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基于树突状细胞的免疫疗法的范式转变:从体外生成的单核细胞衍生树突状细胞到自然循环的树突状细胞亚群

Paradigm Shift in Dendritic Cell-Based Immunotherapy: From in vitro Generated Monocyte-Derived DCs to Naturally Circulating DC Subsets.

作者信息

Wimmers Florian, Schreibelt Gerty, Sköld Annette E, Figdor Carl G, De Vries I Jolanda M

机构信息

Department of Tumor Immunology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center , Nijmegen , Netherlands.

Department of Tumor Immunology, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center , Nijmegen , Netherlands ; Department of Medical Oncology, Radboud University Medical Center , Nijmegen , Netherlands.

出版信息

Front Immunol. 2014 Apr 11;5:165. doi: 10.3389/fimmu.2014.00165. eCollection 2014.

Abstract

Dendritic cell (DC)-based immunotherapy employs the patients' immune system to fight neoplastic lesions spread over the entire body. This makes it an important therapy option for patients suffering from metastatic melanoma, which is often resistant to chemotherapy. However, conventional cellular vaccination approaches, based on monocyte-derived DCs (moDCs), only achieved modest response rates despite continued optimization of various vaccination parameters. In addition, the generation of moDCs requires extensive ex vivo culturing conceivably hampering the immunogenicity of the vaccine. Recent studies, thus, focused on vaccines that make use of primary DCs. Though rare in the blood, these naturally circulating DCs can be readily isolated and activated thereby circumventing lengthy ex vivo culture periods. The first clinical trials not only showed increased survival rates but also the induction of diversified anti-cancer immune responses. Upcoming treatment paradigms aim to include several primary DC subsets in a single vaccine as pre-clinical studies identified synergistic effects between various antigen-presenting cells.

摘要

基于树突状细胞(DC)的免疫疗法利用患者的免疫系统来对抗遍布全身的肿瘤病变。这使其成为转移性黑色素瘤患者的重要治疗选择,转移性黑色素瘤通常对化疗耐药。然而,基于单核细胞衍生DC(moDC)的传统细胞疫苗接种方法,尽管不断优化各种疫苗接种参数,仅取得了适度的应答率。此外,moDC的生成需要大量的体外培养,这可能会妨碍疫苗的免疫原性。因此,最近的研究集中在利用原始DC的疫苗上。这些自然循环的DC虽然在血液中很少见,但可以很容易地分离和激活,从而避免了漫长的体外培养期。首批临床试验不仅显示出生存率提高,还诱导了多样化的抗癌免疫反应。由于临床前研究确定了各种抗原呈递细胞之间的协同作用,即将到来的治疗模式旨在将几种原始DC亚群纳入单一疫苗中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce26/3990057/ba20de96dc59/fimmu-05-00165-g001.jpg

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