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回到第一讲:儿童癌症的主要组织相容性复合体与免疫疗法。

Going back to class I: MHC and immunotherapies for childhood cancer.

作者信息

Haworth Kellie B, Leddon Jennifer L, Chen Chun-Yu, Horwitz Edwin M, Mackall Crystal L, Cripe Timothy P

机构信息

Division of Hematology/Oncology/Blood and Marrow Transplant, Nationwide Children's Hospital, Columbus, Ohio.

出版信息

Pediatr Blood Cancer. 2015 Apr;62(4):571-6. doi: 10.1002/pbc.25359. Epub 2014 Dec 18.

DOI:10.1002/pbc.25359
PMID:25524394
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4339346/
Abstract

After decades of unfulfilled promise, immunotherapies for cancer have reached a tipping point, with several FDA approved products now on the market and many more showing promise in both adult and pediatric clinical trials. Tumor cell expression of MHC class I has emerged as a potential determinant of the therapeutic success of many immunotherapy approaches. Here we review current knowledge regarding MHC class I expression in pediatric cancers including a discussion of prognostic significance, the opposing influence of MHC on T-cell versus NK-mediated therapies, and strategies to reverse or circumvent MHC down-regulation.

摘要

经过数十年未实现的承诺,癌症免疫疗法已达到一个转折点,目前有几种获得美国食品药品监督管理局(FDA)批准的产品上市,还有更多产品在成人和儿科临床试验中显示出前景。肿瘤细胞I类主要组织相容性复合体(MHC)的表达已成为许多免疫疗法治疗成功的潜在决定因素。在此,我们综述了有关儿科癌症中MHC I类表达的现有知识,包括对预后意义的讨论、MHC对T细胞与自然杀伤(NK)细胞介导疗法的相反影响,以及逆转或规避MHC下调的策略。

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本文引用的文献

1
Cancer testis antigen and immunotherapy.癌睾丸抗原与免疫疗法。
Immunotargets Ther. 2013 Apr 17;2:11-9. doi: 10.2147/ITT.S35570. eCollection 2013.
2
Improving the outcome of leukemia by natural killer cell-based immunotherapeutic strategies.通过基于自然杀伤细胞的免疫治疗策略改善白血病的治疗效果。
Front Immunol. 2014 Mar 17;5:95. doi: 10.3389/fimmu.2014.00095. eCollection 2014.
3
Childhood and adolescent cancer statistics, 2014.儿童和青少年癌症统计数据,2014 年。
Med23 缺乏可重新编程肿瘤微环境以促进肺肿瘤发生。
Br J Cancer. 2024 Mar;130(5):716-727. doi: 10.1038/s41416-023-02556-9. Epub 2024 Jan 9.
4
Non-cellular immunotherapies in pediatric central nervous system tumors.儿科中枢神经系统肿瘤的非细胞免疫疗法。
Front Immunol. 2023 Oct 11;14:1242911. doi: 10.3389/fimmu.2023.1242911. eCollection 2023.
5
Adoptive cell therapy in paediatric extracranial solid tumours: current approaches and future challenges.儿童颅外实体瘤的过继细胞治疗:当前方法和未来挑战。
Eur J Cancer. 2023 Nov;194:113347. doi: 10.1016/j.ejca.2023.113347. Epub 2023 Sep 18.
6
The interaction between osteosarcoma and other cells in the bone microenvironment: From mechanism to clinical applications.骨肉瘤与骨微环境中其他细胞之间的相互作用:从机制到临床应用
Front Cell Dev Biol. 2023 May 3;11:1123065. doi: 10.3389/fcell.2023.1123065. eCollection 2023.
7
Efficacy of Nivolumab in Pediatric Cancers with High Mutation Burden and Mismatch Repair Deficiency.高突变负荷和错配修复缺陷的儿科癌症中纳武单抗的疗效。
Clin Cancer Res. 2023 Dec 1;29(23):4770-4783. doi: 10.1158/1078-0432.CCR-23-0411.
8
Epigenetic therapies for neuroblastoma: immunogenicity awakens.神经母细胞瘤的表观遗传学治疗:免疫原性被唤醒。
Mol Oncol. 2023 May;17(5):718-721. doi: 10.1002/1878-0261.13404. Epub 2023 Mar 8.
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CA Cancer J Clin. 2014 Mar-Apr;64(2):83-103. doi: 10.3322/caac.21219. Epub 2014 Jan 31.
4
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6
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7
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Leukemia. 2014 Apr;28(4):917-27. doi: 10.1038/leu.2013.279. Epub 2013 Sep 26.