为肝细胞癌武装 GPC3 CAR-T 细胞:多少才足够,下一步是什么?
Armouring GPC3 CAR T cells for hepatocellular carcinoma: how much is enough and what comes next?
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Luteolin exerts anti-tumour immunity in hepatocellular carcinoma by accelerating CD8(+) T lymphocyte infiltration.
Luteolin exerts anti-tumour immunity in hepatocellular carcinoma by accelerating CD8(+) T lymphocyte infiltration.
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木犀草素是一种常用的中药,几十年来一直用于肝细胞癌(HCC)的治疗。既往研究已证实其抗肿瘤疗效,但其潜在机制仍不清楚。本研究旨在评估木犀草素对H22荷瘤小鼠的治疗效果。木犀草素在成熟的HCC小鼠模型中有效抑制了实体瘤的生长。高通量测序显示,木犀草素治疗可增强T细胞活化、细胞趋化性和细胞因子产生。此外,木犀草素有助于维持脾脏、外周血和肿瘤组织中CD8 + T淋巴细胞的高比例。本研究还探讨了木犀草素对肿瘤浸润CD8 + T淋巴细胞表型和功能变化的影响。木犀草素恢复了H22荷瘤小鼠肿瘤浸润CD8 + T淋巴细胞的细胞毒性。CD8 + T淋巴细胞表现出增强的表型活化,血清中颗粒酶B、IFN-γ和TNF-α的产生增加。木犀草素与PD-1抑制剂联合给药增强了H22荷瘤小鼠的抗肿瘤效果。木犀草素可通过诱导CD8 + T淋巴细胞浸润发挥抗肿瘤免疫反应,并增强PD-1抑制剂对H22荷瘤小鼠的抗肿瘤效果。
Luteolin, a commonly used traditional Chinese medicine, has been utilized for several decades in the treatment of hepatocellular carcinoma (HCC). Previous research has demonstrated its anti-tumour efficacy, but its underlying mechanism remains unclear.
This study aimed to assess the therapeutic effects of luteolin in H22 tumour-bearing mice. luteolin effectively inhibited the growth of solid tumours in a well-established mouse model of HCC. High-throughput sequencing revealed that luteolin treatment could enhance T-cell activation, cell chemotaxis and cytokine production.
In addition, luteolin helped sustain a high ratio of CD8 + T lymphocytes in the spleen, peripheral blood and tumour tissues. The effects of luteolin on the phenotypic and functional changes in tumour-infiltrating CD8 + T lymphocytes were also investigated. Luteolin restored the cytotoxicity of tumour-infiltrating CD8 + T lymphocytes in H22 tumour-bearing mice.
The CD8 + T lymphocytes exhibited intensified phenotype activation and increased production of granzyme B, IFN-γ and TNF-α in serum. The combined administration of luteolin and the PD-1 inhibitor enhanced the anti-tumour effects in H22 tumour-bearing mice. Luteolin could exert an anti-tumour immune response by inducing CD8 + T lymphocyte infiltration and enhance the anti-tumour effects of the PD-1 inhibitor on H22 tumour-bearing mice.
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