Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY, United States.
Experimental Immunology Unit, Division of Immunology, Transplantation and Infectious Diseases, San Raffaele Scientific Institute, Milano, Italy.
Front Immunol. 2022 Oct 3;13:1011209. doi: 10.3389/fimmu.2022.1011209. eCollection 2022.
Invariant natural killer T (iNKT) cells mediate immune responses when stimulated by glycolipid agonists presented by CD1d. In extensive studies of synthetic analogues of α-galactosyl ceramides, we identified numerous examples of significant differences in the recognition of specific glycolipids in wild type mice versus human iNKT cell clones or PBMC samples. To predict human iNKT cell responses more accurately in a mouse model, we derived a mouse line in which compound genetic modifications were used to express a human-like iNKT cell TCR along with human CD1d in place of the endogenous mouse proteins. Detailed transcriptional and phenotypic profiling demonstrated that these partially humanized mice developed an expanded population of T cells recognizing CD1d-presented glycolipid antigens, among which a subset characterized by expression of chemokine receptor CXCR6 had features characteristic of authentic iNKT cells. Responses to iNKT cell activating glycolipids in these mice generated cytokine production and that showed a pattern of fine specificity that closely resembled that of cultured human iNKT cell clones. Anti-tumor responses to variants of α-galactosyl ceramide in VαKI mice also correlated with their potency for stimulating human iNKT cells. This genetically modified mouse line provides a practical model for human presentation and recognition of iNKT cell activators in the context of a normally functioning immune system, and may furnish valuable opportunities for preclinical evaluation of iNKT cell-based therapies.
不变自然杀伤 T(iNKT)细胞在受到 CD1d 呈递的糖脂激动剂刺激时介导免疫反应。在对α-半乳糖神经酰胺的合成类似物进行广泛研究时,我们在野生型小鼠与人类 iNKT 细胞克隆或 PBMC 样本对特定糖脂的识别中发现了许多明显差异的例子。为了在小鼠模型中更准确地预测人类 iNKT 细胞反应,我们构建了一种小鼠品系,其中通过复合遗传修饰表达了一种类似人类的 iNKT 细胞 TCR 以及人 CD1d,以替代内源性的小鼠蛋白。详细的转录和表型分析表明,这些部分人源化小鼠发展出了一群能够识别 CD1d 呈递的糖脂抗原的 T 细胞,其中一部分特征是表达趋化因子受体 CXCR6,具有真正 iNKT 细胞的特征。这些小鼠对 iNKT 细胞激活糖脂的反应产生了细胞因子的产生,其精细特异性模式与培养的人类 iNKT 细胞克隆非常相似。在 VαKI 小鼠中,α-半乳糖神经酰胺变体的抗肿瘤反应也与其刺激人类 iNKT 细胞的能力相关。这种遗传修饰的小鼠品系为在正常免疫系统背景下展示和识别 iNKT 细胞激活剂提供了一种实用模型,并可能为 iNKT 细胞为基础的治疗方法的临床前评估提供宝贵机会。