Abstract 1408: Intrahepatic IgA complex induces polarization of cancer-associated fibroblasts to matrix phenotypes in the tumor microenvironment of HCC

表型 肿瘤微环境 癌症研究 癌相关成纤维细胞 癌症 医学 生物 内科学 肿瘤细胞 遗传学 基因
作者
Shin Hee Yoon
出处
期刊:Cancer Research [American Association for Cancer Research]
卷期号:84 (6_Supplement): 1408-1408
标识
DOI:10.1158/1538-7445.am2024-1408
摘要

Abstract Background and Aims: Cancer-associated fibroblasts (CAFs) are activated fibroblasts that play key roles in the tumor microenvironment (TME). Immunoglobulin A (IgA) contributes to inflammation and anti-tumor immunity dismantling in the human liver. We investigated the effects of the IgA complex on CAFs in the TME of hepatocellular carcinoma (HCC). Approach and Results: CAF dynamics in HCC TME were analyzed via single-cell RNA sequencing of HCC samples. CAFs were isolated from 40 HCC samples. The isolated CAFs were treated with mock or serum-derived IgA dimers. Following treatment with the mock or serum IgA dimers in vitro, co-culture experiments were performed using CAF and CD8+ T cells. Single-cell analysis showed that sub-cluster proportions in the CAF-fibroblast activation protein-α (FAP) matrix were significantly increased in patients with high serum IgA levels. We were performed flow cytometry on fresh surgical tissues and observed a significant increase in the mean fluorescence intensity (MFI) of FAP in the CD68+ cells from patients with high serum IgA levels compared to those with low serum IgA levels (p<0.001). We validated that the transferrin receptor (CD71) is expressed in CAFs (p<0.01). IgA-treated CAFs exhibited higher programmed death-ligand 1 (PD-L1) expression levels than mock-treated CAFs (p<0.05). Co-culture with CAFs induced the attenuation of the cytotoxic function of activated CD8+ T cell, and these cells co-cultured with IgA-treated CAFs exhibited increased expression levels of programmed death-1 (PD-1) compared to those co-cultured with mock-treated CAFs (p<0.05). Conclusions: Intrahepatic IgA induces polarization of HCC CAFs into more malignant matrix phenotype and attenuates cytotoxic T cell function. Our study uncovers five dynamic CAF subpopulations within HCC tissues and highlights their potential roles in tumor progression and immune suppression. Citation Format: Pil Soo Sung. Intrahepatic IgA complex induces polarization of cancer-associated fibroblasts to matrix phenotypes in the tumor microenvironment of HCC [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2024; Part 1 (Regular Abstracts); 2024 Apr 5-10; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2024;84(6_Suppl):Abstract nr 1408.

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
meng发布了新的文献求助10
刚刚
zzz完成签到,获得积分10
1秒前
Yziii应助沸点采纳,获得20
3秒前
4秒前
4秒前
4秒前
体贴的忆曼完成签到,获得积分10
5秒前
5秒前
stefan完成签到,获得积分10
5秒前
iwhisper完成签到,获得积分10
6秒前
多亿点完成签到,获得积分10
6秒前
6秒前
7秒前
7秒前
7秒前
8秒前
wddfz发布了新的文献求助10
9秒前
9秒前
iwhisper发布了新的文献求助10
10秒前
666完成签到,获得积分20
10秒前
10秒前
典雅书翠完成签到,获得积分10
11秒前
sws发布了新的文献求助10
11秒前
搜集达人应助Aprial采纳,获得10
11秒前
共享精神应助lincsh采纳,获得10
11秒前
SciGPT应助谦让的樱采纳,获得10
11秒前
羽言发布了新的文献求助10
11秒前
姜一完成签到,获得积分10
12秒前
11完成签到,获得积分10
12秒前
鲤鱼梦柳完成签到 ,获得积分10
12秒前
高兴的巨人完成签到 ,获得积分10
12秒前
研友_Z1eDgZ发布了新的文献求助10
13秒前
666发布了新的文献求助10
13秒前
pluto应助犹豫的灵萱采纳,获得10
13秒前
不配.应助绝世镜天采纳,获得50
13秒前
蓝蜗牛完成签到,获得积分10
14秒前
FashionBoy应助wddfz采纳,获得10
15秒前
为溪完成签到,获得积分10
17秒前
红烧茄子完成签到,获得积分10
18秒前
Singularity应助happy杨采纳,获得10
19秒前
高分求助中
Sustainability in Tides Chemistry 2800
The Young builders of New china : the visit of the delegation of the WFDY to the Chinese People's Republic 1000
Rechtsphilosophie 1000
Bayesian Models of Cognition:Reverse Engineering the Mind 888
Le dégorgement réflexe des Acridiens 800
Defense against predation 800
Very-high-order BVD Schemes Using β-variable THINC Method 568
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3135752
求助须知:如何正确求助?哪些是违规求助? 2786595
关于积分的说明 7778521
捐赠科研通 2442742
什么是DOI,文献DOI怎么找? 1298676
科研通“疑难数据库(出版商)”最低求助积分说明 625205
版权声明 600866