# The impact of immune cells selection on the therapeutic efficacy of CAR-T cell therapy

**Authors:** 文昕 齐, 伟龙 张, 红梅 景

PMC · DOI: 10.3760/cma.j.cn121090-20240321-00104 · Chinese Journal of Hematology · 2024-07-01

## TL;DR

This paper explores how selecting specific immune cells can improve the effectiveness of CAR-T cell therapy for cancer treatment.

## Contribution

The study highlights novel immune cell sources and strategies to enhance CAR-T cell efficacy and reduce side effects.

## Key findings

- CAR-T cells derived from umbilical cord blood and induced pluripotent stem cells show enhanced tumor-killing ability.
- Using virus-specific T cells and γδT cells helps reduce graft-versus-host disease in CAR-T therapy.
- Blocking T cell exhaustion through immune checkpoint inhibitors improves CAR-T cell performance.

## Abstract

从免疫细胞层面总结了各种新型嵌合抗原受体T细胞（CAR-T细胞）疗法，健康年轻受试者的T细胞、干性记忆样T细胞、人体诱导多能干细胞、脐带血T细胞来源的CAR-T细胞疗法可增强肿瘤杀伤效应。从通用型CAR细胞方面，病毒特异性T细胞、γδT细胞、iNKT细胞、巨噬细胞等能有效减轻移植物抗宿主病反应。此外，增强去白细胞过程中单核细胞的清除、保持CD4+/CD8+ T细胞均衡比例等策略也是增强CAR-T细胞扩增及杀伤效力的方法。细胞耗竭标志物高表达的T细胞对CAR-T细胞的转导、扩增及发挥杀伤效力等会产生负向影响，使用免疫检查点阻断剂等方式抑制T细胞耗竭能提高CAR-T细胞作用效应。

## Linked entities

- **Diseases:** cancer (MONDO:0004992)

## Full-text entities

- **Genes:** HLA-C (major histocompatibility complex, class I, C) [NCBI Gene 3107] {aka D6S204, HLA-JY3, HLAC, HLC-C, MHC, PSORS1}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}
- **Diseases:** tumor (MESH:D009369)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** CAR-T — Mus musculus (Mouse), Transformed cell line (CVCL_WN86)

## Full text

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## Figures

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## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC11388120/full.md

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Source: https://tomesphere.com/paper/PMC11388120