CAR-T Engager proteins optimize anti-CD19 CAR-T cell therapies for lymphoma

Oncoimmunology. 2022 Aug 17;11(1):2111904. doi: 10.1080/2162402X.2022.2111904. eCollection 2022.

Abstract

B cell lymphoma therapy has been transformed by CD19-targeting cellular therapeutics that induce high clinical response rates and impressive remissions in relapsed and refractory patients. However, approximately half of all patients who respond to CD19-directed cell therapy relapse, the majority within 6 months. One characteristic of relapse is loss or reduction of CD19 expression on malignant B cells. We designed a unique therapeutic to prevent and reverse relapses due to lost or reduced CD19 expression. This novel biologic, a CAR T Engager, binds CD20 and displays the CD19 extracellular domain. This approach increases the apparent CD19 antigen density on CD19-positive/CD20-positive lymphoma cells, and prevents antigen-loss induced relapse, as CD19 bound to CD20 remains present on the cell surface. We demonstrate that this novel therapeutic prevents and reverses lymphoma relapse in vitro and prevents CD19-negative lymphoma growth and relapse in vivo.

Keywords: CAR T cells; CD19; CD20; Engager protein; lymphoma; relapse.

MeSH terms

  • Antigens, CD19
  • Antigens, CD20
  • Humans
  • Lymphoma* / therapy
  • Neoplasm Recurrence, Local
  • Receptors, Antigen, T-Cell
  • Receptors, Chimeric Antigen*
  • T-Lymphocytes

Substances

  • Antigens, CD19
  • Antigens, CD20
  • Receptors, Antigen, T-Cell
  • Receptors, Chimeric Antigen

Grants and funding

The author(s) reported there is no funding associated with the work featured in this article.