| Literature DB >> 25829231 |
Ryuta Kamekura1, Katsunori Shigehara2, Satsuki Miyajima3, Sumito Jitsukawa1, Koji Kawata4, Keiji Yamashita1, Tomonori Nagaya1, Ayako Kumagai4, Akinori Sato4, Hiroshi Matsumiya5, Noriko Ogasawara5, Nobuhiko Seki5, Kenichi Takano5, Yasuo Kokai6, Hiroki Takahashi3, Tetsuo Himi5, Shingo Ichimiya7.
Abstract
Allergic rhinitis (AR), the most common allergic disorder of the airway, is often accompanied by bronchial asthma. However, little is known about the mechanism by which AR advances to AR comorbid with bronchial asthma (AR+Asthma). To determine the pathophysiologic features of AR and AR+Asthma, we examined subsets of follicular helper T (Tfh) cells and regulatory B (Breg) cells in peripheral blood from AR and AR+Asthma patients. The results showed polarization of Tfh2 cells within Tfh cell subsets in both AR and AR+Asthma cases. Interestingly, the %Breg cells in total B cells were decreased in AR cases and, more extensively, in AR+Asthma cases. Moreover, we found significant correlations of fractional exhaled nitric oxide and blood eosinophil levels with the index %Tfh2 cells per %Breg cells. Our findings indicate that relative decrease in Breg cells under the condition of Tfh2 cell skewing is a putative exaggerating factor of AR to bronchial asthma.Entities:
Keywords: Allergic rhinitis; Bronchial asthma; Regulatory B cells; Tfh cells; Tfh2 cells
Mesh:
Year: 2015 PMID: 25829231 DOI: 10.1016/j.clim.2015.02.016
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969