Dudziak Diana, Kamphorst Alice O, Heidkamp Gordon F, Buchholz Veit R, Trumpfheller Christine, Yamazaki Sayuri, Cheong Cheolho, Liu Kang, Lee Han-Woong, Park Chae Gyu, Steinman Ralph M, Nussenzweig Michel C
Laboratory of Molecular Immunology, The Rockefeller University, New York, NY 10021, USA.
Science. 2007 Jan 5;315(5808):107-11. doi: 10.1126/science.1136080.
Dendritic cells (DCs) process and present self and foreign antigens to induce tolerance or immunity. In vitro models suggest that induction of immunity is controlled by regulating the presentation of antigen, but little is known about how DCs control antigen presentation in vivo. To examine antigen processing and presentation in vivo, we specifically targeted antigens to two major subsets of DCs by using chimeric monoclonal antibodies. Unlike CD8+ DCs that express the cell surface protein CD205, CD8- DCs, which are positive for the 33D1 antigen, are specialized for presentation on major histocompatibility complex (MHC) class II. This difference in antigen processing is intrinsic to the DC subsets and is associated with increased expression of proteins involved in MHC processing.
树突状细胞(DCs)处理并呈递自身和外来抗原以诱导耐受或免疫。体外模型表明,免疫诱导是通过调节抗原呈递来控制的,但对于DCs在体内如何控制抗原呈递知之甚少。为了研究体内的抗原处理和呈递,我们通过使用嵌合单克隆抗体将抗原特异性靶向DCs的两个主要亚群。与表达细胞表面蛋白CD205的CD8⁺ DCs不同,对33D1抗原呈阳性的CD8⁻ DCs专门用于在主要组织相容性复合体(MHC)II类上呈递。这种抗原处理的差异是DC亚群所固有的,并且与参与MHC处理的蛋白质表达增加有关。