BDCA1-positive dendritic cells (DCs) represent a unique human myeloid DC subset that induces innate and adaptive immune responses to Staphylococcus aureus Infection

• Published in: Infection and immunity 2014-11, Vol.82 (11), p.4466-4476
• Main Authors: Jin, Jun-O, Zhang, Wei, Du, Jiang-Yuan, Yu, Qing
• Format: Article
• Language: English
• Subjects: Adaptive Immunity - physiology; Adult; Antibodies; Antigens, CD1 - genetics; Antigens, CD1 - metabolism; Bacterial Infections; Cells, Cultured; Dendritic Cells - classification; Dendritic Cells - drug effects; Dendritic Cells - physiology; Female; Gene Expression Regulation - physiology; Glycoproteins - genetics; Glycoproteins - metabolism; Humans; Immunity, Innate - physiology; Male; Scavenger Receptors, Class A - genetics; Scavenger Receptors, Class A - metabolism; Signal Transduction - immunology; Staphylococcus aureus; Staphylococcus aureus - physiology; Toll-Like Receptor 2 - genetics; Toll-Like Receptor 2 - metabolism; Young Adult
• ISSN: 0019-9567; 1098-5522
• DOI: 10.1128/IAI.01851-14

Staphylococcus aureus bloodstream infection (bacteremia) is a major cause of morbidity and mortality and places substantial cost burdens on health care systems. The role of peripheral blood dendritic cells (PBDCs) in the immune responses against S. aureus infection has not been well characterized. In this study, we demonstrated that BDCA1(+) myeloid DCs (mDCs) represent a unique PBDC subset that can induce immune responses against S. aureus infection. BDCA1(+) mDCs could engulf S. aureus and strongly upregulated the expression of costimulatory molecules and production of proinflammatory cytokines. Furthermore, BDCA1(+) mDCs expressed high levels of major histocompatibility complex (MHC) class I and II molecules in response to S. aureus and greatly promoted proliferation and gamma interferon (IFN-γ) production in CD4 and CD8 T cells. Moreover, BDCA1(+) mDCs expressed higher levels of Toll-like receptor 2 (TLR-2) and scavenger receptor A (SR-A) than those on CD16(+) and BDCA3(+) mDCs, and these two receptors were both required for the recognition of S. aureus and the subsequent activation of BDCA1(+) mDCs. Finally, BDCA1(+) mDC-mediated immune responses against S. aureus were dependent on MyD88 signaling pathways. These results demonstrate that human BDCA1(+) mDCs represent a unique subset of mDCs that can respond to S. aureus to undergo maturation and activation and to induce Th1 and Tc1 immune responses.