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CD8+ 细胞毒性 T 淋巴细胞和组织驻留记忆细胞的一个分支在非腔乳腺癌中的潜在作用。

The potential role of CD8+ cytotoxic T lymphocytes and one branch connected with tissue-resident memory in non-luminal breast cancer.

机构信息

Department of Breast Cancer, The First Affiliated Hospital of Dalian Medical University, Dalian, Liaoning Province, China.

出版信息

PeerJ. 2024 Jul 10;12:e17667. doi: 10.7717/peerj.17667. eCollection 2024.

DOI:10.7717/peerj.17667
PMID:39006029
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11246025/
Abstract

Advances in understanding the pathological mechanisms of breast cancer have resulted in the emergence of novel therapeutic strategies. However, triple-negative breast cancer (TNBC), a molecular subtype of breast cancer with a poor prognosis, lacks classical and general therapeutic targets, hindering the clinical application of several therapies to breast cancer. As insights into the unique immunity and molecular mechanisms of TNBC have become more extensive, immunotherapy has gradually become a valuable complementary approach to classical radiotherapy and chemotherapy. CD8+ cells are significant actors in the tumor immunity cycle; thus, research on TNBC immunotherapy is increasingly focused in this direction. Recently, CD8+ tissue-resident memory (TRM) cells, a subpopulation of CD8+ cells, have been explored in relation to breast cancer and found to seemingly play an undeniably important role in tumor surveillance and lymphocytic infiltration. In this review, we summarize the recent advances in the mechanisms and relative targets of CD8+ T cells, and discuss the features and potential applications of CD8+ TRM cells in non-luminal breast cancer immunotherapy.

摘要

对乳腺癌病理机制的深入理解催生了新的治疗策略。然而,三阴性乳腺癌(TNBC)作为乳腺癌的一种分子亚型,预后较差,缺乏经典和通用的治疗靶点,阻碍了几种针对乳腺癌的疗法的临床应用。随着对 TNBC 独特免疫和分子机制的认识不断深入,免疫疗法逐渐成为经典放化疗的一种有价值的补充方法。CD8+细胞是肿瘤免疫周期中的重要执行者;因此,TNBC 免疫疗法的研究越来越集中在这一方向。最近,CD8+组织驻留记忆(TRM)细胞作为 CD8+细胞的一个亚群,与乳腺癌的关系已被探索,并被发现似乎在肿瘤监测和淋巴细胞浸润中发挥着不可否认的重要作用。在这篇综述中,我们总结了 CD8+T 细胞的作用机制和相关靶点的最新进展,并讨论了 CD8+TRM 细胞在非腔性乳腺癌免疫治疗中的特征和潜在应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20f9/11246025/d639134ec3eb/peerj-12-17667-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20f9/11246025/2cf42267a56b/peerj-12-17667-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20f9/11246025/28dbd646b604/peerj-12-17667-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20f9/11246025/d639134ec3eb/peerj-12-17667-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20f9/11246025/2cf42267a56b/peerj-12-17667-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20f9/11246025/28dbd646b604/peerj-12-17667-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20f9/11246025/d639134ec3eb/peerj-12-17667-g003.jpg

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本文引用的文献

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Cell Stem Cell. 2024 Jul 5;31(7):989-1002.e9. doi: 10.1016/j.stem.2024.04.018. Epub 2024 May 15.
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Thermo-immune synergy: Camrelizumab plus microwave ablation in preoperative early-stage breast cancer.
热免疫协同作用:卡瑞利珠单抗联合微波消融治疗早期乳腺癌术前新辅助治疗。
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Targeting the activated microenvironment with endosialin (CD248)-directed CAR-T cells ablates perivascular cells to impair tumor growth and metastasis.靶向激活的微环境中的内皮细胞唾液酸糖蛋白 8(CD248),通过 CAR-T 细胞消除血管周细胞,以抑制肿瘤生长和转移。
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A SOX9-B7x axis safeguards dedifferentiated tumor cells from immune surveillance to drive breast cancer progression.SOX9-B7x 轴保护去分化的肿瘤细胞免受免疫监视,从而推动乳腺癌的进展。
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Targeting sphingosine 1-phosphate receptor 3 inhibits T-cell exhaustion and regulates recruitment of proinflammatory macrophages to improve antitumor efficacy of CAR-T cells against solid tumor.靶向鞘氨醇 1-磷酸受体 3 抑制 T 细胞耗竭并调节促炎巨噬细胞的募集,以提高 CAR-T 细胞对实体瘤的抗肿瘤疗效。
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