Nakabo Shuichiro, Hashimoto Motomu, Ito Shinji, Furu Moritoshi, Ito Hiromu, Fujii Takao, Yoshifuji Hajime, Imura Yoshitaka, Nakashima Ran, Murakami Kosaku, Kuramoto Nobuo, Tanaka Masao, Satoh Junko, Ishigami Akihito, Morita Satoshi, Mimori Tsuneyo, Ohmura Koichiro
Department of Rheumatology and Clinical Immunology.
Department of the Control for Rheumatic Diseases.
Rheumatology (Oxford). 2017 Jul 1;56(7):1217-1226. doi: 10.1093/rheumatology/kex088.
Anti-carbamylated protein (anti-CarP) antibodies are detected in RA patients. Fetal calf serum is used as an antigen source in anti-CarP ELISA, and the precise target antigens have not been found. We aimed to identify the target antigens of anti-CarP antibodies.
Western blotting of anti-CarP antibodies was conducted. Anti-carbamylated human albumin (CarALB) antibody was detected by in-house ELISA for 493 RA patients and 144 healthy controls (HCs). An inhibition ELISA of anti-CarP antibodies by CarALB and citrullinated albumin (citALB) was performed using eight RA patients' sera. Serum CarALB was detected by liquid chromatography-tandem mass spectroscopy (LC/MS/MS), and the serum MPO concentration was measured by ELISA.
We focused on carbamylated albumin because it corresponded to the size of the thickest band detected by western blotting of anti-CarP antibodies. Anti-CarALB antibody was detected in 31.4% of RA patients, and the correlation of the titres between anti-CarALB and anti-CarP was much closer than that between anti-citALB and anti-CCP antibodies (ρ = 0.59 and ρ = 0.16, respectively). The inhibition ELISA showed that anti-CarP antibodies were inhibited by CarALB, but not by citALB. CarALB was detected in sera from RA patients by LC/MS/MS. The serum MPO concentration was correlated with disease activity and was higher in RA patients with anti-CarALB antibody than in those without.
We found that carbamylated albumin is a novel target antigen of anti-CarP antibodies, and it is the first reported target antigen that has not been reported as the target of ACPA.
在类风湿关节炎(RA)患者中检测到抗氨甲酰化蛋白(anti-CarP)抗体。在抗CarP酶联免疫吸附测定(ELISA)中,胎牛血清用作抗原来源,尚未发现确切的靶抗原。我们旨在鉴定抗CarP抗体的靶抗原。
进行抗CarP抗体的蛋白质印迹分析。采用内部ELISA法检测493例RA患者和144例健康对照(HC)的抗氨甲酰化人白蛋白(CarALB)抗体。使用8例RA患者的血清进行CarALB和瓜氨酸化白蛋白(citALB)对抗CarP抗体的抑制ELISA。通过液相色谱-串联质谱(LC/MS/MS)检测血清CarALB,并采用ELISA法测定血清髓过氧化物酶(MPO)浓度。
我们关注氨甲酰化白蛋白,因为它与抗CarP抗体蛋白质印迹检测到的最粗条带大小相符。31.4%的RA患者检测到抗CarALB抗体,抗CarALB与抗CarP之间滴度的相关性比抗citALB与抗环瓜氨酸肽(CCP)抗体之间的相关性更密切(分别为ρ = 0.59和ρ = 0.16)。抑制ELISA显示,抗CarP抗体被CarALB抑制,但未被citALB抑制。通过LC/MS/MS在RA患者血清中检测到CarALB。血清MPO浓度与疾病活动相关,抗CarALB抗体阳性的RA患者血清MPO浓度高于阴性患者。
我们发现氨甲酰化白蛋白是抗CarP抗体的一种新型靶抗原,且是首个未被报道为抗环瓜氨酸肽抗体(ACPA)靶抗原的靶抗原。