Derivation of human T lymphocytes from cord blood and peripheral blood with antiviral and antileukemic specificity from a single culture as protection against infection and relapse after stem cell transplantation

Blood. 2010 Apr 1;115(13):2695-703. doi: 10.1182/blood-2009-09-242263. Epub 2010 Jan 28.

Abstract

Viral infections and leukemic relapse account for the majority of treatment failures in patients with B-cell acute lymphoblastic leukemia (B-ALL) receiving allogeneic hematopoietic stem cell (HSC) or cord blood (CB) transplants. Adoptive transfer of virus-specific cytotoxic T lymphocytes (CTLs) provides protection against common viruses causing serious infections after HSC transplantation without concomitant graft-versus-host disease. We have now generated CTL lines from peripheral blood (PB) or CB units that recognize multiple common viruses and provide antileukemic activity by transgenic expression of a chimeric antigen receptor (CAR) targeting CD19 expressed on B-ALL. PB-derived CAR(+) CTLs produced interferon-gamma (IFNgamma) in response to cytomegalovirus-pp65, adenovirus-hexon, and Epstein-Barr virus pepmixes (from 205 +/- 104 to 1034 +/- 304 spot-forming cells [SFCs]/10(5) T cells) and lysed primary B-ALL blasts in (51)Cr-release assays (mean, 66% +/- 5% specific lysis; effector-target [E/T] ratio, 40:1) and the CD19(+) Raji cell line (mean, 78% +/- 17%) in contrast to nontransduced controls (8% +/- 8% and 3% +/- 2%). CB-derived CAR(+) CTLs showed similar antiviral and antitumor function and both PB and CB CAR(+) CTLs completely eliminated B-ALL blasts over 5 days of coculture. This approach may prove beneficial for patients with high-risk B-ALL who have recently received an HSC or CB transplant and are at risk of infection and relapse.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoviridae / immunology
  • Adoptive Transfer*
  • Adult
  • Antigens, CD19 / immunology
  • Antigens, Viral / immunology
  • Blood Cells / immunology
  • Cell Line, Transformed
  • Cell Line, Tumor / immunology
  • Cells, Cultured / immunology
  • Cells, Cultured / transplantation
  • Coxsackie and Adenovirus Receptor-Like Membrane Protein
  • Cytomegalovirus / immunology
  • Feasibility Studies
  • Fetal Blood / cytology*
  • Humans
  • In Vitro Techniques
  • Interferon-gamma / biosynthesis
  • Leukemia, B-Cell / immunology*
  • Leukemia, B-Cell / pathology
  • Neoplastic Stem Cells / immunology
  • Postoperative Complications / prevention & control*
  • Postoperative Complications / virology
  • Receptors, Antigen, T-Cell, alpha-beta / immunology
  • Receptors, Virus / genetics
  • Receptors, Virus / physiology*
  • Recombinant Fusion Proteins / biosynthesis
  • Recombinant Fusion Proteins / immunology
  • Recurrence
  • Single-Chain Antibodies / genetics
  • Single-Chain Antibodies / immunology*
  • T-Lymphocyte Subsets / cytology
  • T-Lymphocyte Subsets / immunology*
  • T-Lymphocyte Subsets / transplantation
  • T-Lymphocytes, Cytotoxic / cytology
  • T-Lymphocytes, Cytotoxic / immunology*
  • T-Lymphocytes, Cytotoxic / transplantation
  • Virus Diseases / immunology
  • Virus Diseases / prevention & control*

Substances

  • Antigens, CD19
  • Antigens, Viral
  • CLMP protein, human
  • Coxsackie and Adenovirus Receptor-Like Membrane Protein
  • Receptors, Antigen, T-Cell, alpha-beta
  • Receptors, Virus
  • Recombinant Fusion Proteins
  • Single-Chain Antibodies
  • Interferon-gamma