Targeting CD79b for Chimeric Antigen Receptor T-Cell Therapy of B-Cell Lymphomas

Target Oncol. 2020 Jun;15(3):365-375. doi: 10.1007/s11523-020-00729-7.

Abstract

Background: Although chimeric antigen receptor (CAR) T-cell therapy targeting antigens expressed in refractory and relapsed non-Hodgkin B-cell lymphoma, such as CD19 and CD22, has achieved encouraging clinical effects, some patients fail to attain remission, or relapse after CAR T-cell therapy, which has been ascribed to the loss of the target antigens.

Objective: To evaluate CD79b as an alternative target for CAR T-cell B-cell lymphoma therapy.

Patient and methods: The expression of CD79b in different B-cell lymphomas was determined. Anti-CD79b CAR T-cells expressing one of two different CARs were generated, and a series of in vitro and in vivo experiments were conducted to assess the CAR T-cell function.

Results: We found that CD79b was extensively expressed on the tumor cells of patients with various types of lymphoma regardless of stage, subtype, and cytogenetic and molecular features. Anti-CD79b CAR T-cells were highly specific and effective for the treatment of B-cell lymphomas.

Conclusions: Our data indicate that CD79b could be used as a target for CAR T-cell therapy of B-cell lymphomas, and further clinical development is warranted.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CD79 Antigens / metabolism*
  • Cell Line, Tumor
  • Female
  • Humans
  • Lymphoma, B-Cell / genetics*
  • Mice
  • Receptors, Chimeric Antigen / metabolism*
  • Transfection

Substances

  • CD79 Antigens
  • CD79B protein, human
  • Receptors, Chimeric Antigen