Emerging Paradigm-Shifting in Cancer Immunotherapeutic Towards Personalized Cancer Medicine and Potential Challenges

B. Sharma
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Abstract

Recently invented several cancer immunotherapies that have succeeded with a diversity of new agents for clinical use. As such, notable progress immensely facilitated the designing of numerous effective immunotherapeutic regimens. Therapeutic vaccines and immune checkpoint blockade have lately demonstrated an enormous therapeutic efficacy thus generated great excitement for the development of new avenues on cancer treatments. Immunotherapies are highly potential to generate tumor-specific responses, as well as maintaining long-lasting remissions, unraveling vital approaches for future discoveries of cancer medicine. Next-generation cancer immunotherapies engaged with native mono-bi-specific antibodies are intended to target at innate immune checkpoints, conditional designing activated immune stimulator, redirecting Innate Cell Engagers (ICEs). Similarly, Natural killer cells are engineered for multi-specific immune targeting utilizing adaptable affinities and avidities, redirecting innate immune cells (dendritic, macrophages & NK cells). Oncolytic adenovirus-mediated targeting to alter cold tumors into hot including challenging tumor heterogeneity via interfering tumor sub-clonality are attractive projections to develop several novels immune-oncologic therapeutics towards personalized cancer medicine.
癌症免疫治疗向个性化癌症医学的新范式转变及其潜在挑战
最近发明了几种癌症免疫疗法,并成功地开发了多种新的药物用于临床。因此,显著的进展极大地促进了许多有效免疫治疗方案的设计。治疗性疫苗和免疫检查点阻断最近显示出巨大的治疗效果,因此为癌症治疗新途径的开发带来了巨大的兴奋。免疫疗法极有可能产生肿瘤特异性反应,并保持长期缓解,为癌症医学的未来发现揭示重要方法。下一代癌症免疫疗法与天然单双特异性抗体相结合,旨在靶向先天免疫检查点,有条件地设计激活的免疫刺激物,重定向先天细胞参与物(ICEs)。类似地,自然杀伤细胞被设计用于利用适应性亲和力和亲和力的多特异性免疫靶向,重定向先天免疫细胞(树突状细胞、巨噬细胞和NK细胞)。溶瘤腺病毒介导的靶向将冷肿瘤变为热肿瘤,包括通过干扰肿瘤亚克隆性挑战肿瘤异质性,是开发几种针对个性化癌症药物的新型免疫肿瘤疗法的有吸引力的预测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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