Journal of Peking University (Health Sciences) ›› 2023, Vol. 55 ›› Issue (4): 631-635. doi: 10.19723/j.issn.1671-167X.2023.04.010

Previous Articles     Next Articles

Significance of IgA isotype of anti-v-raf murine sarcoma viral oncogene homologue B1 antibody in rheumatoid arthritis

Yin-ji JIN,Lin SUN,Jin-xia ZHAO*(),Xiang-yuan LIU   

  1. Department of Rheumatology and Immunology, Peking University Third Hospital, Beijing 100191, China
  • Received:2020-07-31 Online:2023-08-18 Published:2023-08-03
  • Contact: Jin-xia ZHAO E-mail:zhao-jinxia@163.com
  • Supported by:
    the National Natural Science Foundation of China(81273293);the Seed Foundation of Peking University Third hospital(Y87473-01)

Abstract:

Objective: To detect serum IgA isotype of anti-v-raf murine sarcoma viral oncogene homologue B1 (BRAF) antibody levels in the rheumatoid arthritis (RA) patients in order to investigate their clinical significance in RA. Methods: Serum samples were obtained from 61 RA patients, 21 osteoarthritis (OA) patients, 16 systemic lupus erythematosus (SLE) patients, 16 gout patients, 16 Sjögren's syndrome (SS) patients and 22 healthy controls. IgA isotype of anti-BRAF antibody levels in the sera were examined by enzyme-linked immunosorbent assay (ELISA). The associations between IgA isotype of anti-BRAF antibody levels and the clinical features including age, disease duration and laboratory parameters including erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), rheumatoid factor (RF), disease activity score in 28 joints (DAS28), anti-cyclic citrullinated peptide (anti-CCP) antibody, immunoglobulin and BRAF protein levels in the RA patients were evaluated. Data analyses were performed by using SPSS 19.0 program. Results: The serum IgA isotype of anti-BRAF antibody levels in the RA patients were significantly higher than in the SLE, gout, OA patients and healthy controls, the P value was 0.011, < 0.001, < 0.001 and < 0.001, respectively. The serum IgA isotype of anti-BRAF antibody levels in the SS patients were also significantly higher than in the SLE, gout, OA patients and healthy controls, the P value was 0.029, 0.004, 0.001 and < 0.001, respectively. However, there was no difference between the RA and SS patients (P=0.762). IgA isotype of anti-BRAF antibody was measurable in the RA patients without RF, anti-CCP antibody or anti-keratin antibody (AKA) antibodies. The levels of IgA isotype of anti-BRAF antibody in the RA patients did not show any correlation with clinical features such as age and disease duration or laboratory parameters including ESR, CRP, RF, DAS28, anti-CCP antibody, immunoglobulin and BRAF protein levels. Compared with the clinical features and laboratory indexes of normal and elevated levels of IgA isotype of anti-BRAF antibody groups in the RA patients, there was no significant differences between the two groups in age, disease duration, ESR, CRP, RF, DAS28, anti-CCP antibody, immunoglobulin or BRAF protein levels. Conclusion: The elevated level of IgA isotype of anti-BRAF antibody in the RA patients showed that IgA isotype of anti-BRAF antibody might play a role in the pathogenesis of RA. Furthermore, detection of IgA isotype of anti-BRAF antibody in the serum negative RA patients showed that it might be helpful for the diagnosis of the serum negative RA patients.

Key words: Rheumatoid arthritis, v-raf murine sarcoma viral oncogene homologue B1, IgA isotype of anti-BRAF antibody

CLC Number: 

  • R593.22

Table 1

The AU level of IgA isotype of anti-BRAF antibody in different disease groups"

Disease type n AU P value
RA 61 62.4±43.5
SS 16 65.6±35.6 0.762
SLE 16 37.0±21.3 0.011
Gout 16 29.1±22.9 < 0.001
OA 21 21.9±17.2 < 0.001
Normal control 22 15.2±22.0 < 0.001

Table 2

Correlation analysis between the level of IgA isotype of anti-BRAF antibody and laboratory indexes in the RA patients"

Clinical index Correlation coefficient P value
Age -0.026 0.858
Duration 0.253 0.079
DAS28 -0.048 0.760
CRP 0.010 0.946
ESR 0.088 0.555
RF 0.207 0.153
Anti-CCP 0.053 1.725
IgA 0.143 0.419
IgM 0.129 0.469
IgG -0.088 0.614
BRAF protein 0.153 0.292

