免疫检查点阻断通过扩增效应 CD8⁺ T 细胞克隆增强淋巴细胞清除性化疗诱导的抗肿瘤免疫
Immune Checkpoint Blockade Augments Lymphodepleting Chemotherapy-Induced Antitumor Immunity by Expanding Effector CD8+ T-cell Clones.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:An innovative cellular medicine approach via the utilization of novel nanotechnology-based biomechatronic platforms as a label-free biomarker for early melanoma diagnosis.
An innovative cellular medicine approach via the utilization of novel nanotechnology-based biomechatronic platforms as a label-free biomarker for early melanoma diagnosis.
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创新细胞医学(ICM)是快速发展的领域,有望用于治疗多种复杂且普遍存在的危及生命疾病,如多发性硬化症、关节炎、帕金森病、阿尔茨海默病、心脏病和癌症。结合纳米技术和生物机电学的进展,ICM从单细胞层面理解疾病本质,推动细胞疗法变革。本文聚焦癌症的复杂性,指出需要跨学科合作对其进行充分表征,以实现现代医学在细胞层面早期发现疾病、并可能阻断其增殖机制的目标。这也体现了作者在实验生物学与工程学交叉领域推进细胞医学的研究背景。为此,研究设计、建模、纳米制造并测试了两种新型微型化、高度多功能的生物机电平台,配有专用操作软件和微电子器件,并通过多项体外实验,研究并验证癌变机制假说:将细胞收缩力、膜电位和细胞形态关联起来,用于黑色素瘤癌细胞的早期检测和表征。
本研究的创新点有六项:(1)开发利用Heaviside阶跃函数及销钉力模型计算活细胞收缩力的数学模型;(2)基于拉普拉斯变换、傅里叶变换及其逆变换,并考虑Warburg扩散阻抗因子,推导细胞膜电位表达式;(3)纳米制造新型生物机电平台及配套微电子和定制软件,用于提取细胞物理和力学特性;(4)开发无标记生物标志物;(5)提出并证明将癌细胞力学生物学与生物物理学特性及疾病分期相关联的数学表达;(6)据作者所知,首次基于细胞膜电位及相关收缩力区分黑色素瘤癌细胞不同阶段和形态。这些成果可能为细胞治疗、临床前癌症早期诊断及免疫治疗药物开发带来新方向。未来可扩展所提出的技术平台,研究神经系统电化学信号在癌症形成中的作用,从而推动现代肿瘤学发展并探索靶向免疫治疗。
本研究还为免疫治疗实践者提供了平台,用于进一步研究细胞生物物理学如何抑制神经-癌症相互作用,并通过实验室基因工程改进FDA批准的CAR-T 细胞受体,使其更好地捕获癌症抗原。
该研究强调神经递质和电化学信号分子对塑造T细胞免疫功能及其阻止癌细胞增殖能力的重要作用。
Innovative cellular medicine (ICM) is an exponentially emerging field with a promising approach to combating complex and ubiquitous life-threatening diseases such as multiple sclerosis (MS), arthritis, Parkinson's disease, Alzheimer's, heart disease, and cancer.
Together with the advancement of nanotechnology and bio-mechatronics, ICM revolutionizes cellular therapy in understanding the essence and nature of the disease initiated at a single-cell level.
This paper focuses on the intricate nature of cancer that requires multi-disciplinary efforts to characterize it well in order to achieve the objectives of modern world contemporary medicine in the early detection of the disease at a cellular level and potentially arrest its proliferation mechanism. This justifies the multidisciplinary research backgrounds of the authors of this paper in advancing cellular medicine by bridging the gap between experimental biology and the engineering field.
Thus, in pursuing this approach, two novel miniaturized and highly versatile biomechatronic platforms with dedicated operating software and microelectronics are designed, modeled, nanofabricated, and tested in numerous in vitro experiments to investigate a hypothesis and arrive at a proven theorem in carcinogenesis by interrelating cellular contractile force, membrane potential, and cellular morphology for early detection and characterization of melanoma cancer cells. The novelties that flourished within this work are manifested in sixfold: (1) developing a mathematical model that utilizes a Heaviside step function, as well as a pin-force model to compute the contractile force of a living cell, (2) deriving an expression of cell-membrane potential based on Laplace and Fourier Transform and their Inverse Transform functions by encountering Warburg diffusion impedance factor, (3) nano-fabricating novel biomechatronic platforms with associated microelectronics and customized software that extract cellular physics and mechanics, (4) developing a label-free biomarker, (5) arrive at a proved theorem in developing a mathematical expression in relating cancer cell mechanobiology to its biophysics in connection to the stage of the disease, and (6) to the first time in literature, and to the best of the authors' knowledge, discriminating different stages and morphology of cancer cell melanoma based on their cell-membrane potentials, and associated contractile forces that could introduce a new venue of cellular therapeutic modalities, preclinical early cancer diagnosis, and a novel approach in immunotherapy drug development.
The proposed innovative technology-based versatile bio-mechatronic platforms shall be extended for future studies, investigating the role of electrochemical signaling of the nervous system in cancer formation that will significantly impact modern oncology by pursuing a targeted immunotherapy approach.
This work also provides a robust platform for immunotherapy practitioners in extending the study of cellular biophysics in stalling neural-cancer interactions, of which the FDA-approved chimeric antigen receptor (CAR)-T cell therapies can be enhanced (genetically engineered) in a lab by improving its receptors to capture cancer antigens.
This work amplifies the importance of studying neurotransmitters and electrochemical signaling molecules in shaping the immune T-cell function and its effectiveness in arresting cancer proliferation rate (mechanobiology mechanism).
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