Department of Pharmacology, School of Medicine, Shenzhen Campus of Sun Yat-sen University, Sun Yat-sen University, Shenzhen, Guangdong, China.
Guangdong Provincial Key Laboratory of Medical Molecular Diagnostics, Key Laboratory of Stem Cell and Regenerative Tissue Engineering, School of Basic Medical Sciences, Guangdong Medical University, Dongguan, China.
Front Immunol. 2022 Nov 2;13:997287. doi: 10.3389/fimmu.2022.997287. eCollection 2022.
The pathogeny of type 1 diabetes (T1D) is mainly provoked by the β-cell loss due to the autoimmune attack. Critically, autoreactive T cells firsthand attack β-cell in islet, that results in the deficiency of insulin in bloodstream and ultimately leads to hyperglycemia. Hence, modulating immunity to conserve residual β-cell is a desirable way to treat new-onset T1D. However, systemic immunosuppression makes patients at risk of organ damage, infection, even cancers. Biomaterials can be leveraged to achieve targeted immunomodulation, which can reduce the toxic side effects of immunosuppressants. In this review, we discuss the recent advances in harness of biomaterials to immunomodulate immunity for T1D. We investigate nanotechnology in targeting delivery of immunosuppressant, biological macromolecule for β-cell specific autoreactive T cell regulation. We also explore the biomaterials for developing vaccines and facilitate immunosuppressive cells to restore immune tolerance in pancreas.
1 型糖尿病(T1D)的发病机制主要是由于自身免疫攻击导致β细胞丧失。关键的是,自身反应性 T 细胞首先攻击胰岛中的β细胞,导致血液中胰岛素缺乏,最终导致高血糖。因此,调节免疫以保留残余的β细胞是治疗新诊断的 T1D 的一种理想方法。然而,全身免疫抑制使患者面临器官损伤、感染甚至癌症的风险。生物材料可用于实现靶向免疫调节,从而减少免疫抑制剂的毒副作用。在这篇综述中,我们讨论了利用生物材料来调节免疫以治疗 T1D 的最新进展。我们研究了纳米技术在靶向递送免疫抑制剂和用于调节β细胞特异性自身反应性 T 细胞的生物大分子方面的应用。我们还探讨了用于开发疫苗和促进免疫抑制细胞恢复胰腺免疫耐受的生物材料。