scholarly journals Occurrence of nucleic acid hydrolyzing IgM antibodies in rheumatoid arthritis patients’ sera

2020 ◽  
Vol 4 (1) ◽  
Author(s):  
Ramesh Rajendran ◽  
Prabu Charan E ◽  
Kamalanathan A S
2011 ◽  
Vol 89 (9) ◽  
pp. 675-862 ◽  
Author(s):  
Lenesha Warrener ◽  
Rimantas Slibinskas ◽  
Kaw Bing Chua ◽  
Wondatir Nigatu ◽  
Kevin Brown ◽  
...  

2009 ◽  
Vol 36 (5) ◽  
pp. 893-897 ◽  
Author(s):  
BARBARA J. ROSENAU ◽  
PETER H. SCHUR

Objective.Rheumatoid arthritis (RA) is a chronic inflammatory polyarthritis; while the cause is unknown, it has been speculated that an infectious agent could be the trigger for the disease. Numerous attempts at isolating an agent have been unsuccessful. Our purpose was to identify a virus from diseased tissue from a patient with RA.Methods.Diseased tissue taken at the time of knee replacement surgery from a patient with RA was inoculated into several cell lines and observed for cytopathic effect. Cells from the tissue were also grown as explants and were examined for viruses. Synovial fluid drawn 4 years prior to the surgery and frozen at −70°C was also inoculated into cell lines. Following the development of a cytopathic effect and identification of the agent, sera from 50 patients with rheumatoid factor (RF)-negative RA were examined for IgM antibodies to the agent.Results.After many inoculations and numerous subpassages, measles virus was identified in 6 cell lines inoculated with either the minced tissue or synovial fluid. Six cell lines co-cultivated with one or more of 9 explants also showed the presence of measles virus. Measles virus was confirmed by immunofluorescence and by neutralization. Eleven of 50 (22%) sera samples from patients with RF-negative RA had IgM antibodies to measles virus recombinant nucleoprotein.Conclusion.There is an association between measles virus and RA.


2010 ◽  
Vol 23 (6) ◽  
pp. 577-582 ◽  
Author(s):  
A. S. Kamalanathan ◽  
C. Goulvestre ◽  
B. Weill ◽  
M. A. Vijayalakshmi

2016 ◽  
Vol 170 ◽  
pp. 27-36 ◽  
Author(s):  
Tue G. Nguyen ◽  
Kelly J. McKelvey ◽  
Lyn M. March ◽  
David J. Hunter ◽  
Meilang Xue ◽  
...  

2013 ◽  
Vol 7 (1) ◽  
pp. 75-80 ◽  
Author(s):  
Maurizio Benucci ◽  
Gianantonio Saviola ◽  
Francesca Meacci ◽  
Mariangela Manfredi ◽  
Maria Infantino ◽  
...  

The use of tumour necrosis factor (TNF) antagonists (infliximab [IFN], etanercept [ETN], adalimumab [ADA]) has changed the course of many rheumatic diseases, including rheumatoid arthritis (RA). However, some questions concerning their safety have emerged since their approval because they can trigger immunisation, induce rare type I and III hypersensitivity, and cause acute and delayed reactions. The aim of this study was to evaluate the correlations between hypersensitivity reactions to biological agents, disease activity and the development of class-specific IgA and IgM antibodies against the three anti-TNF agents in patients with RA. This longitudinal observational study involved consecutive outpatients with active RA who started treatment with IFN (n=30), ETN (n=41) or ADA (n=28). Clinical data and systemic and local side effects were collected prospectively at baseline and after six months of anti-TNF treatment. Serum samples were taken at the same time points in order to measure antibodies against the TNF blockers, anti-nuclear (ANA) and anti-dsDNA antibodies. The IgA and IgM antibodies specific to all three anti-TNF-α agents were analysed using ImmunoCaP Phadia- Thermofisher especially developed in collaboration with the laboratory of Immunology and Allergy, San Giovanni di Dio, Florence. The mean age of the 99 patients (86% females) was 54.6±12.4 years, and the median disease duration was 11.2±.3.2 years (range 3-14.3). The three treatment groups were comparable in terms of age, gender, rheumatoid factor and anti-citrullinated peptide (CCP) antibody positivity, and baseline C-reactive protein levels, erythrocyte sedimentation rate, 28-joint disease activity scores, and concomitant medications. Twelve patients treated with INF (40%) had anti-IFN IgM, and two (6%) anti-IFN IgA; 19 patients treated with ADA (68%) had anti-ADA IgM, and four (6%) anti-ADA IgA; and 27 patients treated with ETN (66%) had anti-ETN IgM, and 24 (58%) anti-ETN IgA. There were five systemic reactions in the IFN group, and seven adverse local reactions in both the ADA and the ETN group. There was no correlation between drug-specific IgA and IgM antibodies (p=0.65). There was also no correlation between the antibodies and disease activity after six months of treatment (r=0.189;p=0.32). Our findings show that the development of antibodies against IFN, ADA or ETN of IgA and IgM class are not related to any decrease in efficacy or early discontinuation of anti-TNF treatment in RA patients, nor to systemic and local reactions. Further studies of larger series of RA patients are needed to confirm the relationships between the development of drug-specific antibodies, serum TNF blocker levels, and disease activity.


