决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Tumor-associated Tn and STn antigens: from molecular mechanism to precision diagnosis and treatment.
Tn/STn 抗原在肿瘤发生和免疫逃逸中发挥关键作用,在诊断和治疗方面具有巨大潜力。未来研究应集中于阐明其潜在机制、开发创新检测技术,并促进多学科合作,以推动基于 Tn/STn 抗原的肿瘤分子分型、精准靶向治疗和疗效预测系统的发展,从而为癌症诊断和治疗提供新方向。
异常蛋白糖基化是肿瘤的关键特征。在这些修饰中,Tn抗原(GalNAc 1-Ser/Thr)及其唾液酸化衍生物STn抗原(Neu5Ac 2-6GalNAc 1-O-Ser/Thr)是突出的肿瘤相关碳水化合物抗原。这些抗原在上皮恶性肿瘤中异常积累,包括结直肠癌、乳腺癌和胰腺癌。其病理性过表达主要源于COSMC/T-合酶轴的失活,这可能是由基因突变或表观遗传沉默引起,导致O-聚糖生物合成截短。
Tn/STn 抗原通过激活致癌信号通路(如 EGFR/FAK)和诱导上皮-间质转化,直接促进肿瘤进展。此外,这些抗原在肿瘤微环境的免疫抑制中发挥显著作用。Tn 抗原与髓系细胞上的巨噬细胞半乳糖特异性凝集素(MGL)结合,而 STn 抗原与唾液酸结合免疫球蛋白样凝集素(Siglecs)相互作用,共同抑制NK 细胞细胞毒性、树突状细胞成熟和 T 细胞活化。糖蛋白肿瘤标志物(如 CA15-3 和 CA125)血清水平的变化与癌细胞中异常蛋白质糖基化相关,这可能影响其表达水平、稳定性或免疫检测。当前的治疗方法包括单克隆抗体(如 Remab6、L2A5)、抗体-药物偶联物、CAR-T 细胞疗法和疫苗。然而,由于糖链异质性和低免疫原性,挑战依然存在。
BACKGROUND: Abnormal protein glycosylation is a key feature of tumors. Among the modifications, Tn antigen (GalNAc 1-Ser/Thr) and its sialylated derivative, STn antigen (Neu5Ac 2-6GalNAc 1-O-Ser/Thr), are prominent tumor-associated carbohydrate antigens. These antigens exhibit abnormal accumulation in epithelial malignancies, including colorectal cancer, breast cancer, and pancreatic cancer. Their pathological overexpression primarily stems from inactivation of the COSMC/T-synthase axis, either due to genetic mutations or epigenetic silencing, leading to truncated O-glycan biosynthesis. FINDINGS: Tn/STn antigens directly promote tumor progression by activating oncogenic signaling pathways (e.g., EGFR/FAK) and inducing epithelial-mesenchymal transition. Additionally, these antigens play a noticeable role in immune suppression in the tumor microenvironment. Tn antigens bind to macrophage galactose-specific lectin (MGL) on myeloid cells, while STn antigens interact with sialic acid-binding immunoglobulin-like lectins (Siglecs), collectively inhibiting natural killer cell cytotoxicity, dendritic cell maturation, and T cell activation. Changes in serum levels of glycoprotein tumor markers (e.g., CA15-3 and CA125) are associated with aberrant protein glycosylation in cancer cells, which may influence their expression levels, stability, or immunodetection. Current therapeutic approaches include monoclonal antibodies (e.g., Remab6, L2A5), antibody-drug conjugates, CAR-T cell therapies, and vaccines. However, challenges remain due to glycan heterogeneity and low immunogenicity. CONCLUSION: Tn/STn antigens play a pivotal role in tumorigenesis and immune evasion, presenting significant potential for both diagnostic and therapeutic applications. Future research should concentrate on elucidating the underlying mechanisms, developing innovative detection technologies, and promoting multidisciplinary collaborations to advance Tn/STn antigen-based tumor molecular subtyping, precision targeted therapies, and efficacy prediction systems, thereby providing new directions for cancer diagnosis and treatment.
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