Author/Authors :
Zhou، نويسنده , , Bin and Kermany، نويسنده , , Mohammad Habiby and Glickstein، نويسنده , , Jonathan and Cai، نويسنده , , Qing and Cai، نويسنده , , Chun and Zhou، نويسنده , , Yixuan and Nair، نويسنده , , Usha and Kim، نويسنده , , Jun Woo and Kim، نويسنده , , Patrick and Liu، نويسنده , , Wenxia and Kanangat، نويسنده , , Siva and Yoo، نويسنده , , Tai June، نويسنده ,
Abstract :
Autoimmune inner ear disease is described as progressive, bilateral although asymmetric, sensorineural hearing loss and can be improved by immunosuppressive therapy. We showed that the inner ear autoantigen β-tubulin is capable of inducing experimental autoimmune hearing loss (EAHL) in mice. Immunization of BALB/c mice with β-tubulin resulted in hair cell loss and hearing loss, effects that were not seen in animals immunized with control peptide. Moreover, the EAHL model showed that β-tubulin responsiveness involved CD4+ T cells producing IFN-γ, and T cell mediation of EAHL was determined by significantly increased auditory brainstem response after adoptive transfer of β-tubulin-activated CD4+ T cells into naive BALB/c recipients. The potential mechanisms responsible for the observed pathology of EAHL can be attributed to decreased frequency and impaired suppressive function of regulatory T cells. Our study suggests that EAHL may be a T cell-mediated organ-specific autoimmune disorder of the inner ear.