Direct visualization of cytomegalovirus-specific T-cell reconstitution after allogeneic stem cell transplantation

Cytomegalovirus (CMV) remains an important cause of morbidity and mortality after allogeneic stem cell transplantation (SCT), but cytotoxic T lymphocytes (CTL) may play a critical role in controlling CMV reactivation. Fluorescent HLA-peptide tetramers containing immunodominant peptides from CMV were...

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Veröffentlicht in:Blood 2001-03, Vol.97 (5), p.1232-1240
Hauptverfasser: Cwynarski, Kate, Ainsworth, Jenni, Cobbold, Mark, Wagner, Simon, Mahendra, Prem, Apperley, Jane, Goldman, John, Craddock, Charles, Moss, Paul A.H.
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container_end_page 1240
container_issue 5
container_start_page 1232
container_title Blood
container_volume 97
creator Cwynarski, Kate
Ainsworth, Jenni
Cobbold, Mark
Wagner, Simon
Mahendra, Prem
Apperley, Jane
Goldman, John
Craddock, Charles
Moss, Paul A.H.
description Cytomegalovirus (CMV) remains an important cause of morbidity and mortality after allogeneic stem cell transplantation (SCT), but cytotoxic T lymphocytes (CTL) may play a critical role in controlling CMV reactivation. Fluorescent HLA-peptide tetramers containing immunodominant peptides from CMV were used to prospectively monitor the recovery of CMV CTL in recipients of allogeneic transplants from siblings (n = 13) or unrelated donors (n = 11). In patients given allografts from a sibling when both the patient and donor were seropositive for CMV before SCT, recovery of CMV-specific CTL was rapid and reached up to 21% of all CD8+ T cells. Early reconstitution of CMV-specific immunity was not observed if either the donor or recipient was seronegative for CMV. In recipients of transplants from volunteer unrelated donors, recovery of CMV-specific CTL was delayed in comparison to that in recipients of transplants from siblings and no CTL were observed within the first 100 days after SCT. CTL numbers were increased after episodes of CMV reactivation but were suppressed by prednisolone therapy. Recovery of CMV-specific CTL to levels greater than 10 × 106/L was associated with protection from CMV disease. It was concluded that use of HLA-peptide tetramers to quantify CMV CTL is valuable for studying T-cell responses after allogeneic SCT. It should allow prediction of CMV reactivation in individual patients and assist in the development of adoptive T-cell immunotherapy.
doi_str_mv 10.1182/blood.V97.5.1232
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Fluorescent HLA-peptide tetramers containing immunodominant peptides from CMV were used to prospectively monitor the recovery of CMV CTL in recipients of allogeneic transplants from siblings (n = 13) or unrelated donors (n = 11). In patients given allografts from a sibling when both the patient and donor were seropositive for CMV before SCT, recovery of CMV-specific CTL was rapid and reached up to 21% of all CD8+ T cells. Early reconstitution of CMV-specific immunity was not observed if either the donor or recipient was seronegative for CMV. In recipients of transplants from volunteer unrelated donors, recovery of CMV-specific CTL was delayed in comparison to that in recipients of transplants from siblings and no CTL were observed within the first 100 days after SCT. CTL numbers were increased after episodes of CMV reactivation but were suppressed by prednisolone therapy. Recovery of CMV-specific CTL to levels greater than 10 × 106/L was associated with protection from CMV disease. 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subjects Adolescent
Adult
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Anti-Inflammatory Agents - administration & dosage
Antigens, Viral - blood
Biological and medical sciences
Bone marrow, stem cells transplantation. Graft versus host reaction
Cohort Studies
Cytomegalovirus - drug effects
Cytomegalovirus - growth & development
Cytomegalovirus - immunology
Cytomegalovirus Infections - drug therapy
Cytomegalovirus Infections - etiology
Female
Hematopoietic Stem Cell Transplantation - adverse effects
Humans
Lymphocyte Count
Male
Medical sciences
Middle Aged
Molecular Probes
Phosphoproteins - blood
Prednisolone - administration & dosage
Prospective Studies
T-Lymphocytes, Cytotoxic - cytology
T-Lymphocytes, Cytotoxic - immunology
T-Lymphocytes, Cytotoxic - virology
Time Factors
Transfusions. Complications. Transfusion reactions. Cell and gene therapy
Transplantation, Homologous - adverse effects
Viral Matrix Proteins - blood
Virus Activation - immunology
title Direct visualization of cytomegalovirus-specific T-cell reconstitution after allogeneic stem cell transplantation
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