| Literature DB >> 28916523 |
Ryuta Kamekura1,2, Kenichi Takano2, Motohisa Yamamoto3, Koji Kawata4, Katsunori Shigehara4, Sumito Jitsukawa4,2, Tomonori Nagaya2, Fumie Ito4,2, Akinori Sato4, Noriko Ogasawara2, Chieko Tsubomatsu2, Hiroki Takahashi3, Hiroshi Nakase5, Tetsuo Himi2, Shingo Ichimiya4.
Abstract
IgG4-related disease (IgG4-RD) is a newly recognized systemic chronic fibroinflammatory disease. However, the pathogenesis of IgG4-RD remains unknown. To determine the pathophysiologic features of IgG4-RD, we examined T follicular helper (Tfh) cells in lesions and blood from patients with IgG4-RD. Patients with IgG4-related dacryoadenitis and sialadenitis (IgG4-DS) showed increased infiltration of Tfh cells highly expressing programmed death 1 and ICOS in submandibular glands. Tfh cells from IgG4-DS submandibular glands had higher expression of B cell lymphoma 6 and a greater capacity to help B cells produce IgG4 than did tonsillar Tfh cells. We also found that the percentage of programmed death 1hi circulating Tfh cells in IgG4-DS patients was higher than that in healthy volunteers and was well correlated with clinical parameters. Our findings indicate that anomalous Tfh cells in tissue lesions of IgG4-RD have features distinct from those in lymphoid counterparts or blood and potentially regulate local IgG4 production in IgG4-RD.Entities:
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Year: 2017 PMID: 28916523 DOI: 10.4049/jimmunol.1601507
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422