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用一种α 型 1 极化树突状细胞疫苗靶向周细胞抗原 DLK1 可导致肿瘤血管调节和防止结肠癌进展。

Targeting the pericyte antigen DLK1 with an alpha type-1 polarized dendritic cell vaccine results in tumor vascular modulation and protection against colon cancer progression.

机构信息

Department of Immunotherapeutics and Biotechnology, Jerry H. Hodge School of Pharmacy, Texas Tech University Health Sciences Center, Abilene, TX, United States.

Department of Public Health, School of Population and Public Health, Texas Tech University Health Sciences Center, Lubbock, TX, United States.

出版信息

Front Immunol. 2023 Oct 2;14:1241949. doi: 10.3389/fimmu.2023.1241949. eCollection 2023.

Abstract

Despite the availability of various treatment options, colorectal cancer (CRC) remains a significant contributor to cancer-related mortality. Current standard-of-care interventions, including surgery, chemotherapy, and targeted agents like immune checkpoint blockade and anti-angiogenic therapies, have improved short-term patient outcomes depending on disease stage, but survival rates with metastasis remain low. A promising strategy to enhance the clinical experience with CRC involves the use of dendritic cell (DC) vaccines that incite immunity against tumor-derived blood vessels, which are necessary for CRC growth and progression. In this report, we target tumor-derived pericytes expressing DLK1 with a clinically-relevant alpha type-1 polarized DC vaccine (αDC1) in a syngeneic mouse model of colorectal cancer. Our pre-clinical data demonstrate the αDC1 vaccine's ability to induce anti-tumor effects by facilitating cytotoxic T lymphocyte activity and ablating the tumor vasculature. This work, overall, provides a foundation to further interrogate immune-mediated mechanisms of protection in order to help devise efficacious αDC1-based strategies for patients with CRC.

摘要

尽管有多种治疗选择,但结直肠癌(CRC)仍然是癌症相关死亡的主要原因。目前的标准治疗干预措施,包括手术、化疗和靶向药物如免疫检查点阻断和抗血管生成疗法,根据疾病阶段改善了短期患者预后,但转移性生存率仍然较低。一种有前途的增强 CRC 临床体验的策略涉及使用树突状细胞(DC)疫苗,该疫苗引发针对肿瘤来源血管的免疫反应,这些血管对于 CRC 的生长和进展是必要的。在本报告中,我们针对结直肠癌细胞中表达 DLK1 的肿瘤衍生周细胞,使用一种临床相关的α1 型极化 DC 疫苗(αDC1)在结直肠癌细胞的同基因小鼠模型中进行靶向治疗。我们的临床前数据表明,αDC1 疫苗通过促进细胞毒性 T 淋巴细胞活性和消融肿瘤血管来诱导抗肿瘤作用。总的来说,这项工作为进一步研究免疫介导的保护机制提供了基础,以帮助制定针对 CRC 患者的有效基于αDC1 的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/613b/10578441/5f4ca50a2645/fimmu-14-1241949-g001.jpg

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