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一种结构简单的候选疫苗可减少三阴性乳腺癌的进展和扩散。

A Structurally Simple Vaccine Candidate Reduces Progression and Dissemination of Triple-Negative Breast Cancer.

作者信息

Amedei Amedeo, Asadzadeh Fatemeh, Papi Francesco, Vannucchi Maria Giuliana, Ferrucci Veronica, Bermejo Iris A, Fragai Marco, De Almeida Carolina Vieira, Cerofolini Linda, Giuntini Stefano, Bombaci Mauro, Pesce Elisa, Niccolai Elena, Natali Francesca, Guarini Eleonora, Gabel Frank, Traini Chiara, Catarinicchia Stefano, Ricci Federica, Orzalesi Lorenzo, Berti Francesco, Corzana Francisco, Zollo Massimo, Grifantini Renata, Nativi Cristina

机构信息

Department of Experimental and Clinical Medicine, University of Florence, Largo Brambilla 03, 50134 Firenze, Italy.

Department of Molecular Medicine and Medical Biotechnologies, University of Napoli "Federico II", via Pansini, 5, 80131 Napoli, Italy; CEINGE Biotecnologie Avanzata, Via Gaetano Salvatore 486, 80145 Napoli, Italy.

出版信息

iScience. 2020 Jun 26;23(6):101250. doi: 10.1016/j.isci.2020.101250. Epub 2020 Jun 6.

Abstract

The Tn antigen is a well-known tumor-associated carbohydrate determinant, often incorporated in glycopeptides to develop cancer vaccines. Herein, four copies of a conformationally constrained mimetic of the antigen TnThr (GalNAc-Thr) were conjugated to the adjuvant CRM197, a protein licensed for human use. The resulting vaccine candidate, mime[4]CRM elicited a robust immune response in a triple-negative breast cancer mouse model, correlated with high frequency of CD4+ T cells and low frequency of M2-type macrophages, which reduces tumor progression and lung metastasis growth. Mime[4]CRM-mediated activation of human dendritic cells is reported, and the proliferation of mime[4]CRM-specific T cells, in cancer tissue and peripheral blood of patients with breast cancer, is demonstrated. The locked conformation of the TnThr mimetic and a proper presentation on the surface of CRM197 may explain the binding of the conjugate to the anti-Tn antibody Tn218 and its efficacy to fight cancer cells in mice.

摘要

Tn抗原是一种著名的肿瘤相关碳水化合物决定簇,常被整合到糖肽中以开发癌症疫苗。在此,将四个拷贝的抗原TnThr(N-乙酰半乳糖胺-苏氨酸)的构象受限模拟物与佐剂CRM197偶联,CRM197是一种获许用于人类的蛋白质。所得候选疫苗mime[4]CRM在三阴性乳腺癌小鼠模型中引发了强烈的免疫反应,这与CD4+T细胞的高频率和M2型巨噬细胞的低频率相关,从而减少了肿瘤进展和肺转移生长。报道了mime[4]CRM介导的人树突状细胞激活,并证明了在乳腺癌患者的癌组织和外周血中mime[4]CRM特异性T细胞的增殖。TnThr模拟物的锁定构象以及在CRM197表面的适当呈现可能解释了该偶联物与抗Tn抗体Tn218的结合及其在小鼠中对抗癌细胞的功效。

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