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CD29 靶向近红外光免疫疗法(NIR-PIT)在色素性黑色素瘤模型治疗中的应用

英文原题:CD29 targeted near-infrared photoimmunotherapy (NIR-PIT) in the treatment of a pigmented melanoma model.

查看英文原题

CD29 targeted near-infrared photoimmunotherapy (NIR-PIT) in the treatment of a pigmented melanoma model.

PubMed 2022/01/04(内容时间) Oncoimmunology Q1 · IF 6.2(JCR 2025)

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中文摘要

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。

展开英文摘要原文

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.

论文信息

作者
Furusawa A、Okada R、Inagaki F、Wakiyama H、Kato T、Furumoto H、Fukushima H、Okuyama S
单位
Molecular Imaging Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, USA.United States
文献类型
美国 NIH 院内研究
期刊
Oncoimmunology2022
原文标识
PubMed 35003897 · DOI 10.1080/2162402X.2021.2019922