决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Innate and Adaptive Immunity during SARS-CoV-2 Infection: Biomolecular Cellular Markers and Mechanisms.
2019冠状病毒病(COVID-19)大流行由正链单股RNA(ssRNA)严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起。
2019冠状病毒病(COVID-19)大流行由正链单股RNA(ssRNA)严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起。然而,其他人类冠状病毒(hCoVs)也存在。历史上的大流行包括天花和流感,通过有效靶向具有能力的宿主免疫系统反应,利用有效的治疗手段来减少总体疾病负担。免疫系统由初级/次级淋巴结构组成,最初有八种免疫细胞类型,以及许多其他亚型,它们利用细胞信号级联穿越细胞膜,有助于清除病原蛋白。讨论的其他蛋白包括分化簇(CD)标志物、主要组织相容性复合体(MHC)、多效性白细胞介素(IL)和趋化因子(CXC)。宿主免疫的历史概念是固有免疫和适应性免疫系统。适应性免疫系统由T细胞、B细胞和抗体代表。固有免疫系统由巨噬细胞、中性粒细胞、树突状细胞和补体系统代表。其他病毒可以影响和调节细胞周期进程,例如,在包括人乳头瘤病毒(HPV:宫颈癌)、EB病毒(EBV:淋巴瘤)、乙型和丙型肝炎(HB/HC:肝细胞癌)以及人类T细胞白血病病毒-1(T细胞白血病)在内的癌症中。细菌感染也会增加患癌症的风险(例如,幽门螺杆菌)。病毒和细菌因素可以通过影响宿主免疫反应,在临床和社区环境中传播的同时,导致发病和死亡。因此,将单细胞测序的进展与其他实验室技术相结合,以深入了解免疫细胞特征,是恰当的做法。这些发展提供了更清晰的认识和理解,与可能受固有B细胞(B1+或边缘区细胞)或针对SARS-CoV-2感染及其他病理的适应性T细胞反应影响的自身免疫状况相重叠。因此,本综述首先介绍宿主呼吸道感染,然后探讨宝贵的细胞信使蛋白,最后讨论个体免疫细胞标志物。
The coronavirus 2019 (COVID-19) pandemic was caused by a positive sense single-stranded RNA (ssRNA) severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). However, other human coronaviruses (hCoVs) exist. Historical pandemics include smallpox and influenza, with efficacious therapeutics utilized to reduce overall disease burden through effectively targeting a competent host immune system response. The immune system is composed of primary/secondary lymphoid structures with initially eight types of immune cell types, and many other subtypes, traversing cell membranes utilizing cell signaling cascades that contribute towards clearance of pathogenic proteins. Other proteins discussed include cluster of differentiation (CD) markers, major histocompatibility complexes (MHC), pleiotropic interleukins (IL), and chemokines (CXC). The historical concepts of host immunity are the innate and adaptive immune systems. The adaptive immune system is represented by T cells, B cells, and antibodies. The innate immune system is represented by macrophages, neutrophils, dendritic cells, and the complement system. Other viruses can affect and regulate cell cycle progression for example, in cancers that include human papillomavirus (HPV: cervical carcinoma), Epstein-Barr virus (EBV: lymphoma), Hepatitis B and C (HB/HC: hepatocellular carcinoma) and human T cell Leukemia Virus-1 (T cell leukemia). Bacterial infections also increase the risk of developing cancer (e.g., Helicobacter pylori ). Viral and bacterial factors can cause both morbidity and mortality alongside being transmitted within clinical and community settings through affecting a host immune response. Therefore, it is appropriate to contextualize advances in single cell sequencing in conjunction with other laboratory techniques allowing insights into immune cell characterization. These developments offer improved clarity and understanding that overlap with autoimmune conditions that could be affected by innate B cells (B1 + or marginal zone cells) or adaptive T cell responses to SARS-CoV-2 infection and other pathologies. Thus, this review starts with an introduction into host respiratory infection before examining invaluable cellular messenger proteins and then individual immune cell markers.
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