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:Characteristics of Peripheral Blood Lymphocyte Populations in Patients with Locally Advanced Unresectable Non-Small Cell Lung Cancer.
Characteristics of Peripheral Blood Lymphocyte Populations in Patients with Locally Advanced Unresectable Non-Small Cell Lung Cancer.
在局部晚期NSCLC(IIIB-IIIC期)患者中,免疫活性外周血细胞之间显现出的多向性变化,无疑可被视为该队列中系统性免疫紊乱(继发性免疫缺陷)的标志。
不可切除NSCLC的主要治疗类型是放化疗,其毒性相对较高。允许降低这种方法毒性的一种选择可能是免疫矫正治疗。这种治疗类型的指定应在患者免疫系统反应方面有依据。这证实了在初治NSCLC患者中验证全身免疫紊乱的重要性。
评估IIIB、IIIC期原发性NSCLC患者外周血免疫细胞群体的特征,并识别该队列中是否存在继发性免疫缺陷的迹象。
我们采用八色流式细胞术分析了80例IIIB-IIIC期NSCLC患者和40例健康对照者中CD45+细胞(淋巴细胞)内循环T细胞(CD3+、CD4+、CD8+)、B细胞(CD19+)、NK细胞(CD3-CD16+CD56+细胞)和NKT细胞(CD3+CD56+细胞)的频率。
在IIIB-IIIC期原发性NSCLC患者中,发现免疫活性血细胞内部发生变化。此外,研究揭示定量变化影响所有主要免疫活性细胞。发现CD4+ T细胞和B淋巴细胞比例下降,NK和NKT细胞数量增加。同时,发现双阳性CD4+CD8+ T细胞数量增加,以及B淋巴细胞中B1a(CD5+CD19+)细胞比例显著增加(定性紊乱)。
BACKGROUND: The main type of treatment of unresectable NSCLC is chemoradiotherapy, which has a relatively high toxicity. One option allowing to reduce the toxicity of this approach may be immunocorrective therapy. The appointment of this type of treatment should be warranted in terms of patient's immune system response. This confirms the importance of verifying systemic immune disorders in primary patients with NSCLC. GOAL: To assess the features of the population of immune cells in peripheral blood in patients with stage IIIB, IIIC primary NSCLC and to identify any signs of secondary immunodeficiency in this cohort. METHODS: We analyzed the frequencies of circulating T cells (CD3+, CD4+, CD8+), B-cells (CD19+), NK-cells (CD3-CD16+CD56+ cell), and NKT-cells (CD3+CD56+ cells) within CD45+ cells (lymphocytes) in 80 patients with stage IIIB-IIIC NSCLC, and in 40 healthy controls using eight-color flow cytometry. RESULTS: In patients with stages IIIB-IIIC primary NSCLC, changes within immunocompetent blood cells were found. Moreover, it was unveiled that quantitative changes affected all major immunocompetent cells. A decrease in the proportion of CD4+ T cells and B lymphocytes and an increase in the number of NK and NKT cells were found. Also, an increase in the number of double-positive CD4+CD8+ T cells was revealed, as well as a significant increase in the proportion of B1a (CD5+CD19+) cells among B lymphocytes (qualitative disorders). CONCLUSION: The revealed multidirectional changes among immunocompetent peripheral blood cells in patients with locally advanced NSCLC (stages IIIB-IIIC) can be beyond doubt considered as signs of systemic immune disorders in this cohort (secondary immunodeficiency).
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