Table 3

Comparison of laboratory indexes of positive and negative IgA isotype of anti-BRAF antibody in RA patients"

Clinical index Antibody positive group Antibody negative group P value
Age/years 53.4±13.5 52.6±15.9 0.848
Duration/months 60.0 (1.0-360.0) 33.0 (1.0-240.0) 0.335
DAS28 4.56±1.27 4.60±0.62 0.879
CRP/(mg/dL) 2.11 (0.11-16.60) 2.58 (0.11-8.89) 0.818
ESR/(mm/h) 41.5 (2.0-110.0) 42.0 (6.0-84.0) 0.907
RF/(IU/mL) 115.0 (10.0-1 860.0) 50.0 (10.0-1 890.0) 0.126
Anti-CCP/(U/mL) 135.0 (7.0-500.0) 100.0 (7.0-500.0) 1.003
IgA/(mg/L) 3 340±1 340 3 340±1 610 0.719
IgM/(mg/L) 1 140 (610-3 990) 1 130 (210-2 640) 0.885
IgG/(mg/L) 15 440±6 700 17 680±7 850 0.371
BRAF protein/(ng/L) 9 557.5±8 208.9 6 865.6±5 368.4 0.196
1 Ikawa S , Fukui M , Ueyama Y , et al. B-raf, a new member of the raf family is activated by DNA rearrangement[J]. Mol Cell Biol, 1988, 8 (6): 2651- 2654.
2 Karhryn I . Raf protiens and cancer: B-Raf is identified as a mutational target[J]. Biochim Biophys Acta, 2003, 1653 (1): 25- 40.
3 Luo SF , Fang RY , Hsieh HL , et al. Involvement of MAPKs and NF-kappaB in tumor necrosis factor alpha-induced vascular cell adhesion molecule l expression in human rheumatoid arthritis synovial fibroblasts[J]. Arthritis Rheum, 2010, 62 (1): 105- 116.
doi: 10.1002/art.25060
4 Schett G , Zwerina J , Firestein G . The p38 mitogen-activated protein kinase (MAPK) pathway in rheumatoid arthritis[J]. Ann Rheum Dis, 2008, 67 (7): 909- 916.
doi: 10.1136/ard.2007.074278
5 Auger I , Balandraud N , Rak J , et al. New autoantigens in rheumatoid arthritis (RA): Screening 8268 protein arrays with sera from patients with RA[J]. Ann Rheum Dis, 2009, 68 (4): 591- 594.
doi: 10.1136/ard.2008.096917
6 Szekanecz Z , Soós L , Szabó Z , et al. Anti-citrullinated protein antibodies in rheumatoid arthritis: As good as it gets?[J]. Clin Rev Allergy Immunol, 2008, 34 (1): 26- 31.
doi: 10.1007/s12016-007-8022-5
7 Wang XP , Cheng QY , Gu MM , et al. Diagnostic accuracy of anti-keratin antibody for rheumatoid arthritis: A meta-analysis[J]. Clin Rheumatol, 2019, 38 (7): 1841- 1849.
doi: 10.1007/s10067-019-04464-x
8 Charpin C , Martin M , Balandraud N , et al. Autoantibodies to BRAF, a new family of autoantibodies associated with rheumatoid arthritis[J]. Arthritis Res Ther, 2010, 12 (5): R194.
doi: 10.1186/ar3165
9 张霞, 赵金霞, 孙琳, 等. 抗鼠科肉瘤病毒癌基因同源物B1抗体的检测及其在类风湿关节炎诊断中的意义[J]. 北京大学学报(医学版), 2012, 44 (2): 195- 198.
10 Woof JM , Mestecky J . Mucosal immunoglobulins[J]. Immunol Rev, 2005, 206, 64- 82.
doi: 10.1111/j.0105-2896.2005.00290.x
11 Thalhamer T , McGrath MA , Hamett MM . MAPKs and their relevance to arthritis and inflammation[J]. Rheumatology (Oxford), 2008, 47 (4): 409- 414.
[1] Wen-xin CAI,Shi-cheng LI,Yi-ming LIU,Ru-yu LIANG,Jing LI,Jian-ping GUO,Fan-lei HU,Xiao-lin SUN,Chun LI,Xu LIU,Hua YE,Li-zong DENG,Ru LI,Zhan-guo LI. A cross-sectional study on the clinical phenotypes of rheumatoid arthritis [J]. Journal of Peking University (Health Sciences), 2022, 54(6): 1068-1073.
[2] Fang CHENG,Shao-ying YANG,Xing-xing FANG,Xuan WANG,Fu-tao ZHAO. Role of the CCL28-CCR10 pathway in monocyte migration in rheumatoid arthritis [J]. Journal of Peking University (Health Sciences), 2022, 54(6): 1074-1078.
