Williams R C, Malone C C, Tsuchiya N
Department of Medicine, University of Florida, Gainesville 32610.
J Immunol. 1992 Aug 1;149(3):1104-13.
IgM rheumatoid factors (RF) from 18 sera of rheumatoid arthritis (RA) patients isolated from monomeric IgG affinity columns showed strongly positive ELISA reactions with human beta 2-microglobulin (beta 2m), as well as with recombinant beta 2m. When the same RA sera were adsorbed to beta 2m-Sepharose affinity columns, eluted material showed predominant IgM anti-Fc of IgG and anti-beta 2m reactivity. Inhibition reactions with "RF" obtained from IgG affinity columns showed slightly higher reactivity of RF for Fc over beta 2m; however, when RF from the same RA serum had been adsorbed to and eluted from beta 2m affinity columns, beta 2m showed greater inhibition than Fc for RF reacting with either beta 2m or Fc on ELISA plates. Thus two overlapping populations of RF were identified in RA sera showing reactivity with both beta 2m and Fc of IgG. When RF were isolated from IgG columns, affinity was slightly higher for Fc than beta 2m. Conversely, RF eluted from beta 2m Sepharose reacted slightly more with beta 2 m than Fc. Trypsin digests of a polyclonal RA IgM RF showed no beta 2m reactivity in Fc mu 5 fragments. Fab mu RF retained slight anti-Fc IgG but no residual anti-beta 2m activity. Monoclonal human IgM, IgG, or IgA RF either from mixed cryoglobulins or EBV-stimulated RA lymphoid cell lines showed negative or occasional weakly positive anti-beta 2m activity. Overlapping 7-mer peptide ELISA analysis of the entire 99-amino acid sequence of beta 2m showed a major RF-reactive linear hydrophilic sequence at positions 56-60 which included a 3-amino acid exact homology to positions 401, 403, and 404 of the C gamma 3 domain. A peptide encompassing this sequence produced 90% inhibition of RF binding to whole beta 2m. Substitution of neutral glycines for each amino acid throughout the reactive epitope at positions 56-66 indicated that lysine at position 58 aspartic acid at 59, and tryptophane at 60 represented major portions of the RF-reactive epitope. These findings indicate that human RF derived from patients with RA react with other epitopes besides those present on IgG Fc, including epitopes on human beta 2m. For many years serum RF3 found in patients with RA have been regarded as premier examples of autoantibodies to autologous IgG.(ABSTRACT TRUNCATED AT 400 WORDS)
从单体IgG亲和柱分离得到的18例类风湿关节炎(RA)患者血清中的IgM类风湿因子(RF),与人β2-微球蛋白(β2m)以及重组β2m在ELISA反应中呈强阳性。当相同的RA血清吸附到β2m-琼脂糖亲和柱上时,洗脱物显示出主要为IgM抗IgG Fc和抗β2m反应性。用从IgG亲和柱获得的“RF”进行的抑制反应显示,RF对Fc的反应性略高于β2m;然而,当来自同一RA血清的RF吸附到β2m亲和柱上并洗脱后,在ELISA板上,β2m对与β2m或Fc反应的RF的抑制作用大于Fc。因此,在RA血清中鉴定出两个重叠的RF群体,它们与IgG的β2m和Fc均有反应性。当从IgG柱分离RF时,其对Fc的亲和力略高于β2m。相反,从β2m琼脂糖洗脱的RF与β2m的反应略多于Fc。多克隆RA IgM RF的胰蛋白酶消化产物在Fcμ5片段中未显示β2m反应性。FabμRF保留了轻微的抗IgG Fc活性,但没有残留的抗β2m活性。来自混合冷球蛋白或EBV刺激的RA淋巴细胞系的单克隆人IgM、IgG或IgA RF显示出阴性或偶尔弱阳性的抗β2m活性。对β2m完整的99个氨基酸序列进行重叠7聚体肽ELISA分析,发现在56-60位有一个主要的RF反应性线性亲水序列,其中包括与Cγ3结构域401、403和404位的3个氨基酸完全同源。包含该序列的肽对RF与完整β2m的结合产生90%的抑制作用。在56-66位反应表位的每个氨基酸用中性甘氨酸替代,表明58位的赖氨酸、59位的天冬氨酸和60位的色氨酸代表RF反应表位的主要部分。这些发现表明,来自RA患者的人RF除了与IgG Fc上的表位反应外,还与其他表位反应,包括人β2m上的表位。多年来,在RA患者血清中发现的血清RF3一直被视为自身IgG自身抗体的主要例子。(摘要截短于400字)