Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire.
Dartmouth College, Hanover, New Hampshire.
Arthritis Rheumatol. 2017 Jul;69(7):1381-1386. doi: 10.1002/art.40098. Epub 2017 Jun 5.
Anti-carbamylated protein (anti-CarP) antibodies are associated with the risk and severity of rheumatoid arthritis (RA) and are primarily directed against fibrinogen. The lack of understanding of anti-CarP antibody reactivity has limited analysis of the immunopathogenic associations in RA. To address this shortcoming, we mapped anti-CarP antibody epitope reactivity in RA patient sera.
Immunoblotting identified a patient serum sample with specific reactivity to the carbamylated human fibrinogen β-chain. Liquid chromatography mass spectrometry (LC-MS) identified sites of homocitrullines (carbamylated lysines) present in the human fibrinogen β-chain. The reactivity of an anti-CarP antibody-positive cohort to specific peptides containing carbamylated lysines was determined by enzyme-linked immunosorbent assay, through direct binding (n = 63 sera) and by competition assays (n = 40 sera).
Serum with specific reactivity to carbamylated, but not citrullinated, fibrinogen β-chain was identified in a specimen obtained from an RA patient. LC-MS identified carbamylation of 9 of 34 lysines in the human fibrinogen β-chain. Mapping of immunoreactivity to tryptic peptide fragments demonstrated several candidate carbamylated epitopes that were confirmed by competition experiments. Peptides containing a homocitrulline at position 83 appeared to be an immunodominant epitope in some RA patient sera, with additional reactivity to peptides containing homocitrullines at positions 52, 264, 351, 367, and 374.
Anti-CarP antibodies appear to preferentially target specific regions of the human fibrinogen β-chain that contain homocitrullines. Interestingly, humoral immunoreactivity appears to be relatively restricted in some patients, which may enable detection of specific relationships with disease phenotype.
抗氨甲酰化蛋白(anti-CarP)抗体与类风湿关节炎(RA)的风险和严重程度相关,主要针对纤维蛋白原。由于对 anti-CarP 抗体反应性缺乏了解,限制了 RA 中免疫发病机制关联的分析。为了解决这一不足,我们对 RA 患者血清中的 anti-CarP 抗体表位反应性进行了作图。
免疫印迹鉴定了一份具有特定纤维蛋白原β链氨甲酰化反应性的患者血清样本。液相色谱-质谱(LC-MS)鉴定了人纤维蛋白原β链中存在的同型瓜氨酸(氨甲酰化赖氨酸)的位置。通过酶联免疫吸附试验(ELISA),通过直接结合(n=63 份血清)和竞争试验(n=40 份血清),确定了抗 CarP 抗体阳性队列对含有氨甲酰化赖氨酸的特定肽的反应性。
从一名 RA 患者的标本中鉴定出对氨甲酰化但不对瓜氨酸化纤维蛋白原β链具有特异性反应的血清。LC-MS 鉴定出人纤维蛋白原β链中 34 个赖氨酸中有 9 个发生了氨甲酰化。免疫反应性图谱显示了几个候选氨甲酰化表位,这些表位通过竞争实验得到了证实。在一些 RA 患者血清中,含有第 83 位同型瓜氨酸的肽似乎是一个免疫优势表位,对含有第 52、264、351、367 和 374 位同型瓜氨酸的肽也有额外的反应性。
抗 CarP 抗体似乎优先靶向人纤维蛋白原β链中含有同型瓜氨酸的特定区域。有趣的是,在一些患者中,体液免疫反应性似乎相对受限,这可能使我们能够检测到与疾病表型的特定关系。