PLoS Pathogens | |
Relay of Herpes Simplex Virus between Langerhans Cells and Dermal Dendritic Cells in Human Skin | |
Kerrie J. Sandgren1  Norman Olbourne1  Anthony L. Cunningham1  Min Kim1  Andrew N. Harman1  Virginia James1  Kaylene McKinnon1  Najla Nasr1  Shailandra Sawleshwarkar2  Naomi R. Truong2  Lidija Bosnjak2  Kirstie M. Bertram2  Ralph C. Cohen2  | |
[1] Centre for Virus Research, Westmead Millennium Institute, Sydney, Australia;Sydney Medical School, University of Sydney, Sydney, Australia | |
关键词: Dermis; Skin infections; Herpes simplex virus; Epidermis; Biopsy; T cells; Skin; Apoptosis; | |
DOI : 10.1371/journal.ppat.1004812 | |
学科分类:生物科学(综合) | |
来源: Public Library of Science | |
【 摘 要 】
The mechanism by which immunity to Herpes Simplex Virus (HSV) is initiated is not completely defined. HSV initially infects mucosal epidermis prior to entering nerve endings. In mice, epidermal Langerhans cells (LCs) are the first dendritic cells (DCs) to encounter HSV, but it is CD103+ dermal DCs that carry viral antigen to lymph nodes for antigen presentation, suggesting DC cross-talk in skin. In this study, we compared topically HSV-1 infected human foreskin explants with biopsies of initial human genital herpes lesions to show LCs are initially infected then emigrate into the dermis. Here, LCs bearing markers of maturation and apoptosis formed large cell clusters with BDCA3+ dermal DCs (thought to be equivalent to murine CD103+ dermal DCs) and DC-SIGN+ DCs/macrophages. HSV-expressing LC fragments were observed inside the dermal DCs/macrophages and the BDCA3+ dermal DCs had up-regulated a damaged cell uptake receptor CLEC9A. No other infected epidermal cells interacted with dermal DCs. Correspondingly, LCs isolated from human skin and infected with HSV-1 in vitro also underwent apoptosis and were taken up by similarly isolated BDCA3+ dermal DCs and DC-SIGN+ cells. Thus, we conclude a viral antigen relay takes place where HSV infected LCs undergo apoptosis and are taken up by dermal DCs for subsequent antigen presentation. This provides a rationale for targeting these cells with mucosal or perhaps intradermal HSV immunization.
【 授权许可】
CC BY
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