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免疫检查点抑制剂与同种异体移植排斥风险:关于其在肾移植受者中应用的新证据

Immune Checkpoint Inhibitors and Allograft Rejection Risk: Emerging Evidence Regarding Their Use in Kidney Transplant Recipients.

作者信息

Khan Muhammad Ali, Mehmood Munir, El Azzazi Hind, Shaikh Samiullah, Bhasin-Chhabra Bhavna, Gudsoorkar Prakash, Nair Sumi Sukumaran, Kodali Lavanya, Mour Girish, Swaminathan Sundararaman, Abu Jawdeh Bassam G

机构信息

Division of Nephrology and Hypertension, Mayo Clinic Arizona, 5777 E. Mayo Blvd, Phoenix, AZ 85054, USA.

Medical College, The Aga Khan University, Stadium Road, Karachi 74800, Pakistan.

出版信息

J Clin Med. 2025 Jul 20;14(14):5152. doi: 10.3390/jcm14145152.

DOI:10.3390/jcm14145152
PMID:40725844
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12295338/
Abstract

The indications for immune checkpoint inhibitor (ICI) use in cancer treatment continue to expand. This is attributable to their proven anticancer activity in addition to their tolerability and favorable toxicity profile as compared to conventional chemotherapeutic agents. ICIs work by blocking the inhibitory signals between tumor cells and T-cells, thereby enhancing the T-cell cytotoxic activity to inhibit tumor growth. Because of their immune-stimulating effect, ICIs are linked to adverse renal outcomes in both native and transplanted kidneys. The risk of kidney allograft rejection in the setting of ICI use has been reported to be around 40%, leading to an increased risk of graft loss. In this report, we review the literature examining outcomes in kidney transplant recipients receiving ICIs for various oncologic indications.

摘要

免疫检查点抑制剂(ICI)在癌症治疗中的应用指征不断扩大。这归因于其已被证实的抗癌活性,以及与传统化疗药物相比的耐受性和良好的毒性特征。ICI通过阻断肿瘤细胞与T细胞之间的抑制信号发挥作用,从而增强T细胞的细胞毒性活性以抑制肿瘤生长。由于其免疫刺激作用,ICI与天然肾和移植肾的不良肾脏结局相关。据报道,在使用ICI的情况下,肾移植受者发生移植肾排斥反应的风险约为40%,导致移植肾丢失风险增加。在本报告中,我们回顾了有关接受ICI治疗各种肿瘤指征的肾移植受者结局的文献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2f/12295338/863bb3e2892a/jcm-14-05152-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2f/12295338/863bb3e2892a/jcm-14-05152-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2f/12295338/863bb3e2892a/jcm-14-05152-g001.jpg

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本文引用的文献

1
Outcomes of Solid Organ Transplant Recipients With Advanced Cancers Receiving Immune Checkpoint Inhibitors: A Systematic Review and Individual Participant Data Meta-Analysis.接受免疫检查点抑制剂治疗的晚期癌症实体器官移植受者的结局:一项系统评价和个体参与者数据荟萃分析。
JAMA Oncol. 2025 Jun 22. doi: 10.1001/jamaoncol.2025.2374.
2
Immune Checkpoint Inhibitor Use in Kidney Transplant Patients: A National Case Series From Ireland.免疫检查点抑制剂在肾移植患者中的应用:来自爱尔兰的全国性病例系列研究
Clin Transplant. 2025 Feb;39(2):e70101. doi: 10.1111/ctr.70101.
3
High density of TCF1+ stem-like tumor-infiltrating lymphocytes is associated with favorable disease-specific survival in NSCLC.
TCF1+ 干细胞样肿瘤浸润淋巴细胞的高密度与非小细胞肺癌中良好的疾病特异性生存率相关。
Front Immunol. 2024 Dec 19;15:1504220. doi: 10.3389/fimmu.2024.1504220. eCollection 2024.
4
Diagnosis and management of immune checkpoint inhibitor-associated nephrotoxicity: a position statement from the American Society of Onco-nephrology.免疫检查点抑制剂相关肾毒性的诊断与管理:美国肿瘤肾脏病学会立场声明
Kidney Int. 2025 Jan;107(1):21-32. doi: 10.1016/j.kint.2024.09.017. Epub 2024 Oct 24.
5
Acute Allograft Rejection in Kidney Transplant Recipients Treated With Immune Checkpoint Inhibitors: An Educational Case Report.免疫检查点抑制剂治疗的肾移植受者急性同种异体移植排斥反应:一例教学病例报告
Can J Kidney Health Dis. 2024 Oct 21;11:20543581241289191. doi: 10.1177/20543581241289191. eCollection 2024.
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Overcoming cold tumors: a combination strategy of immune checkpoint inhibitors.克服冷肿瘤:免疫检查点抑制剂的联合策略。
Front Immunol. 2024 Mar 13;15:1344272. doi: 10.3389/fimmu.2024.1344272. eCollection 2024.
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Rapid Life-Saving Response to Anti-PD-1 in a Solid Organ Transplant Recipient With Metastatic Cutaneous Squamous Cell Carcinoma: A Case Report and Review.实体器官移植受者伴转移性皮肤鳞状细胞癌的抗 PD-1 快速救生反应:病例报告和综述。
J Immunother. 2024;47(6):216-219. doi: 10.1097/CJI.0000000000000514. Epub 2024 Mar 27.
8
Thyroid disorders induced by immune checkpoint inhibitors.免疫检查点抑制剂引起的甲状腺疾病。
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Cemiplimab for Kidney Transplant Recipients With Advanced Cutaneous Squamous Cell Carcinoma.西妥昔单抗治疗晚期皮肤鳞状细胞癌肾移植受者。
J Clin Oncol. 2024 Mar 20;42(9):1021-1030. doi: 10.1200/JCO.23.01498. Epub 2024 Jan 22.