Antibodies to myelin protein zero (P0) protein as markers of auto-immune inner ear diseases

References

• McCabe BF. Autoimmune sensorineural hearing loss. Ann Otol Rhinol Laryngol 1979; 88: 585–589
   PubMed Web of Science ®Google Scholar
• Bernstein JM, Shanahan TC, Schaffer FM. Further observations on the role of the MHC genes and certain hearing disorders. Acta Otolaryngol 1996; 116: 666–671
   PubMed Web of Science ®Google Scholar
• Riente L, Bongiorni F, Nacci A, Migliorini P, Segnini G, Delle Sedie A, Ursino F, Tomassi S, Fattori B. Antibodies to inner ear antigens in Menière's disease. Clin Exp Immunol 2004; 135: 159–163
   PubMedGoogle Scholar
• Gloddek B, Gloddek J, Arnold W. A rat T-cell line that mediates autoimmune disease of the inner ear in the Lewis rat. ORL J Otorhinolaryngol Relat Spec 1999; 61: 181–187
   PubMedGoogle Scholar
• Yoo TJ, Stuart JM, Kang AH, Townes AS, Tomoda K, Dixit S. Type II collagen autoimmunity in otosclerosis and Menière's disease. Science 1982; 217: 1153–1155
   PubMed Web of Science ®Google Scholar
• Harris JP, Sharp PA. Inner ear autoantibodies in patients with rapidly progressive sensorineural hearing loss. Laryngoscope 1990; 100: 516–524
   PubMed Web of Science ®Google Scholar
• Gottschlich S, Billings PB, Keithley EM, Weisman MH, Harris JP. Assessment of serum antibodies in patients with rapidly progressive sensorineural hearing loss and Menière's disease. Laryngoscope 1995; 105: 1347–1352
   PubMed Web of Science ®Google Scholar
• Billings PB, Keithley EM, Harris JP. Evidence linking the 68 kilo Dalton antigen identified in progressive sensorineural hearing loss patient sera with heat shock protein 70. Ann Otol Rhinol Laryngol 1995; 104: 181–188
   PubMed Web of Science ®Google Scholar
• Cao MY, Deggouj N, Gersdorff M, Tomasi JP. Guinea pig inner ear antigens: Extraction and application to the study of human autoimmune inner ear disease. Laryngoscope 1996; 106: 207–212
   PubMedGoogle Scholar
• Cao MY, Dupiez VJ, Rider H, Deggouj N, Gersdorff M, Rousseau GG, Tomasi JP. Myelin protein P0 as a potential auto antigen in autoimmune inner ear disease. FASEB J 1996; 10: 1635–1640
   PubMed Web of Science ®Google Scholar
• Cao MY, Gersdorff M, Deggouj N, Tomasi JP. The localization and specificity of guinea pig inner ear antigenic epitopes. J Laryngol Otol 1995; 109: 19–23
   PubMedGoogle Scholar
• Khalili-Shirazi A, Atkinson P, Gregson N, Hughes RA. Antibody responses to P0 and P2 myelin proteins in Guillain–Barre syndrome and chronic idiopathic demyelinating polyradiculoneuropathy. J Neuroimmunol 1993; 46: 245–251
   PubMed Web of Science ®Google Scholar
• Milner P, Lovelidge CA, Taylor WA, Hughes RA. P0 myelin protein produces experimental allergic neuritis in Lewis rats. J Neurol Sci 1987; 79: 275–285
   PubMed Web of Science ®Google Scholar
• Committee on Hearing and Equilibrium. Committee on hearing and equilibrium guidelines for the diagnosis and evaluation of therapy in Menière's disease. Otolaryngol Head Neck Surg 1995; 113: 181–185
   PubMed Web of Science ®Google Scholar
• Passali D, Damiani V, Mora R, Passali FM, Passali GC, Bellussi L. P0 antigen detection in sudden hearing loss and Menière's disease: A new diagnostic marker ?. Acta Otolaryngol 2004; 124: 1145–1148
   PubMed Web of Science ®Google Scholar
• Nuti D, Biagini C, Salerni L, Gaudini E, Passali GC. Use of mammalian inner ear antigens for the diagnosis of autoimmune sudden loss of vestibular function. Acta Otolaryngol 2002; 548: 34–37
   Google Scholar
• Boerkoel CF, Takashima H, Garcia CA, Olney RK, Johnson J, Berry K, Russo P, Kennedy S, Teebi AS, Scavina M, Williams LL, Mancias P, Butler IJ, Krajewski K, Shy M, Lupski JR. Charcot–Marie–Tooth disease and related neuropathies: Mutation distribution and genotype–phenotype correlation. Ann Neurol 2002; 51: 190–201
   PubMed Web of Science ®Google Scholar
• Shy ME, Jani A, Krajewski K, Grandis M, Lewis RA, Li J, Shy RR, Balsamo J, Lilien J, Garbern JY, Kamholz J. Phenotypic clustering in MPZ mutations. Brain 2004; 127: 371–384
   PubMed Web of Science ®Google Scholar
• Warner LE, Hilz MJ, Appel SH, Killian JM, Kolodry EH, Karpati G, Carpenter S, Watters GV, Wheeler C, Witt D, Bodell A, Nelis E, Van Broeckhoven C, Lupski JR. Clinical phenotypes of different MPZ (P0) mutations may include Charcot–Marie–Tooth type 1B, Dejerine–Sottas, and congenital hypomyelination. Neuron 1996; 17: 451–460
   PubMed Web of Science ®Google Scholar
• Santoro L, Manganelli F, Di Maria E, Bordo D, Cassandrini D, Ajmar F, Mandich P, Bellone E. A novel mutation of myelin protein zero associated with an axonal form of Charcot–Marie–Tooth disease. J Neurol Neurosurg Psychiatry 2004; 75: 262–265
   PubMedGoogle Scholar
• Bienfait HM, Faber CG, Baas F, Gabreels-Festen AA, Koelman JH, Hoogendijk JE, Verschuuren JJ, Wokke JH, de Visser M. Late onset axonal Charcot–Marie–Tooth phenotype caused by a novel myelin protein zero mutation. J Neurol Neurosurg Psychiatry 2006; 77: 534–537
   PubMedGoogle Scholar
• Chapon F, Latour P, Diraison P, Schaeffer S, Vandenberghe A. Axonal phenotype of Charcot–Marie–Tooth disease associated with a mutation in the myelin protein zero gene. J Neurol Neurosurg Psychiatry 1999; 66: 779–782
   PubMed Web of Science ®Google Scholar
• Kilfoyle DH, Dyck PJ, Wu Y, Litchy WJ, Klein DM, Dyck PJ, Kumar N, Cunningham JM, Klein CJ. Myelin protein zero mutation His39Pro: Hereditary motor and sensory neuropathy with variable onset, hearing loss, restless legs and multiple sclerosis. J Neurol Neurosurg Psychiatry 2006; 77: 963–966
   PubMedGoogle Scholar
• Seeman P, Mazanec R, Huehne K, Suslikova P, Keller O, Rautenstrauss B. Hearing loss as the first feature of late-onset axonal CMT disease due to a novel P0 mutation. Neurology 2004; 63: 733–735
   PubMedGoogle Scholar
• Boulassel MR, Guerit JM, Denison S, de Tourtchaninoff M, Wenderickx L, Botterman N, Deggouj N, Gersdorff M, Tomasi JP. No evidence of auditory dysfunction in guinea pigs immunized with myelin P0 protein. Hear Res 2001; 152: 10–16
   PubMedGoogle Scholar