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本文引用的文献

1
Immune checkpoint inhibitors and the shared epitope theory: from hypothesis to practice.免疫检查点抑制剂与共同表位理论:从假说到实践
Transl Cancer Res. 2019 Dec;8(Suppl 6):S625-S627. doi: 10.21037/tcr.2019.07.43.
2
Toxicity of tumor immune checkpoint inhibitors-more attention should be paid.肿瘤免疫检查点抑制剂的毒性——应予以更多关注。
Transl Lung Cancer Res. 2019 Dec;8(6):1125-1133. doi: 10.21037/tlcr.2019.11.26.
3
Clinical efficacy and safety of anti-PD-1/PD-L1 treatments in non-small cell lung cancer (NSCLC).抗 PD-1/PD-L1 治疗在非小细胞肺癌(NSCLC)中的临床疗效和安全性。
Artif Cells Nanomed Biotechnol. 2019 Dec;47(1):4194-4201. doi: 10.1080/21691401.2019.1687499.
4
Checkpoint inhibitor-associated autoimmunity.检查点抑制剂相关性自身免疫。
Best Pract Res Clin Rheumatol. 2018 Dec;32(6):781-802. doi: 10.1016/j.berh.2019.03.009. Epub 2019 Apr 15.
5
Nivolumab-induced hepatitis: A rare side effect of an immune check point inhibitor.纳武单抗诱发的肝炎:一种免疫检查点抑制剂的罕见副作用。
J Oncol Pharm Pract. 2020 Mar;26(2):459-461. doi: 10.1177/1078155219837342. Epub 2019 Mar 25.
6
Acute liver injury in the context of immune checkpoint inhibitor-related colitis treated with infliximab.免疫检查点抑制剂相关性结肠炎治疗中使用英夫利昔单抗导致的急性肝损伤。
J Immunother Cancer. 2019 Feb 18;7(1):47. doi: 10.1186/s40425-019-0532-1.
7
Safety and Efficacy of Re-treating with Immunotherapy after Immune-Related Adverse Events in Patients with NSCLC.非小细胞肺癌患者发生免疫相关不良事件后再次使用免疫治疗的安全性和疗效。
Cancer Immunol Res. 2018 Sep;6(9):1093-1099. doi: 10.1158/2326-6066.CIR-17-0755. Epub 2018 Jul 10.
8
Nivolumab in pretreated non-small cell lung cancer: continuing the immunolution.纳武利尤单抗用于经治非小细胞肺癌:免疫治疗的持续探索
Transl Lung Cancer Res. 2018 Apr;7(Suppl 2):S91-S94. doi: 10.21037/tlcr.2018.01.14.
9
Immunotherapy in surgically resectable non-small cell lung cancer.可手术切除的非小细胞肺癌的免疫治疗
J Thorac Dis. 2018 Feb;10(Suppl 3):S404-S411. doi: 10.21037/jtd.2017.12.93.
10
Uncoupling therapeutic from immunotherapy-related adverse effects for safer and effective anti-CTLA-4 antibodies in CTLA4 humanized mice.在 CTLA4 人源化小鼠中,为了更安全有效地使用抗 CTLA-4 抗体,需要将治疗相关不良反应与免疫治疗相关不良反应区分开来。
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低蛋白血症是免疫治疗相关肝功能障碍的一种表现。

Hypoproteinemia being a manifestation of immunotherapy-related liver dysfunction.

作者信息

Deng Juan, Chen Xiaoxia, Sun Hui, Liu Yu, Li Wei, Chen Bin, Zhao Sha, Jia Keyi, Wang Hao, Guo Haoyue, Jiang Minlin, Xu Yi, He Yayi, Zhou Caicun

机构信息

Department of Medical Oncology, Shanghai Pulmonary Hospital, Tongji University Medical School Cancer Institute, Tongji University School of Medicine, Shanghai, China.

Tongji University, Shanghai, China.

出版信息

Ann Transl Med. 2020 Jul;8(14):889. doi: 10.21037/atm-20-4980.

DOI:10.21037/atm-20-4980
PMID:32793733
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7396795/
Abstract

Immunotherapy has changed the pattern of treatment in cancer. The interaction between programmed death-1 (PD-1) and programmed death-ligand 1 (PD-L1) inhibits the activation of T cells, and PD-1/PD-L1 inhibitors can increase the immune response to cancer cells by inducing the immune cells, which has become an important clinical method to treat cancer. However, the alteration in the activation of T cells might lead to misidentification between the body's own cells and tumor cells and induce immune-related adverse events (IRAEs), such as pneumonitis, liver dysfunction, rash, colitis, nephritis, and endocrinopathies. And the IRAEs might lead to serious consequences. Studies have reported that PD-1/PD-L1 inhibitor-related hepatotoxicity is one of these adverse events. Most of the studies reported that hepatitis resulting from PD-1 inhibitor was manifested as elevated liver enzymes and bilirubin. Quite a few patients experienced lower degree of hepatotoxicity treated with checkpoint inhibitors, which indicated that it was necessary to focus on immunotherapy-related liver dysfunction. Here, we report a case of immunotherapy-related liver dysfunction with hypoproteinemia as the first manifestation under the treatment of PD-1 inhibitors combined with chemotherapy. This case suggests that hypoproteinemia was one of the manifestations of immunotherapy-related liver dysfunction, which helps us better understand the immunotherapy-related disease.

摘要

免疫疗法改变了癌症的治疗模式。程序性死亡受体1(PD-1)与程序性死亡配体1(PD-L1)之间的相互作用会抑制T细胞的激活,而PD-1/PD-L1抑制剂可通过诱导免疫细胞来增强对癌细胞的免疫反应,这已成为治疗癌症的一种重要临床方法。然而,T细胞激活的改变可能会导致机体自身细胞与肿瘤细胞之间的误识别,并引发免疫相关不良事件(IRAEs),如肺炎、肝功能障碍、皮疹、结肠炎、肾炎和内分泌病。而且这些免疫相关不良事件可能会导致严重后果。研究报告称,PD-1/PD-L1抑制剂相关的肝毒性就是这些不良事件之一。大多数研究报告称,PD-1抑制剂所致肝炎表现为肝酶和胆红素升高。不少接受检查点抑制剂治疗的患者出现了程度较低的肝毒性,这表明有必要关注免疫疗法相关的肝功能障碍。在此,我们报告1例在PD-1抑制剂联合化疗治疗下以低蛋白血症为首发表现的免疫疗法相关肝功能障碍病例。该病例提示低蛋白血症是免疫疗法相关肝功能障碍的表现之一,这有助于我们更好地理解免疫疗法相关疾病。