Increased frequencies of cochlin-specific T cells in patients with autoimmune sensorineural hearing loss

Moo-Jin Baek, Hyun-Min Park, Justin M Johnson, Cengiz Z Altuntas, Daniel Jane-Wit, Ritika Jaini, C Arturo Solares, Dawn M Thomas, Edward J Ball, Nahid G Robertson, Cynthia C Morton, Gordon B Hughes, Vincent K Tuohy

Research output: Contribution to journalArticlepeer-review

Abstract

Autoimmune sensorineural hearing loss (ASNHL) is the most common cause of sudden hearing loss in adults. Although autoimmune etiopathogenic events have long been suspected in ASNHL, inner ear-specific Ags capable of targeting T cell autoreactivity have not been identified in ASNHL. In this study, we show by ELISPOT analysis that compared with normal hearing age- and sex-matched control subjects, ASNHL patients have significantly higher frequencies of circulating T cells producing either IFN-gamma (p = 0.0001) or IL-5 (p = 0.03) in response to recombinant human cochlin, the most abundant inner ear protein. In some patients, cochlin responsiveness involved both CD4+ and CD8+ T cells whereas other patients showed cochlin responsiveness confined to CD8+ T cells. ASNHL patients also showed significantly elevated cochlin-specific serum Ab titers compared with both normal hearing age- and sex-matched control subjects and patients with noise- and/or age-related hearing loss (p < 0.05 at all dilutions tested through 1/2048). Our study is the first to show T cell responsiveness to an inner ear-specific protein in ASNHL patients, and implicates cochlin as a prominent target Ag for mediating autoimmune inner ear inflammation and hearing loss.

Original languageEnglish
Pages (from-to)4203-10
Number of pages8
JournalJournal of immunology (Baltimore, Md. : 1950)
Volume177
Issue number6
Publication statusPublished - 15 Sept 2006

Keywords

  • Aged
  • Autoimmune Diseases
  • Cells, Cultured
  • Epitopes, T-Lymphocyte
  • Extracellular Matrix Proteins
  • Female
  • Hearing Loss, Sensorineural
  • Humans
  • Male
  • Middle Aged
  • Proteins
  • Recombinant Proteins
  • T-Lymphocyte Subsets
  • Journal Article
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

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