# Overcoming Resistance and Relapse in CAR-T and CAR-NK Cell Therapies: From Bench to Bedside

**Authors:** Yuhe Wang, Wenxia Shao, Jianhua Mao, Qing Ye

PMC · DOI: 10.34133/research.1068 · 2026-01-05

## TL;DR

This paper reviews the challenges of resistance and relapse in CAR-T and CAR-NK cell therapies for blood cancers and explores ways to improve their effectiveness.

## Contribution

The paper provides a comprehensive review of resistance mechanisms and therapeutic strategies in CAR-T and CAR-NK therapies.

## Key findings

- CAR-T and CAR-NK therapies are effective against hematologic malignancies like leukemia and lymphoma.
- Resistance and recurrence involve factors like target cells, CAR cell traits, and immune suppression.
- The paper explores current strategies and future directions to overcome these challenges.

## Abstract

As pioneering immunotherapy approaches, chimeric antigen receptor T cell (CAR-T) and natural killer cell (CAR-NK) therapies have shown notable clinical effectiveness when addressing different kinds of hematologic malignancies. For example, the application and efficacy of CAR-T cell therapy in acute lymphocytic leukemia, large B cell lymphoma, mantle cell lymphoma, and multiple myeloma have been widely recognized. In addition, the safety and feasibility of CAR-NK therapy when used to treat refractory/recurrent large B cell lymphoma have been verified. In particular, CD19-targeted CAR-T cell therapy has achieved marked efficacy and breakthrough progress in treating relapsed and refractory B cell leukemia and lymphoma. Although CAR-T cell therapy has achieved significant effectiveness in treating these diseases, patients still face challenges, including primary resistance and secondary recurrence after treatment. The complex mechanisms of resistance and recurrence involve multiple factors, such as target cells, CAR cell characteristics, and immune suppression conditions. This review examines resistance and recurrence mechanisms in CAR-T and CAR-NK therapies while exploring current therapeutic strategies and future research directions.

## Linked entities

- **Diseases:** acute lymphocytic leukemia (MONDO:0004967), large B cell lymphoma (MONDO:0968974), mantle cell lymphoma (MONDO:0018876), multiple myeloma (MONDO:0009693), B cell lymphoma (MONDO:0015759)

## Full-text entities

- **Genes:** CXADRP1 (CXADR pseudogene 1) [NCBI Gene 653108] {aka CAR, CXADRP}, CD19 (CD19 molecule) [NCBI Gene 930] {aka B4, CVID3}
- **Diseases:** B cell leukemia and lymphoma (MESH:D015448), acute lymphocytic leukemia (MESH:D054198), multiple myeloma (MESH:D009101), large B cell lymphoma (MESH:D016393), mantle cell lymphoma (MESH:D020522), hematologic malignancies (MESH:D019337)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12766706/full.md

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Source: https://tomesphere.com/paper/PMC12766706