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酰胺键连接的 C4′-糖基化修饰 KR N7000 可强烈刺激人不变自然杀伤 T 细胞并在人源化小鼠模型中发挥抗肿瘤免疫作用。

Amide-Linked C4″-Saccharide Modification of KRN7000 Provides Potent Stimulation of Human Invariant NKT Cells and Anti-Tumor Immunity in a Humanized Mouse Model.

机构信息

Department of Chemistry, The University of Connecticut, Storrs, Connecticut 06269-3060, United States.

Millennium Institute on Immunology and Immunotherapy, Programa de Inmunología, Instituto de Ciencias Biomédicas, Facultad de Medicina, Universidad de Chile, Santiago 8380453, Chile.

出版信息

ACS Chem Biol. 2020 Dec 18;15(12):3176-3186. doi: 10.1021/acschembio.0c00707. Epub 2020 Dec 9.

Abstract

Activation of invariant natural killer T (iNKT) cells by α-galactosylceramides (α-GalCers) stimulates strong immune responses and potent anti-tumor immunity. Numerous modifications of the glycolipid structure have been assessed to derive activating ligands for these T cells with altered and potentially advantageous properties in the induction of immune responses. Here, we synthesized variants of the prototypical α-GalCer, KRN7000, with amide-linked phenyl alkane substitutions on the C4″-position of the galactose ring. We show that these variants have weak iNKT cell stimulating activity in mouse models but substantially greater activity for human iNKT cells. The most active of the C4″-amides in our study showed strong anti-tumor effects in a partially humanized mouse model for iNKT cell responses. analysis suggested that the tether length and degree of flexibility of the amide substituent affected the recognition by iNKT cell antigen receptors of the C4″-amide substituted glycolipids in complex with their antigen presenting molecule CD1d. Our findings establish the use of stable C4″-amide linked additions to the sugar moiety for further exploration of the immunological effects of structural modifications of iNKT cell activating glycolipids and highlight the critical need for more accurate animal models to assess these compounds for immunotherapeutic potential in humans.

摘要

α-半乳糖神经酰胺(α-GalCer)激活不变自然杀伤 T(iNKT)细胞可刺激强烈的免疫反应和有效的抗肿瘤免疫。已经评估了糖脂结构的许多修饰,以衍生出具有改变的和潜在有利的特性的激活配体,用于诱导这些 T 细胞的免疫反应。在这里,我们合成了原型α-GalCer KRN7000 的变体,在半乳糖环的 C4″-位置上具有酰胺连接的苯烷取代基。我们表明,这些变体在小鼠模型中具有较弱的 iNKT 细胞刺激活性,但对人 iNKT 细胞具有显著更高的活性。我们研究中最活跃的 C4″-酰胺在部分人源化的 iNKT 细胞反应小鼠模型中显示出强烈的抗肿瘤作用。分析表明,酰胺取代基的连接长度和柔韧性影响了 iNKT 细胞抗原受体对与它们的抗原呈递分子 CD1d 结合的 C4″-酰胺取代糖脂的识别。我们的发现确立了使用稳定的 C4″-酰胺连接添加到糖部分,以进一步探索 iNKT 细胞激活糖脂的结构修饰的免疫学效应,并强调了更准确的动物模型对于评估这些化合物在人类中的免疫治疗潜力的迫切需要。

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