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Langerhans cells regulate immunity in adulthood by regulating postnatal dermal lymphatic development.
Sim, Ji Hyun; Bell, Richard; Feng, Zhonghui; Chyou, Susan; Shipman, William D; Kataru, Raghu P; Ivashkiv, Lionel; Mehrara, Babak; Lu, Theresa T.
Affiliation
  • Sim JH; Autoimmunity and Inflammation Program, Hospital for Special Surgery Research Institute, New York, NY 10021, USA.
  • Bell R; Department of Microbiology and Immunology, Weill Cornell Medical College, New York, NY 10065, USA.
  • Feng Z; Arthritis and Tissue Degeneration Program, Hospital for Special Surgery Research Institute, New York, NY 10021, USA.
  • Chyou S; Autoimmunity and Inflammation Program, Hospital for Special Surgery Research Institute, New York, NY 10021, USA.
  • Shipman WD; Autoimmunity and Inflammation Program, Hospital for Special Surgery Research Institute, New York, NY 10021, USA.
  • Kataru RP; Autoimmunity and Inflammation Program, Hospital for Special Surgery Research Institute, New York, NY 10021, USA.
  • Ivashkiv L; Weill Cornell/Rockefeller/Sloan-Kettering Tri-Institutional MD-PhD Program, New York, NY USA.
  • Mehrara B; Immunology and Microbial Pathogenesis Graduate Program, Weill Cornell Medicine, New York, NY, USA.
  • Lu TT; Department of Plastic Surgery, Memorial Sloan Kettering, New York, NY 10021, USA.
bioRxiv ; 2024 Jul 16.
Article in En | MEDLINE | ID: mdl-39071369
ABSTRACT
The communication between skin and draining lymph nodes is crucial for well-regulated immune responses to skin insults. The skin sends antigen and other signals via lymphatic vessels to regulate lymph node activity, and regulating dermal lymphatic function is another means to control immunity. Here, we show that Langerhans cells (LCs), epidermis-derived antigen-presenting cells, mediate dermal lymphatic expansion and phenotype acquisition postnatally, a function is independent of LC entry into lymphatic vessels. This postnatal LC-lymphatic axis serves in part to control inflammatory systemic T cell responses in adulthood. Our data provide a tissue-based mechanism by which LCs regulate T cells remotely across time and space and raise the possibility that immune diseases in adulthood could reflect compromise of the LC-lymphatic axis in childhood.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: BioRxiv Year: 2024 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: BioRxiv Year: 2024 Document type: Article Affiliation country: United States Country of publication: United States