首页> 外文期刊>Cancer Treatment Reviews >Rationale for combination of therapeutic antibodies targeting tumor cells and immune checkpoint receptors: Harnessing innate and adaptive immunity through IgG1 isotype immune effector stimulation
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Rationale for combination of therapeutic antibodies targeting tumor cells and immune checkpoint receptors: Harnessing innate and adaptive immunity through IgG1 isotype immune effector stimulation

机译:靶向肿瘤细胞和免疫检查点受体的治疗性抗体组合的基本原理:通过IgG1同种型免疫效应刺激利用先天生素和适应性免疫

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Highlights ? Cetuximab has immune activity, eg, antibody-dependent cell-mediated cytotoxicity. ? (Pre)clinical evidence supports the clinical relevance of innate/adaptive immunity. ? Tumor targeted mAbs such as cetuximab induce innate?+?adaptive immunity. ? This mechanism can be leveraged by combining cetuximab?+?immunotherapy. ? Checkpoint inhibitors may elicit synergistic immune response with IgG1-isotype mAbs. Abstract Immunoglobulin (Ig) G1 antibodies stimulate antibody-dependent cell-mediated cytotoxicity (ADCC). Cetuximab, an IgG1 isotype monoclonal antibody, is a standard-of-care treatment for locally advanced and recurrent and/or metastatic squamous cell carcinoma of the head and neck (SCCHN) and metastatic colorectal cancer (CRC). Here we review evidence regarding the clinical relevance of cetuximab-mediated ADCC and other immune functions and provide a biological rationale concerning why this property positions cetuximab as an ideal partner for immune checkpoint inhibitors (ICIs) and other emerging immunotherapies. We performed a nonsystematic review of available preclinical and clinical data involving cetuximab-mediated immune activity and combination approaches of cetuximab with other immunotherapies, including ICIs, in SCCHN and CRC. Indeed, cetuximab mediates ADCC activity in the intratumoral space and primes adaptive and innate cellular immunity. However, counterregulatory mechanisms may lead to immunosuppressive feedback loops. Accordingly, there is a strong rationale for combining ICIs with cetuximab for the treatment of advanced tumors, as targeting CTLA-4, PD-1, and PD-L1 can ostensibly overcome these immunosuppressive counter-mechanisms in the tumor microenvironment. Moreover, combining ICIs (or other immunotherapies) with cetuximab is a promising strategy for boosting immune response and enhancing response rates and durability of response. Cetuximab immune activity—including, but not limited to, ADCC—provides a strong rationale for its combination with ICIs or other immunotherapies to synergistically and fully mobilize the adaptive and innate immunity against tumor cells. Ongoing prospective studies will evaluate the clinical effect of these combination regimens and their immune effect in CRC and SCCHN and in other indications.
机译:强调 ?西妥昔单抗具有免疫活性,例如依赖于依赖性细胞介导的细胞毒性。还(前)临床证据支持先天/自适应免疫的临床相关性。还肿瘤靶向mAb,如西妥昔单抗诱导先天+?适应性免疫。还这种机制可以通过组合西妥昔单抗来利用?+ +免疫疗法。还检查点抑制剂可能与IgG1-同种型mAb引发协同免疫应答。摘要免疫球蛋白(IG)G1抗体刺激抗体依赖性细胞介导的细胞毒性(ADCC)。 Cetuximab是一种IgG1同种型单克隆抗体,是用于头部和颈部(SCCHN)和转移性结直肠癌(CRC)的局部晚期和复发性和/或转移鳞状细胞癌的标准治疗方法。在这里,我们审查了关于西汀蛋白介导的ADCC和其他免疫功能的临床相关性的证据,并提供了一个生物学理由,了解该属性将甲磺替昔单抗作为免疫检查点抑制剂(ICIS)和其他新兴免疫治疗的理想伴侣。我们对可用的临床前和临床数据进行了非系统性审查,涉及西汀蛋白介导的免疫活性和西妥昔单抗的组合方法与其他免疫疗法,包括ICIS,SCCHN和CRC。实际上,西汀昔单抗在肿瘤内空间中介导ADCC活性,并引用适应性和先天细胞免疫力。然而,反应性机制可能导致免疫抑制反馈环。因此,对于将ICIS与西雷昔单抗组合用于治疗晚期肿瘤的强烈基本原理,因为靶向CTLA-4,PD-1和PD-L1可以表面上克服肿瘤微环境中的这些免疫抑制反应机制。此外,将ICIS(或其他免疫疗法)与西妥昔单抗组合是一种有望的策略,用于提高免疫应答和提高反应率和反应的耐久性。香条免疫活性 - 包括但不限于ADCC - 为其与ICIS或其他免疫检查组合提供了强烈的基本原理,以协同互动,并完全动员对肿瘤细胞的适应性和先天免疫力。正在进行的前瞻性研究将评估这些组合方案的临床效果及其在CRC和SCCHN中以及其他适应症中的免疫效应。

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