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Coley's immunotherapy revived: Innate immunity as a link in priming cancer cells for an attack by adaptive immunity

机译:Coley的免疫疗法复苏:先天免疫作为引发癌细胞的链接,通过自适应免疫力攻击

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ABSTRACT: There is no doubt that immunotherapy lies in the spotlight of current cancer research and clinical trials. However, there are still limitations in the treatment response in certain types of tumors largely due to the presence of the complex network of immunomodulatory and immunosuppressive pathways. These limitations are not likely to be overcome by current immunotherapeutic options, which often target isolated steps in immune pathways preferentially involved in adaptive immunity. Recently, we have developed an innovative anti-cancer immunotherapeutic strategy that initially elicits a strong innate immune response with subsequent activation of adaptive immunity in mouse models. Robust primary innate immune response against tumor cells is induced by toll-like receptor ligands and anti-CD40 agonistic antibodies combined with the phagocytosis-stimulating ligand mannan, anchored to a tumor cell membrane by biocompatible anchor for membrane. This immunotherapeutic approach results in a dramatic therapeutic response in large established murine subcutaneous tumors including melanoma, sarcoma, pancreatic adenocarcinoma, and pheochromocytoma. Additionally, eradication of metastases and/or long-lasting resistance to subsequent re-challenge with tumor cells was also accomplished. Current and future advantages of this immunotherapeutic approach and its possible combinations with other available therapies are discussed in this review. ? 2019
机译:摘要:毫无疑问,免疫疗法在于目前癌症研究和临床试验的聚焦。然而,在某些类型的肿瘤中仍然存在于某些类型的肿瘤中的局限性,这主要是由于免疫调节和免疫抑制途径的复杂网络存在。目前的免疫治疗选择不太可能克服这些限制,这通常靶向优先参与适应性免疫的免疫途径中的孤立步骤。最近,我们开发了一种创新的抗癌免疫治疗策略,最初引发了强烈的先天免疫应答,随后在小鼠模型中激活自适应免疫。通过Toll样受体配体和抗CD40激动抗体诱导对肿瘤细胞的鲁棒初级先天免疫应答,所述抗CD40激动抗体与吞噬症刺激配体甘露体团,通过生物相容性锚定锚定向肿瘤细胞膜进行膜。这种免疫治疗方法导致大型已建立的鼠皮下肿瘤的戏剧性反应,包括黑素瘤,肉瘤,胰腺腺癌和嗜铬细胞瘤。另外,还完成了消除转移和/或长期抗肿瘤细胞随后重新攻击的抗性。本次审查中讨论了这种免疫治疗方法的当前和未来优势及其与其他可用疗法的可能组合。还2019年

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