Volpé R
Ann Intern Med. 1977 Jul;87(1):86-99. doi: 10.7326/0003-4819-87-1-86.
There is considerable evidence to suggest that the organspecific autoimmune endocrinopathies are primary disorders of the lympoid system. Although proof is not complete, the basic genetic defect in each condition may be one of immune surveillance, that is, a defect in suppressor "T" lymphocytes. Combinations of two or more of these conditions may be due to the concurrence of two or more specific defects in immune control, as well as the random appearance of the appropriate self-directed "forbidden" clones of lymphocytes. In this concept, there is no need for antigenic alteration (only antigenic availability) to initiate these disorders. Both cell-mediated and humoral immunity seem essential, with roles for immune complexes and "killer" cells as well. Antireceptor antibodies are of particular interest in Graves' disease, where they are stimulatory: other antireceptor antibodies have been found that are blocking antibodies, and others may merely bind without either stimulating or blocking.
有大量证据表明,器官特异性自身免疫性内分泌病是淋巴系统的原发性疾病。虽然证据并不完整,但每种疾病的基本遗传缺陷可能是免疫监视缺陷之一,即抑制性“T”淋巴细胞缺陷。两种或更多种这些疾病的组合可能是由于免疫控制中两种或更多种特定缺陷的同时存在,以及适当的自身导向“禁忌”淋巴细胞克隆的随机出现。按照这个概念,引发这些疾病无需抗原改变(只需抗原可及性)。细胞介导免疫和体液免疫似乎都必不可少,免疫复合物和“杀伤”细胞也发挥作用。抗受体抗体在格雷夫斯病中特别受关注,在该病中它们具有刺激作用:还发现了其他抗受体抗体是阻断抗体,还有一些可能只是结合而不产生刺激或阻断作用。