Literature DB >> 9508029

Failure of elevated heat shock protein 70 antibodies to alter cochlear function in mice.

D R Trune1, J B Kempton, C R Mitchell, S H Hefeneider.   

Abstract

Heat shock protein 70 (HSP70) has been suggested as the putative cochlear antigen underlying a proposed autoimmune etiology in certain cases of Meniere's disease and idiopathic hearing loss. To determine if antibodies to this cellular protein are capable of altering cochlear function, BALB/c (N= 3) and CBA/J (N= 9) mice were inoculated with bovine HSP70 by intraperitoneal injections (10 microg in saline) every 10 days for 7 or 10 months, respectively. An equal number of control mice were injected with PBS according to the same schedule. ABR thresholds at 4, 8, 16, and 32 kHz in the HSP70-inoculated mice did not change over the 10 month period and were similar to saline controls. Furthermore, serum immune complexes and antinuclear antibodies did not increase over the inoculation period. ELISA analysis demonstrated the mice created antibodies to the foreign HSP70, but these apparently caused no abnormalities in the auditory or immune systems. It was concluded that foreign HSP70 is antigenic and inoculation with it will raise antibodies, but these antibodies were neither immunopathogenic nor cochleopathic. Therefore, these findings do not support current theories that elevated anti-HSP70 antibodies are the underlying cause of hearing loss in patients with such antibodies present.

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Year:  1998        PMID: 9508029     DOI: 10.1016/s0378-5955(97)00198-6

Source DB:  PubMed          Journal:  Hear Res        ISSN: 0378-5955            Impact factor:   3.208


  4 in total

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Authors:  J T Roland
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3.  Autoantibodies to recombinant human CTL2 in autoimmune hearing loss.

Authors:  Pavan K Kommareddi; Thankam S Nair; Mounica Vallurupalli; Steven A Telian; H Alexander Arts; Hussam K El-Kashlan; Robert T Sataloff; Thomas E Carey
Journal:  Laryngoscope       Date:  2009-05       Impact factor: 3.325

4.  Alternate splicing of interleukin-1 receptor type II (IL1R2) in vitro correlates with clinical glucocorticoid responsiveness in patients with AIED.

Authors:  Andrea Vambutas; James DeVoti; Elliot Goldofsky; Michael Gordon; Martin Lesser; Vincent Bonagura
Journal:  PLoS One       Date:  2009-04-29       Impact factor: 3.240

  4 in total

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