Section of Rheumatology, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06520, USA.
Section of Rheumatology, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06520, USA.
Mol Immunol. 2014 Mar;58(1):56-65. doi: 10.1016/j.molimm.2013.10.013. Epub 2013 Dec 3.
The cooperation of B lymphocytes with other antigen presenting cells (APCs) is often necessary in the efficient processing and presentation of antigen. Herein, we describe a mechanism by which B cells physically interact with dendritic cells (DCs) resulting in the transfer of B cell receptor (BCR)-enriched antigen to these APCs. Antigen transfer involves direct contact between the two cells followed by the capture of B cell derived membrane and intracellular components. Strikingly, DCs acquire greater amounts of antigen by transfer from B cells than by endocytosis of free antigen. Blocking scavenger receptor A, a DC surface receptor involved in membrane acquisition, abrogates these events. We propose that antigen transfer from B cells to DCs results in a more focused immunologic response due to the selective editing of Ag by the BCR.
B 淋巴细胞与其他抗原呈递细胞 (APCs) 的合作通常是抗原有效处理和呈递所必需的。在此,我们描述了一种 B 细胞与树突状细胞 (DCs) 发生物理相互作用的机制,导致 B 细胞受体 (BCR)-富集抗原转移到这些 APC 中。抗原转移涉及到两细胞之间的直接接触,随后捕获 B 细胞衍生的膜和细胞内成分。引人注目的是,与内吞游离抗原相比,通过从 B 细胞转移,DC 获得更多的抗原。阻断参与膜摄取的 DC 表面受体清道夫受体 A,可消除这些事件。我们提出,B 细胞向 DC 转移抗原会导致更有针对性的免疫反应,因为 BCR 对 Ag 进行了选择性编辑。