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新型基于蛋白质的抗自身抗原疫苗可减少小鼠散发性结肠腺瘤的形成。

Novel Protein-Based Vaccine against Self-Antigen Reduces the Formation of Sporadic Colon Adenomas in Mice.

作者信息

Belnoue Elodie, Leystra Alyssa A, Carboni Susanna, Cooper Harry S, Macedo Rodrigo T, Harvey Kristen N, Colby Kimberly B, Campbell Kerry S, Vanderveer Lisa A, Clapper Margie L, Derouazi Madiha

机构信息

AMAL Therapeutics, Fondation pour Recherches Médicales, 64 avenue de la Roseraie, 1205 Geneva, Switzerland.

Boehringer Ingelheim International GmbH, 55216 Ingelheim, Germany.

出版信息

Cancers (Basel). 2021 Feb 17;13(4):845. doi: 10.3390/cancers13040845.

Abstract

Novel immunopreventive strategies are emerging that show great promise for conferring long-term protection to individuals at high risk of developing colorectal cancer. The KISIMA vaccine platform utilizes a chimeric protein comprising: (1) a selected tumor antigen; (2) a cell-penetrating peptide to improve antigen delivery and epitope presentation, and (3) a TLR2/4 agonist to serve as a self-adjuvant. This study examines the ability of a KISIMA vaccine against achaete-scute family bHLH transcription factor 2 (Ascl2), an early colon cancer antigen, to reduce colon tumor formation by stimulating an anti-tumor immune response. Vaccine administrations were well-tolerated and led to circulating antibodies and antigen-specific T cells in a mouse model of colorectal cancer. To assess preventive efficacy, the vaccine was administered to mice either alone or in combination with the immune checkpoint inhibitor anti-PD-1. When delivered to animals prior to colon tumor formation, the combination strategy significantly reduced the development of colon microadenomas and adenomas, as compared to vehicle-treated controls. This response was accompanied by an increase in the intraepithelial density of CD3+ T lymphocytes. Together, these data indicate that the KISIMA-Ascl2 vaccine shows great potential to be a safe and potent immunopreventive intervention for individuals at high risk of developing colorectal cancer.

摘要

新型免疫预防策略正在兴起,有望为罹患结直肠癌风险高的个体提供长期保护。KISIMA疫苗平台利用一种嵌合蛋白,该蛋白包含:(1)一种选定的肿瘤抗原;(2)一种细胞穿透肽以改善抗原递送和表位呈递,以及(3)一种TLR2/4激动剂作为自身佐剂。本研究考察了一种针对早期结肠癌抗原achaete-scute家族bHLH转录因子2(Ascl2)的KISIMA疫苗通过刺激抗肿瘤免疫反应来减少结肠肿瘤形成的能力。在结直肠癌小鼠模型中,疫苗给药耐受性良好,并导致循环抗体和抗原特异性T细胞产生。为评估预防效果,将疫苗单独或与免疫检查点抑制剂抗PD-1联合给予小鼠。当在结肠肿瘤形成前给予动物时,与载体处理的对照组相比,联合策略显著减少了结肠微腺瘤和腺瘤的发生。这种反应伴随着上皮内CD3+T淋巴细胞密度的增加。总之,这些数据表明,KISIMA-Ascl2疫苗对于罹患结直肠癌风险高的个体而言,具有成为一种安全有效的免疫预防干预措施的巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63c7/7923075/7de2625c389c/cancers-13-00845-g001.jpg

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