Wu Juan, Horuzsko Anatolij
Center for Molecular Chaperone/Radiobiology and Cancer Virology, Department of Medicine, Medical College of Georgia, Augusta, Georgia, USA.
Hum Immunol. 2009 May;70(5):353-6. doi: 10.1016/j.humimm.2009.01.024.
The expression of inhibitory immunoglobulin-like transcripts (ILTs) on dendritic cells (DCs) is a biomarker of tolerogenic DCs. In this article we discuss current knowledge on the function of ILTs and explore the molecular mechanisms involved in modulation of DCs via the inhibitory receptor and its natural ligand, rendering these cells tolerogenic. We propose a method to enhance targeting of inhibitory receptors on DCs using microparticles containing a preferential ligand, HLA-G, and monoclonal antibody against the pan-DCs marker CD11c. The double-coated microparticles increase the binding of ILT4 receptor and improve modulation of DCs in vitro and in vivo. This targeting concept can be used for regulation of specific immune responses to antigens in transplantation, autoimmunity, allergy, and cancer.
树突状细胞(DCs)上抑制性免疫球蛋白样转录物(ILTs)的表达是耐受性DCs的生物标志物。在本文中,我们讨论了关于ILTs功能的当前知识,并探索了通过抑制性受体及其天然配体调节DCs的分子机制,使这些细胞具有耐受性。我们提出了一种方法,使用含有优先配体HLA-G和抗全DCs标志物CD11c单克隆抗体的微粒来增强对DCs上抑制性受体的靶向作用。这种双层包被的微粒增加了ILT4受体的结合,并在体外和体内改善了DCs的调节。这种靶向概念可用于调节移植、自身免疫、过敏和癌症中对抗原的特异性免疫反应。