RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:CD29 targeted near-infrared photoimmunotherapy (NIR-PIT) in the treatment of a pigmented melanoma model.
CD29 targeted near-infrared photoimmunotherapy (NIR-PIT) in the treatment of a pigmented melanoma model.
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近红外光免疫疗法(NIR-PIT)是一种新开发的癌症治疗方法,利用抗体-光吸收剂偶联物(AbPC)结合NIR光。注射AbPC后,其与肿瘤结合,随后NIR光照射引起光化学反应,选择性杀死癌细胞。NIR-PIT是治疗位于体表的皮肤癌(如黑色素瘤)的理想方法。
然而,有人担心黑色素瘤病灶中的色素可能干扰光的传递,使治疗无效。我们在高度色素沉着的B16黑色素瘤模型中研究了靶向CD29和CD44的NIR-PIT(分别为CD29-PIT和CD44-PIT)的疗效。虽然CD29-PIT和CD44-PIT在体外和体内均能杀死B16细胞,但CD29-PIT更有效地抑制了肿瘤生长。Ki67表达显示,CD29-PIT后存活的细胞增殖能力较低,表明CD29-PIT对增殖更活跃的癌细胞具有选择性。CD29-PIT不杀死免疫细胞,而CD44-PIT则杀死T细胞和NK细胞以及大多数髓系细胞,包括DCs,这可能干扰对NIR-PIT的免疫应答。在CD29-PIT中加入抗CTLA4抗体免疫检查点抑制剂(ICI)增加了CD8 T细胞的浸润,增强了肿瘤抑制并延长了生存期。当抗CTLA4 ICI与CD44-PIT联合使用时,这些效果不太明显。CD29-PIT后肿瘤微环境(TME)中免疫细胞的保留可能导致了与抗CTLA4治疗联合时更好的应答。
我们得出结论,NIR-PIT可用于色素性黑色素瘤,且CD29是NIR-PIT的一个有前景的靶点,适合与其他免疫疗法联合治疗。
Near-infrared photoimmunotherapy (NIR-PIT) is a newly developed cancer treatment that utilizes an antibody-photoabsorber-conjugate (AbPC) combined with NIR light. The AbPC is injected and binds to the tumor whereupon NIR light irradiation causes a photochemical reaction that selectively kills cancer cells. NIR-PIT is ideal for surface-located skin cancers such as melanoma.
However, there is concern that the pigment in melanoma lesions could interfere with light delivery, rendering treatment ineffective.
We investigated the efficacy of CD29- and CD44-targeted NIR-PIT (CD29-PIT and CD44-PIT, respectively) in the B16 melanoma model, which is highly pigmented. While CD29-PIT and CD44-PIT killed B16 cells in vitro and in vivo , CD29-PIT suppressed tumor growth more efficiently. Ki67 expression showed that cells surviving CD29-PIT were less proliferative, suggesting that CD29-PIT was selective for more proliferative cancer cells.
CD29-PIT did not kill immune cells, whereas CD44-PIT killed both T and NK cells and most myeloid cells, including DCs, which could interfere with the immune response to NIR-PIT. The addition of anti-CTLA4 antibody immune checkpoint inhibitor (ICI) to CD29-PIT increased the infiltration of CD8 T cells and enhanced tumor suppression with prolonged survival.
Such effects were less prominent when the anti-CTLA4 ICI was combined with CD44-PIT. The preservation of immune cells in the tumor microenvironment (TME) after CD29-PIT likely led to a better response when combined with anti-CTLA4 treatment.
We conclude that NIR-PIT can be performed in pigmented melanomas and that CD29 is a promising target for NIR-PIT, which is amenable to combination therapy with other immunotherapies.
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