Effective and long-term control of EBV PTLD after transfer of peptide-selected T cells

Author:

Moosmann Andreas12,Bigalke Iris3,Tischer Johanna4,Schirrmann Leah4,Kasten Julitta3,Tippmer Stefanie3,Leeping Marina4,Prevalšek Dušan4,Jaeger Gundula5,Ledderose Georg4,Mautner Josef6,Hammerschmidt Wolfgang2,Schendel Dolores J.7,Kolb Hans-Jochem4

Affiliation:

1. Clinical Cooperation Group Molecular Oncology, Helmholtz Zentrum München and Ludwig-Maximilians-Universität, Munich;

2. Department of Gene Vectors, Helmholtz Zentrum München, Munich;

3. GMP Group, Institute of Molecular Immunology, Helmholtz Zentrum München, Munich;

4. Clinical Cooperation Group Hematopoietic Cell Transplantation, Helmholtz Zentrum München and Department of Medicine III, Ludwig-Maximilians-Universität, Munich;

5. Department of Virology, Max-von-Pettenkofer Institute, Ludwig-Maximilians-Universität, Munich;

6. Clinical Cooperation Group Pediatric Tumor Immunology, Helmholtz Zentrum München and Technische Universität München, Munich; and

7. Institute of Molecular Immunology, Helmholtz Zentrum München, Munich, Germany

Abstract

AbstractPosttransplantation lymphoproliferative disease (PTLD) associated with Epstein-Barr virus (EBV) is a life-threatening complication after allogeneic hematopoietic stem cell transplantation. PTLD is efficiently prevented by adoptive transfer of EBV-specific T cells from the donor. To make EBV-specific T cells available in urgent clinical situations, we developed a rapid protocol for their isolation by overnight stimulation of donor blood cells with peptides derived from 11 EBV antigens, interferon-γ surface capture, and immunomagnetic separation. Six patients with PTLD received 1 transfusion of EBV-specific T cells. No response was seen in 3 patients who had late-stage disease with multiorgan dysfunction at the time of T-cell transfer. In 3 patients who received T cells at an earlier stage of disease, we observed complete and stable remission of PTLD. Two patients have remained free from EBV-associated disease for more than 2 years. CD8+ T cells specific for EBV early antigens rapidly expanded after T-cell transfer, temporarily constituted greater than 20% of all peripheral blood lymphocytes, and were maintained throughout the observation period. Thus, a rapid and sustained reconstitution of a protective EBV-specific T-cell memory occurred after the infusion of small numbers of directly isolated EBV-specific T cells.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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