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:Basic immunohistochemistry for lymphoma diagnosis.
免疫组织化学是一种利用抗原-抗体相互作用检测细胞中特定蛋白质的技术。
免疫组化是一种利用抗原-抗体相互作用检测细胞中特定蛋白质的技术。该技术在淋巴瘤诊断中有若干重要应用,包括识别细胞谱系和成熟阶段、检测特定遗传学改变、显示细胞增殖程度以及识别治疗靶点。CD3是一种泛T细胞标志物,除间变性大细胞淋巴瘤外,在大多数成熟T/NK细胞淋巴瘤中表达,而CD20是一种泛B细胞标志物,在大多数成熟B细胞淋巴瘤中表达。CD79a可能是CD20的良好替代标志物,可弥补因肿瘤细胞浆细胞样分化或既往利妥昔单抗使用史导致的CD20丢失。CD56是一种神经内分泌标志物,在淋巴瘤诊断中用作NK细胞标志物。滤泡性淋巴瘤(BCL2)和套细胞淋巴瘤(CCND1)中发生的特征性易位可分别通过免疫组化中Bcl-2和cyclin D-1的过表达来检测。Ki-67通过标记处于G0期以外细胞周期阶段的细胞来反映肿瘤细胞增殖程度。随着免疫治疗的发展,针对programmed death-ligand 1(PD-L1)、CD19和CD30等标志物的多种抗体已被用作生物标志物以识别治疗靶点。正确固定标本对于获得准确的免疫组化结果至关重要。因此,从组织采集到最终病理诊断的所有流程都必须适当进行,以实现准确的淋巴瘤诊断。
Immunohistochemistry is a technique that uses antigen-antibody interactions to detect specific proteins in cells. This technique has several essential applications in lymphoma diagnosis, including identifying the cell lineage and phase of maturation, detecting specific genetic alterations, visualizing the degree of cell proliferation, and identifying therapeutic targets. CD3 is a pan T-cell marker expressed on most of the mature T/NK-cell lymphomas, except for anaplastic large cell lymphoma, whereas CD20 is a pan B-cell marker that is expressed on most of the mature B-cell lymphomas. CD79a may be a good alternative to CD20, compensating for its loss owing to the plasmocytic differentiation of tumor cells or history of rituximab administration. CD56, a neuroendocrine marker, is used as an NK cell marker in lymphoma diagnosis. Characteristic translocations occurring in follicular lymphoma ( BCL2 ) and mantle cell lymphoma ( CCND1 ) can be detected by the overexpression of Bcl-2 and cyclin D-1 in immunohistochemistry, respectively. Ki-67 reflects the degree of tumor cell proliferation by indicating cells in cell cycle phases other than G0. With the development of immunotherapy, several antibodies against markers such as programmed death-ligand 1 (PD-L1), CD19, and CD30 have been used as biomarkers to identify therapeutic targets. It is critical to properly fix the specimens to obtain accurate immunohistochemical results. Therefore, all processes, from tissue collection to the final pathological diagnosis, must be performed appropriately for accurate lymphoma diagnosis.
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