Atassi M Z, Ruan K H, Jinnai K, Oshima M, Ashizawa T
Department of Biochemistry, Baylor College of Medicine, Houston.
Proc Natl Acad Sci U S A. 1992 Jul 1;89(13):5852-6. doi: 10.1073/pnas.89.13.5852.
A synthetic peptide corresponding to a myasthenogenic region of Torpedo californica acetylcholine (AcCho) receptor (AcChoR) alpha subunit, AcChoR alpha-(125-148), was conjugated to monomethoxypolyethylene glycol (mPEG). Injection of mice with the mPEG-AcChoR alpha-(125-148) conjugate and subsequent immunization with whole Torpedo AcChoR suppressed the development of experimental autoimmune myasthenia gravis (EAMG) by electrophysiological criteria. In anti-AcChoR sera from these animals, the antibody response against unconjugated AcChoR alpha-(125-148) was decreased, while the antibody responses against whole AcChoR and other epitopes were not altered. There were no detectable changes in T-cell proliferation responses to AcChoR alpha-(125-148) or to whole AcChoR in these animals. Prior injections with a "nonsense" peptide-mPEG conjugate had no effect on responses to the subsequent immunization with whole Torpedo AcChoR. The results indicate that the mPEG-AcChoR alpha-(125-148) conjugate has epitope-specific tolerogenicity for antibody responses in EAMG and that the AcChoR alpha-subunit region comprising residues 125-148 plays an important pathophysiological role in EAMG. The epitope-directed tolerogenic conjugates may be useful for future immunotherapies of human myasthenia gravis. The strategy of specific suppression of the antibody response to a predetermined epitope by using a synthetic mPEG-peptide conjugate may prove useful in manipulation and suppression of unwanted immune responses such as autoimmunity and allergy.
一种与加州电鳐乙酰胆碱(AcCho)受体(AcChoR)α亚基的致重症肌无力区域相对应的合成肽,即AcChoRα-(125 - 148),与单甲氧基聚乙二醇(mPEG)偶联。给小鼠注射mPEG-AcChoRα-(125 - 148)偶联物,随后用完整的加州电鳐AcChoR进行免疫,根据电生理标准,可抑制实验性自身免疫性重症肌无力(EAMG)的发展。在这些动物的抗AcChoR血清中,针对未偶联的AcChoRα-(125 - 148)的抗体反应降低,而针对完整AcChoR和其他表位的抗体反应未改变。这些动物对AcChoRα-(125 - 148)或完整AcChoR的T细胞增殖反应没有可检测到的变化。预先注射“无意义”肽-mPEG偶联物对随后用完整的加州电鳐AcChoR进行免疫的反应没有影响。结果表明,mPEG-AcChoRα-(125 - 148)偶联物对EAMG中的抗体反应具有表位特异性耐受性,并且包含125 - 148位残基的AcChoRα亚基区域在EAMG中起重要的病理生理作用。表位导向的耐受性偶联物可能对未来人类重症肌无力的免疫治疗有用。使用合成的mPEG-肽偶联物特异性抑制针对预定表位的抗体反应的策略可能在操纵和抑制不需要的免疫反应如自身免疫和过敏方面证明是有用的。