Department of Pediatrics, University of Minnesota, Minneapolis, Minnesota

7 Department of Pediatrics, Memorial Sloan-Kettering Cancer Center, New York, New York

Corresponding Author InformationCorrespondence and reprint requests: Robertson Parkman, MD, Division of Research Immunology/Bone Marrow Transplantation, Childrens Hospital Los Angeles, The Saban Research Institute, 4650 Sunset Boulevard, Mail Stop 62, Los Angeles, CA 90027.

PII: S1083-8791(06)00578-7

doi:10.1016/j.bbmt.2006.08.036


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