生物血浆对癌症和其他可怕疾病的免疫调节作用

Q1 Medicine
Nagendra Kumar Kaushik * , Neha Kaushik , Manish Adhikari , Su-Jae Lee , Eun Ha Choi
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引用次数: 0

摘要

近年来,人们积极探索等离子体医学技术的应用。最近,非热等离子体作为一种安全的抗癌治疗方法已被证明具有潜力,可以杀死多种类型的癌症靶点[1-4]。目前迫切需要一种新的基于免疫调节的抗癌人类保健技术。我们研究的主要目标是通过诱导免疫调节来提高血浆对癌细胞和肿瘤微环境的疗效和选择性。对冷等离子体与免疫细胞和肿瘤微环境相互作用的基本认识有助于阐明等离子体诱导免疫刺激的基本机制。最近的初步研究表明,血浆可显著调节免疫细胞,并可诱导共培养条件下的癌细胞死亡[5-7]。在我们最近的一项研究中,我们使用单核细胞模型,我们发现冷血浆激活单核细胞向巨噬细胞样表型的分化,并可以增加线粒体/溶酶体的数量,这表明血浆可能刺激巨噬细胞的分化或激活。反过来,血浆活化的巨噬细胞的相互作用减少了致瘤性特征,如上皮-间质-转化(EMT)和肿瘤细胞的干细胞样群体。此外,血浆靶向巨噬细胞活性,从而通过TNF-α/NOS+ m1样表型的表达增强细胞凋亡。在另一项研究中,我们在皮肤和口腔癌模型中评估了血浆诱导损伤相关分子模式/免疫原性细胞死亡在免疫激活和癌症治疗中的作用。我们还启动了血浆诱导免疫调节治疗特应性皮炎皮肤病的研究。目前的研究工作主要包括血浆诱导免疫细胞活化;它们被用于治疗各种耐药肿瘤和其他可怕的疾病。我们的主要目标是:(i)阐明血浆诱导免疫调节的基本机制(ii)开发基于免疫调节的策略来治疗包括癌症在内的各种可怕疾病(iii)在临床前研究的基础上开展临床试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immuno-modulatory effect of bio-plasma against cancer and other dreadful disease

The application of plasma medicine technology has been actively explored over last several years. Recently, non-thermal plasma has demonstrated potential as a safe anticancer therapeutic approach that can kill various types of cancer targets [1-4]. There is the urgent need of new human health care’s technology against cancers based on immuno-modulations. Main target of our study is to enhance efficacy and selectivity of plasma on cancer cells and cancer microenvironment by inducing immune-modulations. Fundamental insights on the cold plasma interactions with the immune cells and cancer micro-environment can clarify the basic mechanisms of plasma induced immune-stimulation. Recent preliminary study suggests that plasma significantly modulated immune cells and can induce cancer cell death in co-culture condition [5-7]. In one of our recent studies, using a monocyte cell model, we show that cold plasma activates the differentiation of monocytes into a macrophage-like phenotype and can increase mitochondrial/lysosomal numbers, suggesting that plasma may stimulate macrophage differentiation or activation. In turn, the interaction of plasma-activated macrophage cells reduced pro-tumorigenic features such as epithelial-mesenchymal-transition (EMT) and the stem-like population of tumor cells. Furthermore, plasma targeted macrophage activity and consequently enhanced apoptosis via expression of the TNF-α/NOS+ M1-like phenotype. In another study we have evaluated role of plasma induced damage associated molecular patterns/ immunogenic cell death in immune activation and cancer treatment in skin and oral cancer models. We have also initiated a study on plasma induced immuno-modulations for treatment of atopic dermatitis skin disorder. Present research work mainly comprises plasma induced activation of immune cells; which find applications for curing various kinds of resistant tumors and other dreadful diseases. Our main objectives are (i) to clarify basic mechanism on plasma induced immuno-modulations (ii) to develop immunomodulation based strategy for the treatment of various dreadful diseases including cancers (iii) to initiate clinical trial based on pre-clinical study.

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来源期刊
Clinical Plasma Medicine
Clinical Plasma Medicine MEDICINE, RESEARCH & EXPERIMENTAL-
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