不适合移植的大 B 细胞淋巴瘤二线使用 axicabtagene ciloleucel:ALYCANTE 最终分析
Second-line axicabtagene ciloleucel in large B-cell lymphoma ineligible for transplantation: ALYCANTE final analysis.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Qin Huang formula enhances the effect of Adriamycin in B-cell lymphoma via increasing tumor infiltrating lymphocytes by targeting toll-like receptor signaling pathway.
Qin Huang formula enhances the effect of Adriamycin in B-cell lymphoma via increasing tumor infiltrating lymphocytes by targeting toll-like receptor signaling pathway.
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QHF 联合 ADM 通过调节肿瘤免疫微环境增强 ADM 的抗肿瘤效果,可作为 B 细胞淋巴瘤患者的联合治疗策略。
作为原创中药方剂,芩黄方(QHF)在我院用作治疗淋巴瘤的辅助疗法,并已证实与化疗联合使用时具有疗效。然而,QHF的潜在机制尚未阐明。
采用基于网络药理学的分析方法筛选QHF治疗B细胞淋巴瘤的活性成分并预测其潜在机制。随后,建立小鼠模型以在体内验证QHF联合阿霉素(ADM)的抗肿瘤效果。最后,通过IHC、ELISA、18 F-FDG PET-CT扫描和western blot揭示QHF治疗B细胞淋巴瘤的潜在机制。
系统药理学研究揭示,QHF在人体内以多靶点、多途径模式发挥作用。体内研究表明,QHF与ADM联合治疗在同系小鼠模型中强效抑制B细胞淋巴瘤生长,并显著增加肿瘤微环境(TME)中肿瘤浸润CD4+和CD8+ T细胞的比例。此外,联合治疗组中CXCL10和IL-6水平显著升高。最后,western blot显示联合治疗组中TLR2和p38 MAPK水平升高。
As an original traditional Chinese medicinal formula, Qin Huang formula (QHF) is used as adjuvant therapy for treating lymphoma in our hospital and has proven efficacy when combined with chemotherapy. However, the underlying mechanisms of QHF have not been elucidated.
A network pharmacological-based analysis method was used to screen the active components and predict the potential mechanisms of QHF in treating B cell lymphoma. Then, a murine model was built to verify the antitumor effect of QHF combined with Adriamycin (ADM) in vivo. Finally, IHC, ELISA, 18 F-FDG PET-CT scan, and western blot were processed to reveal the intriguing mechanism of QHF in treating B cell lymphoma.
The systemic pharmacological study revealed that QHF took effect following a multiple-target and multiple-pathway pattern in the human body. In vivo study showed that combination therapy with QHF and ADM potently inhibited the growth of B cell lymphoma in a syngeneic murine model, and significantly increased the proportion of tumor infiltrating CD4+ and CD8+ T cells in the tumor microenvironment (TME). Furthermore, the level of CXCL10 and IL-6 was significantly increased in the combination group. Finally, the western blot exhibited that the level of TLR2 and p38 MAPK increased in the combination therapy group.
QHF in combination of ADM enhances the antitumor effect of ADM via modulating tumor immune microenvironment and can be a combination therapeutic strategy for B cell lymphoma patients.
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