Rockefeller University and Howard Hughes Medical Institute, New York, New York.
Rockefeller University, New York, New York.
Arthritis Rheumatol. 2017 May;69(5):986-995. doi: 10.1002/art.40035.
Most patients with rheumatoid arthritis (RA) harbor antibodies to citrullinated autoantigens such as citrullinated fibrinogen. Two isoforms of peptidylarginine deiminase (PAD), PAD type 2 (PAD2) and PAD4, which catalyze citrullination with different substrate specificities, can be detected in the synovium of RA patients. This study was undertaken to determine whether RA antibodies preferentially bind PAD2- or PAD4-citrullinated fibrinogen.
RA patient and normal donor plasma specimens were tested for binding to PAD2- or PAD4-citrullinated fibrinogen, native fibrinogen, or citrullinated fibrinogen peptides in various dilutions by enzyme-linked immunosorbent assay (ELISA) and Western blotting. Bands corresponding to masses demonstrating RA antibody reactivity by Western blotting were excised and analyzed by mass spectrometry.
At low antibody titers (1:40 and 1:100), there was no significant difference between RA antibody reactivity to PAD2- and PAD4-citrullinated fibrinogen. When plasma was further diluted to 1:250 and 1:1,000, RA patient plasma bound PAD4-citrullinated fibrinogen significantly more than PAD2-citrullinated fibrinogen, as measured by ELISA and Western blotting. An increased antibody titer was associated with increased avidity for both PAD2- and PAD4-citrullinated fibrinogen. Both enzymes hypercitrullinated fibrinogen, but PAD4 citrullinated arginines more intermittently, generating a mix of citrullinated and noncitrullinated arginines. Peptide ELISA and preadsorption assays confirmed that the region of intermittent citrullination accounts for the majority of RA antibody binding to the β-chain of citrullinated fibrinogen.
At high titers, RA antibodies preferentially bind fibrinogen modified by PAD4, because intermittent citrullination offers a more diverse assortment of citrullinated epitopes.
大多数类风湿关节炎(RA)患者体内存在针对瓜氨酸化自身抗原的抗体,如瓜氨酸化纤维蛋白原。两种肽基精氨酸脱亚氨酶(PAD)同工酶,即 PAD 型 2(PAD2)和 PAD4,可在 RA 患者的滑膜中检测到,它们具有不同的底物特异性,可催化瓜氨酸化反应。本研究旨在确定 RA 抗体是否优先结合 PAD2 或 PAD4 催化的瓜氨酸化纤维蛋白原。
通过酶联免疫吸附试验(ELISA)和 Western 印迹法检测 RA 患者和正常供体血浆标本在不同稀释度下与 PAD2 或 PAD4 瓜氨酸化纤维蛋白原、天然纤维蛋白原或瓜氨酸化纤维蛋白原肽的结合情况。Western 印迹法检测到与 RA 抗体反应的分子量对应的条带被切除并通过质谱分析。
在低抗体滴度(1:40 和 1:100)时,RA 抗体对 PAD2 和 PAD4 瓜氨酸化纤维蛋白原的反应性没有显著差异。当血浆进一步稀释至 1:250 和 1:1000 时,与 PAD2 瓜氨酸化纤维蛋白原相比,RA 患者血浆通过 ELISA 和 Western 印迹法结合 PAD4 瓜氨酸化纤维蛋白原的量显著增加。抗体滴度的增加与 PAD2 和 PAD4 瓜氨酸化纤维蛋白原的亲和力均增加有关。两种酶均过度瓜氨酸化纤维蛋白原,但 PAD4 间歇性地瓜氨酸化精氨酸,产生瓜氨酸化和非瓜氨酸化精氨酸的混合物。肽 ELISA 和预吸附实验证实,间歇性瓜氨酸化的区域占 RA 抗体结合瓜氨酸化纤维蛋白原β 链的主要部分。
在高滴度时,RA 抗体优先结合由 PAD4 修饰的纤维蛋白原,因为间歇性瓜氨酸化提供了更多样化的瓜氨酸化表位。