Preclinical and clinical advances in dual-target chimeric antigen receptor therapy for hematological malignancies

In recent years, the excellent curative effect of CD19-specific chimeric antigen receptor (CAR) T-cell therapy has brought hope to patients with relapsing or refractory B-cell hematological malignancies, however relapse after CAR T-cell infusion has hindered the widespread clinical application of this immunotherapy and targeted antigen-negative relapse has caused widespread concern. Consequently, strategies for increasing targeted antigens have been created. In addition to the most widely applied target, namely CD19, researchers have further explored the possibility of other targets, such as CD20, CD22, CD33, and CD123, and have tested a series of combination antigen CAR T-cell therapies. Here, we summarize the current preclinical and clinical studies of dual-target CAR T cells.

Automated summary

CD19-specific CAR T-cell therapy has shown significant efficacy in treating B-cell hematological malignancies, but targeted antigen-negative relapse poses a challenge to its widespread application. Researchers have explored alternative targets and tested combination antigen CAR T-cell therapies to enhance treatment effectiveness.