Immune monitoring with iTAg MHC Tetramers for prediction of recurrent or persistent cytomegalovirus infection or disease in allogeneic hematopoietic stem cell transplant recipients: a prospective multicenter study

Author:

Gratama Jan W.1,Boeckh Michael2,Nakamura Ryotaro3,Cornelissen Jan J.4,Brooimans Rik A.1,Zaia John A.5,Forman Stephen J.3,Gaal Karl6,Bray Kurtis R.7,Gasior Gail H.7,Boyce Christopher S.7,Sullivan Linda A.7,Southwick Paula C.7

Affiliation:

1. Department of Clinical and Tumor Immunology, Erasmus Medical Center/Daniel den Hoed Cancer Center, Rotterdam, The Netherlands;

2. Program in Infectious Diseases, Fred Hutchinson Cancer Research Center, Seattle, WA;

3. Division of Hematology and Hematopoietic Cell Transplantation, City of Hope National Medical Center, Duarte, CA;

4. Department of Hematology, Erasmus Medical Center/Daniel den Hoed Cancer Center, Rotterdam, The Netherlands;

5. Department of Virology, City of Hope National Medical Center, Duarte, CA;

6. Division of Pathology, City of Hope National Medical Center, Duarte, CA; and

7. Department of Clinical Research, Beckman Coulter, Carlsbad, CA

Abstract

Abstract Cytomegalovirus (CMV) infection is an important cause of morbidity and mortality in hematopoietic stem cell transplant recipients despite the introduction of posttransplantation viral monitoring and preemptive antiviral therapy. We evaluated the use of HLA class I tetramers in monitoring CMV-specific T-cell recovery to predict patients at risk for CMV-related complications. This prospective multicenter clinical trial obtained nearly 1400 tetramer/allele results in more than 800 biweekly blood samples from 83 patients monitored for 1 year after transplantation. Major HLA types were included (A*0101, A*0201, B*0702, B*0801, B*3501). iTAg MHC Tetramers (Beckman Coulter) were used to enumerate CMV-specific CD8+ T cells by flow cytometry using a single-platform absolute counting method. Assay variability was 8% or less and results were available within 3 hours. Delayed recovery of CMV-specific T cells (< 7 cells/μL in all blood samples during the first 65 days after transplantation) was found to be a significant risk factor for CMV-related complications; these patients were more likely to develop recurrent or persistent CMV infection (relative risk 2.6, CI 1.2-5.8, P = .01) than patients showing rapid recovery, which was associated with protection from CMV-related complications (P = .004). CMV tetramer–based immune monitoring, in conjunction with virologic monitoring, can be an important new tool to assess risk of CMV-related complications and to guide preemptive therapeutic choices.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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