1] Laboratory of Immunoregulation, VIB Inflammation Research Center, 9052 Ghent, Belgium. [2] Department of Respiratory Medicine, Ghent University, 9000 Ghent, Belgium.
1] Institut Pasteur, Département d'Immunologie, Laboratoire Anticorps en Thérapie et Pathologie, 75015 Paris, France. [2] Institut National de la Santé et de la Recherche Médicale, U760, 75015 Paris, France.
Nat Rev Immunol. 2014 Feb;14(2):94-108. doi: 10.1038/nri3582. Epub 2014 Jan 21.
Dendritic cells (DCs) and macrophages use various receptors to recognize foreign antigens and to receive feedback control from adaptive immune cells. Although it was long believed that all immunoglobulin Fc receptors are universally expressed by phagocytes, recent findings indicate that only monocyte-derived DCs and macrophages express high levels of activating Fc receptors for IgG (FcγRs), whereas conventional and plasmacytoid DCs express the inhibitory FcγR. In this Review, we discuss how the uptake, processing and presentation of antigens by DCs and macrophages is influenced by FcγR recognition of immunoglobulins and immune complexes in the steady state and during inflammation.
树突状细胞(DCs)和巨噬细胞利用各种受体来识别外来抗原,并从适应性免疫细胞接收反馈控制。尽管长期以来人们一直认为所有免疫球蛋白 Fc 受体都普遍存在于吞噬细胞中,但最近的研究结果表明,只有单核细胞衍生的 DCs 和巨噬细胞表达高水平的 IgG(FcγR)激活型 Fc 受体,而常规和浆细胞样 DCs 表达抑制性 FcγR。在这篇综述中,我们讨论了在稳态和炎症期间,FcγR 识别免疫球蛋白和免疫复合物如何影响 DCs 和巨噬细胞对抗原的摄取、加工和呈递。