[3] Rui LIU,Jin-xia ZHAO,Liang YAN. Clinical characteristics of patients with rheumatoid arthritis complicated with venous thrombosis of lower extremities [J]. Journal of Peking University (Health Sciences), 2022, 54(6): 1079-1085.
[4] Jing-feng ZHANG,Yin-ji JIN,Hui WEI,Zhong-qiang YAO,Jin-xia ZHAO. Cross-sectional study on quality of life and disease activity of rheumatoid arthritis patients [J]. Journal of Peking University (Health Sciences), 2022, 54(6): 1086-1093.
[5] GAO Chao,CHEN Li-hong,WANG Li,YAO Hong,HUANG Xiao-wei,JIA Yu-bo,LIU Tian. Validation of the Pollard’s classification criteria (2010) for rheumatoid arthritis patients with fibromyalgia [J]. Journal of Peking University (Health Sciences), 2022, 54(2): 278-282.
[6] LOU Xue,LIAO Li,LI Xing-jun,WANG Nan,LIU Shuang,CUI Ruo-mei,XU Jian. Methylation status and expression of TWEAK gene promoter region in peripheral blood of patients with rheumatoid arthritis [J]. Journal of Peking University (Health Sciences), 2021, 53(6): 1020-1025.
[7] ZHONG Hua,XU Li-ling,BAI Ming-xin,SU Yin. Effect of chemokines CXCL9 and CXCL10 on bone erosion in patients with rheumatoid arthritis [J]. Journal of Peking University (Health Sciences), 2021, 53(6): 1026-1031.
[8] LUO Liang,HUO Wen-gang,ZHANG Qin,LI Chun. Clinical characteristics and risk factors of rheumatoid arthritis with ulcerative keratitis [J]. Journal of Peking University (Health Sciences), 2021, 53(6): 1032-1036.
[9] ZHANG Lu,HU Xiao-hong,CHEN Cheng,CAI Yue-ming,WANG Qing-wen,ZHAO Jin-xia. Analysis of cervical instability and clinical characteristics in treatment-naive rheumatoid arthritis patients [J]. Journal of Peking University (Health Sciences), 2021, 53(6): 1049-1054.
[10] CAO Di,WANG Yan,WANG Liu-qing,SUN Xiao-lin,HUANG Fei,MENG Yang,REN Li-li,ZHANG Xue-wu. Expression of plasma Dickkopf-1 in patients with rheumatoid arthritis and its correlation with peripheral blood T cell subsets [J]. Journal of Peking University (Health Sciences), 2021, 53(2): 255-260.
[11] ZHAO Kai,CHANG Zhi-fang,WANG Zhi-hua,PANG Chun-yan,WANG Yong-fu. Therapeutic effect of gene silencing peptidyl arginine deaminase 4 on pulmonary interstitial lesions induced by collagen-induced arthritis mice [J]. Journal of Peking University (Health Sciences), 2021, 53(2): 235-239.
[12] Jia-jing PENG,Tian LIU. Rheumatoid arthritis combined with pigmented villonodular synovitis: A case report and literature review [J]. Journal of Peking University (Health Sciences), 2020, 52(6): 1135-1139.
[13] Jia-li CHEN,Yue-bo JIN,Yi-fan WANG,Xiao-ying ZHANG,Jing LI,Hai-hong YAO,Jing HE,Chun LI. Clinical characteristics and risk factors of cardiovascular disease in patients with elderly-onset rheumatoid arthritis: A large cross-sectional clinical study [J]. Journal of Peking University (Health Sciences), 2020, 52(6): 1040-1047.
[14] Lu ZHANG,Xiao-hong HU,Qing-wen WANG,Yue-ming CAI,Jin-xia ZHAO,Xiang-yuan LIU. Population distribution and clinical characteristics in rheumatoid arthritis patients with cervical spine instability [J]. Journal of Peking University (Health Sciences), 2020, 52(6): 1034-1039.
[15] Guo TANG,Li LONG,Ya-xin HAN,Qing PENG,Jia-jun LIU,Hua SHANG. Clinical characteristics and related factors of rheumatoid arthritis complicated with tuberculosis infection [J]. Journal of Peking University (Health Sciences), 2020, 52(6): 1029-1033.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!