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抗原呈递激活的 pDCs 在促进 Th17 细胞和影响抗肿瘤免疫中的新作用。

New role for antigen-presenting activated pDCs in promoting Th17 cells and impacting antitumor immunity.

机构信息

Department of Pathology and Immunology; University of Geneva Medical School ; Geneva, Switzerland.

出版信息

Oncoimmunology. 2015 May 8;4(5):e988476. doi: 10.4161/2162402X.2014.988476. eCollection 2015 May.

DOI:10.4161/2162402X.2014.988476
PMID:26155409
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4485838/
Abstract

Plasmacytoid dendritic cells (pDCs) are not only potent inflammatory cytokine producers but also function as antigen-presenting cells (APCs). We have shown that vaccination using CpG-B activated tumor antigen (Ag) presenting pDCs induce Th17 cells that promote intratumoral immune cell recruitment, including antitumor cytotoxic T lymphocytes CTLs. Therefore, strategies targeting both innate and adaptive pDC functions may improve antitumor T-cell immunity.

摘要

浆细胞样树突状细胞(pDCs)不仅是强有力的炎症细胞因子产生细胞,而且还作为抗原呈递细胞(APCs)发挥作用。我们已经表明,使用 CpG-B 激活的肿瘤抗原(Ag)呈递 pDC 进行疫苗接种可诱导 Th17 细胞,促进肿瘤内免疫细胞募集,包括抗肿瘤细胞毒性 T 淋巴细胞(CTLs)。因此,针对先天和适应性 pDC 功能的策略可能会改善抗肿瘤 T 细胞免疫。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22ec/4485838/7b58861c3952/koni-04-05-988476-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22ec/4485838/7b58861c3952/koni-04-05-988476-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/22ec/4485838/7b58861c3952/koni-04-05-988476-g001.jpg

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肿瘤细胞的膜转移克服了浆细胞样树突状细胞吞噬能力的缺陷,使其能够获取和呈递肿瘤抗原。
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Tumor promotion by intratumoral plasmacytoid dendritic cells is reversed by TLR7 ligand treatment.肿瘤内浆细胞样树突状细胞促进肿瘤发生可被 TLR7 配体治疗逆转。
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