Jaume J C, Parkes A B, Lazarus J H, Hall R, Costante G, McLachlan S M, Rapoport B
Thyroid Molecular Biology Unit, Veterans Administration Medical Center, San Francisco, California 94121.
J Clin Endocrinol Metab. 1995 Mar;80(3):1000-5. doi: 10.1210/jcem.80.3.7533767.
It is not known whether epitopes recognized by autoantibodies in an individual remain constant or change over time, especially during perturbations of the humoral immune response. To address this question, we studied the epitopic profile ("fingerprint") of autoantibodies to thyroid peroxidase (TPO) in the sera of 19 women during the postpartum period. Fingerprints were determined in competition studies using 4 recombinant F(ab). At delivery and at 3 time intervals over the subsequent 9-12 months, the pool of F(ab) inhibited autoantibody binding to TPO by 80-100%, consistent with the definition by these F(ab) of a TPO immunodominant region (A1, A2, B1, and B2 domains). Despite a wide spectrum among individuals, the TPO epitopic fingerprints for all 19 women were relatively unchanged throughout the postpartum period. Fingerprint constancy occurred regardless of fluctuations in serum TPO autoantibody levels. When assessed numerically as a ratio of inhibition by the A domain F(ab) to inhibition by the B domain F(ab), the A/B domain ratios in individual women ranged from 0.2 (predominantly B domain) to more than 3.0 (predominantly A domain). However, for each individual woman, the A/B epitopic ratio was conserved throughout the study interval. Our TPO autoantibody epitopic fingerprint data have potential implications for understanding the humoral autoimmune response in man. First, the present study indicates a remarkable lack of spreading of B cell epitopes during a state of perturbation of the immune system over a period of 1 yr. Second, and perhaps more important, despite marked variations in TPO epitopic profiles among different individuals, their constancy over time suggests that TPO autoantibody fingerprints may be inherited.
尚不清楚个体中自身抗体识别的表位是保持不变还是随时间变化,尤其是在体液免疫反应受到干扰期间。为了解决这个问题,我们研究了19名女性产后血清中抗甲状腺过氧化物酶(TPO)自身抗体的表位谱(“指纹”)。在竞争研究中使用4种重组F(ab)确定指纹。在分娩时以及随后9至12个月的3个时间间隔,F(ab)池抑制自身抗体与TPO结合的比例为80%至100%,这与这些F(ab)对TPO免疫显性区域(A1、A2、B1和B2结构域)的定义一致。尽管个体之间存在广泛差异,但所有19名女性的TPO表位指纹在整个产后期间相对不变。无论血清TPO自身抗体水平如何波动,指纹稳定性均会出现。当以A结构域F(ab)的抑制率与B结构域F(ab)的抑制率之比进行数值评估时,个体女性的A/B结构域比值范围从0.2(主要为B结构域)到超过3.0(主要为A结构域)。然而,对于每一位个体女性,A/B表位比值在整个研究期间都是保守的。我们的TPO自身抗体表位指纹数据对于理解人类体液自身免疫反应具有潜在意义。首先,本研究表明在免疫系统受到干扰的1年期间,B细胞表位明显缺乏扩散。其次,也许更重要的是,尽管不同个体之间TPO表位谱存在显著差异,但它们随时间的稳定性表明TPO自身抗体指纹可能是可遗传的。