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Updated: Jul 18, 2026

Expanding Cytotoxic T Lymphocytes from Umbilical Cord Blood that Target Cytomegalovirus, Epstein-Barr Virus, and Adenovirus
Published on: May 7, 2012
Antigen-specific T-lymphocyte function after cord blood transplantation
Geoff Cohen1, Shelly L Carter, Kenneth I Weinberg
1The EMMES Corporation, Rockville, Maryland, USA.
Naive T lymphocytes in hematopoietic stem cell (HSC) products can generate antigen-specific immunity post-transplant. This study in unrelated cord blood transplantation (UCBT) shows early herpesvirus-specific T cell immunity development.
Area of Science:
- Immunology
- Transplantation Science
- Virology
Background:
- Determining naive T cell contribution to immunity post-hematopoietic stem cell transplantation (HSCT) is challenging due to donor T cells.
- Umbilical cord blood (UCB) offers a unique source of naive T lymphocytes for transplantation.
Purpose of the Study:
- To evaluate the role of naive T lymphocytes in early antigen-specific immune reconstitution after unrelated cord blood transplantation (UCBT).
- To assess the development of T lymphocytes specific for herpesviruses following UCBT.
Main Methods:
- Longitudinal evaluation of UCBT recipients for herpesvirus-specific T lymphocytes.
- Analysis of T cell reconstitution, transplant factors, and graft-versus-host disease (GVHD).
Main Results:
- Antigen-specific T lymphocytes were detected early after UCBT (HSV day 29, CMV day 44, VZV day 94).
- 66 out of 153 UCBT recipients developed T cell responses to at least one herpesvirus.
- Response development was independent of T cell reconstitution, cell dose, disease, or GVHD.
Conclusions:
- Naive T lymphocytes within the hematopoietic stem cell inoculum can initiate antigen-specific T cell immunity early post-transplant.
- UCBT recipients can mount early T cell responses to common viral antigens, highlighting the functional capacity of naive T cells.
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