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本文引用的文献

1
B7-H3: An Attractive Target for Antibody-based Immunotherapy.B7-H3:抗体免疫治疗的一个有吸引力的靶点。
Clin Cancer Res. 2021 Mar 1;27(5):1227-1235. doi: 10.1158/1078-0432.CCR-20-2584. Epub 2020 Oct 13.
2
NK-Cell-Mediated Targeting of Various Solid Tumors Using a B7-H3 Tri-Specific Killer Engager In Vitro and In Vivo.使用B7-H3三特异性杀伤衔接子在体外和体内对多种实体瘤进行自然杀伤细胞介导的靶向治疗
Cancers (Basel). 2020 Sep 18;12(9):2659. doi: 10.3390/cancers12092659.
3
High B7-H3 expression is linked to increased risk of prostate cancer progression.高 B7-H3 表达与前列腺癌进展风险增加相关。
Pathol Int. 2020 Oct;70(10):733-742. doi: 10.1111/pin.12999. Epub 2020 Aug 10.
4
B7-H3 is spliced by SRSF3 in colorectal cancer.B7-H3 在结直肠癌中通过 SRSF3 拼接。
Cancer Immunol Immunother. 2021 Feb;70(2):311-321. doi: 10.1007/s00262-020-02683-9. Epub 2020 Jul 27.
5
B7-H3 immune checkpoint expression is a poor prognostic factor in colorectal carcinoma.B7-H3 免疫检查点表达是结直肠癌的一个预后不良因素。
Mod Pathol. 2020 Nov;33(11):2330-2340. doi: 10.1038/s41379-020-0587-z. Epub 2020 Jun 8.
6
Blocking PD-1/PD-L1 by an ADCC enhanced anti-B7-H3/PD-1 fusion protein engages immune activation and cytotoxicity.阻断 PD-1/PD-L1 可通过 ADCC 增强的抗 B7-H3/PD-1 融合蛋白来激发免疫激活和细胞毒性。
Int Immunopharmacol. 2020 Jul;84:106584. doi: 10.1016/j.intimp.2020.106584. Epub 2020 May 15.
7
B7-H3 inhibits the IFN-γ-dependent cytotoxicity of Vγ9Vδ2 T cells against colon cancer cells.B7-H3 抑制 Vγ9Vδ2 T 细胞针对结肠癌细胞的 IFN-γ 依赖性细胞毒性。
Oncoimmunology. 2020 Apr 14;9(1):1748991. doi: 10.1080/2162402X.2020.1748991. eCollection 2020.
8
B7-H3-Targeted CAR-T Cells Exhibit Potent Antitumor Effects on Hematologic and Solid Tumors.靶向B7-H3的嵌合抗原受体T细胞对血液系统肿瘤和实体瘤显示出强大的抗肿瘤作用。
Mol Ther Oncolytics. 2020 Apr 7;17:180-189. doi: 10.1016/j.omto.2020.03.019. eCollection 2020 Jun 26.
9
Expression and Significance of Immune Checkpoints in Clear Cell Carcinoma of the Uterine Cervix.免疫检查点在子宫颈透明细胞癌中的表达及意义。
J Immunol Res. 2020 Apr 3;2020:1283632. doi: 10.1155/2020/1283632. eCollection 2020.
10
Efficacy of B7-H3-Redirected BiTE and CAR-T Immunotherapies Against Extranodal Nasal Natural Killer/T Cell Lymphoma.B7-H3定向双特异性T细胞衔接器(BiTE)和嵌合抗原受体T细胞(CAR-T)免疫疗法治疗结外鼻型自然杀伤/T细胞淋巴瘤的疗效
Transl Oncol. 2020 May;13(5):100770. doi: 10.1016/j.tranon.2020.100770. Epub 2020 Apr 13.

B7-H3 靶向抗体免疫治疗恶性疾病。

B7-H3 targeted antibody-based immunotherapy of malignant diseases.

机构信息

Department of Surgery, Massachusetts General Hospital/Harvard Medical School, Boston, MA, USA.

Department of Orthopaedic Surgery, Massachusetts General Hospital/Harvard Medical School, Boston, MA, USA.

出版信息

Expert Opin Biol Ther. 2021 May;21(5):587-602. doi: 10.1080/14712598.2021.1862791. Epub 2020 Dec 21.

DOI:10.1080/14712598.2021.1862791
PMID:33301369
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8087627/
Abstract

: Recent advances in immuno-oncology and bioengineering have rekindled the interest in monoclonal antibody (mAb)-based immunotherapies for malignancies. Crucial for their success is the identification of tumor antigens (TAs) that can serve as targets. B7-H3, a member of the B7 ligand family, represents such a TA. Although its exact functions and receptor(s) remain unclear, B7-H3 has predominantly a pro-tumorigenic effect mainly by suppressing the anti-tumor functions of T-cells.: Initially we present a historical perspective on TA-specific antibodies for diagnosis and treatment of malignancies. Following a description of the TA requirements to be an attractive antibody-based immunotherapy target, we show that B7-H3 fulfills these criteria. We discuss its structure and functions. In a review and pooled analysis, we describe the limited B7-H3 expression in normal tissues and estimate B7-H3 expression frequency in tumors, tumor-associated vasculature and cancer initiating cells (CICs). Lastly, we discuss the association of B7-H3 expression in tumors with poor prognosis.: B7-H3 is an attractive target for mAb-based cancer immunotherapy. B7-H3-targeting strategies are expected to be highly effective and - importantly - safe. To fully exploit the diagnostic and therapeutic potential of B7-H3, its expression in pre-malignant lesions, serum, metastases, and CICs requires further investigation.

摘要

: 免疫肿瘤学和生物工程的最新进展重新点燃了人们对基于单克隆抗体 (mAb) 的恶性肿瘤免疫疗法的兴趣。成功的关键是确定可以作为靶点的肿瘤抗原 (TA)。B7-H3 是 B7 配体家族的成员,代表了这样一种 TA。尽管其确切功能和受体仍不清楚,但 B7-H3 主要通过抑制 T 细胞的抗肿瘤功能发挥促肿瘤作用。: 我们首先介绍了用于诊断和治疗恶性肿瘤的 TA 特异性抗体的历史观点。在描述了作为有吸引力的抗体为基础的免疫治疗靶点的 TA 要求之后,我们表明 B7-H3 满足这些标准。我们讨论了它的结构和功能。在回顾和汇总分析中,我们描述了 B7-H3 在正常组织中的有限表达,并估计了肿瘤、肿瘤相关血管和癌症起始细胞 (CIC) 中 B7-H3 的表达频率。最后,我们讨论了肿瘤中 B7-H3 表达与预后不良的关系。: B7-H3 是 mAb 为基础的癌症免疫治疗的一个有吸引力的靶点。B7-H3 靶向策略预计将非常有效和 - 重要的是 - 安全。为了充分发挥 B7-H3 的诊断和治疗潜力,需要进一步研究其在癌前病变、血清、转移和 CIC 中的表达。