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本文引用的文献

1
Analyses of HLA-C-specific KIR repertoires in donors with group A and B haplotypes suggest a ligand-instructed model of NK cell receptor acquisition.对具有 A 组和 B 组单倍型的供体中 HLA-C 特异性 KIR 库的分析表明 NK 细胞受体获得的配体指导模型。
Blood. 2011 Jan 6;117(1):98-107. doi: 10.1182/blood-2010-03-273656. Epub 2010 Oct 8.
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Bispecific antibodies for cancer therapy: the light at the end of the tunnel?双特异性抗体在癌症治疗中的应用:隧道尽头的曙光?
MAbs. 2009 Nov-Dec;1(6):539-47. doi: 10.4161/mabs.1.6.10015.
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Generation of bispecific and tandem diabodies.双特异性和串联双抗体的生成。
Methods Mol Biol. 2009;562:177-93. doi: 10.1007/978-1-60327-302-2_14.
4
Immunotherapy of lymphoma and leukemia with T-cell engaging BiTE antibody blinatumomab.用T细胞衔接双特异性T细胞衔接器(BiTE)抗体博纳吐单抗对淋巴瘤和白血病进行免疫治疗。
Leuk Lymphoma. 2009 Jun;50(6):886-91. doi: 10.1080/10428190902943077.
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Tumor regression in cancer patients by very low doses of a T cell-engaging antibody.极低剂量的T细胞结合抗体使癌症患者肿瘤消退。
Science. 2008 Aug 15;321(5891):974-7. doi: 10.1126/science.1158545.
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Strictly target cell-dependent activation of T cells by bispecific single-chain antibody constructs of the BiTE class.严格依赖靶细胞的BiTE类双特异性单链抗体构建体对T细胞的激活。
J Immunother. 2007 Nov-Dec;30(8):798-807. doi: 10.1097/CJI.0b013e318156750c.
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Bispecific antibodies: molecules that enable novel therapeutic strategies.双特异性抗体:实现新型治疗策略的分子。
Pathobiology. 2007;74(1):3-14. doi: 10.1159/000101046.
8
T-cell activation and B-cell depletion in chimpanzees treated with a bispecific anti-CD19/anti-CD3 single-chain antibody construct.用双特异性抗CD19/抗CD3单链抗体构建体治疗的黑猩猩中的T细胞活化和B细胞耗竭。
Cancer Immunol Immunother. 2006 May;55(5):503-14. doi: 10.1007/s00262-005-0001-1. Epub 2005 Jul 20.
9
Effective lysis of lymphoma cells with a stabilised bispecific single-chain Fv antibody against CD19 and FcgammaRIII (CD16).用一种针对CD19和FcγRIII(CD16)的稳定双特异性单链Fv抗体有效裂解淋巴瘤细胞。
Br J Haematol. 2005 Jul;130(2):218-28. doi: 10.1111/j.1365-2141.2005.05414.x.
10
Serial killing of tumor cells by cytotoxic T cells redirected with a CD19-/CD3-bispecific single-chain antibody construct.用CD19-/CD3-双特异性单链抗体构建体重定向的细胞毒性T细胞对肿瘤细胞的连续杀伤作用
Int J Cancer. 2005 May 20;115(1):98-104. doi: 10.1002/ijc.20908.

B 细胞 NHL 患者的 T 和 NK 细胞在结合双特异性四价抗体 CD19×CD3 或 CD19×CD16 后对淋巴瘤细胞发挥细胞毒性作用。

T and NK cells of B cell NHL patients exert cytotoxicity against lymphoma cells following binding of bispecific tetravalent antibody CD19 × CD3 or CD19 × CD16.

机构信息

Department of Hematology, Oncology and Clinical Immunology, Heinrich-Heine-University, Düsseldorf, Germany.

出版信息

Cancer Immunol Immunother. 2012 Oct;61(10):1869-75. doi: 10.1007/s00262-012-1339-9. Epub 2012 Sep 14.

DOI:10.1007/s00262-012-1339-9
PMID:22976535
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11028742/
Abstract

Bispecific tetravalent antibodies (TandAb) directed against the B cell surface marker CD19 and activating receptors on T or NK cells (CD19 × CD3 or CD19 × CD16) have shown promising effects in vitro and in preclinical studies. Here, we examine the cytotoxic efficacy of T and NK cells from patients with B cell Non-Hodgkin's Lymphoma (NHL) against B-lymphoma cells following the binding of the matching TandAb. The addition of CD19 × CD16 TandAb led to a threefold increase in NK cell activation in the presence of B-lymphoma cells. Similarly, T cells displayed a sevenfold increase in cytotoxic activity after the addition of CD19 × CD3 TandAb. Comparison of T and NK cell effector function of patients and healthy controls showed comparable levels of cytotoxic activity in response to lymphoma cells and no reduction in functional activity due to age, disease stage or the type and amount of previous therapy. Thus, T and NK cells of patients with B cell NHL are fully capable of being activated by therapeutic crosslinking antibodies. These results provide a rationale for the use of TandAbs for patients with B cell NHL, particularly in cases where remission with minimal residual disease could be achieved by cytotoxic chemotherapy.

摘要

双特异性四价抗体(TandAb)针对 B 细胞表面标志物 CD19 和 T 或 NK 细胞上的激活受体(CD19×CD3 或 CD19×CD16),在体外和临床前研究中显示出有希望的效果。在这里,我们研究了源自 B 细胞非霍奇金淋巴瘤(NHL)患者的 T 和 NK 细胞在结合匹配的 TandAb 后对 B 淋巴瘤细胞的细胞毒性功效。在存在 B 淋巴瘤细胞的情况下,添加 CD19×CD16 TandAb 导致 NK 细胞激活增加了三倍。同样,添加 CD19×CD3 TandAb 后,T 细胞的细胞毒性活性增加了七倍。比较患者和健康对照者的 T 和 NK 细胞效应功能表明,对淋巴瘤细胞的细胞毒性活性水平相当,并且由于年龄、疾病阶段或先前治疗的类型和数量,功能活性没有降低。因此,B 细胞 NHL 患者的 T 和 NK 细胞完全能够被治疗性交联抗体激活。这些结果为 B 细胞 NHL 患者使用 TandAb 提供了依据,特别是在通过细胞毒性化疗可以达到最小残留疾病缓解的情况下。