2020 ◽  
Vol 79 (Suppl 1) ◽  
pp. 1343.1-1344
Author(s):  
N. Bashlakova ◽  
T. Tyabut ◽  
A. Buglova ◽  
A. Trushyna

Background:Currently, some data have been accumulated on the participation of antiphospholipid antibodies (aPL) in the development of thrombotic complications in patients with autoimmune rheumatic diseases (ARD), in particular, in patients with systemic lupus erythematosus (SLE). The most studied aPL in this pathology are IgG and IgM antibodies to cardiolipin (aCL), anti-β2-glycoprotein 1 antibodies (aβ2-GP 1), lupus anticoagulant (LA). The participation of IgG and IgM antibodies to prothrombin (aPT) and to annexin V (aAnV), antibodies to oxidized low density lipoproteins (aOxLDL) in hypercoagulation and the development of thrombosis is also discussed. However, the studies focusing on the investigation of aPL in patients with rheumatoid arthritis (RA) are few.Objectives:To estimate the levels and the frequency of occurrence of aPL in patients with RA in comparison to the SLE patients and the control group.Methods:The study included 85 female patients with ARD (RA (n=45), mean age 43,0 (33,0; 52,0) years old, disease duration 9,0 (5,0; 13,0) years, disease activity (DAS28= 5,37 (4,69; 5,89) points) and SLE (n=40), mean age 33,5 (27,5; 44,5) years old, disease duration 8,0 (5,0; 14,5) years, disease activity SLEDAI-2K 7,0 (4,0; 11,5) points). Fifty four healthy women (mean age 38,5 (35,0; 46,0) years old) formed the control group.The levels of antiphospholipid antibodies (IgG/IgM aCL, aβ2-GP 1, aAnV and aPT, aOxLDL) were determined with ELISA according to the instruction of a manufacturer. LA was determined by one-stage clotting assay using reagents for screening and confirmation (Technoclot LA Screen and Technoclot LA Confirm, Austria).Results:The frequency of occurrence of elevated levels of all investigated aPL in patients with RA was similar to SLE patients and was revealed in 57,8% of cases for IgG/IgM aCL, 44,4% for IgG/IgM aβ2-GP-1, 26,7% for IgG/IgM aAnV, 8,9% for aPT, 52,6% for LA, 64,4% for aOxLDL. The patients with SLE had an increased levels of IgG/IgM aCL in 60,0% of cases, IgG/IgM aβ2-GP-1 in 57,5%, IgG/IgM aAnV in 15,0%, IgG/IgM aPT in 17,5%, high levels of LA in 68,8%, of IgG aOxLDL – in 80,0% of cases. The control group had a high levels of IgG/IgM aCL in 1,8%, IgG/IgM aβ2-GP-1 in 3,7%, IgG/IgM aAnV in 5,6%, IgG/IgM aPT in 1,8%, high levels of IgG aOxLDL – in 42,6% of cases. None of the controls had an increased level of LA. The frequency of occurrence of elevated levels of aPL and their mean levels in both groups of patients with ARD was higher as compare to the control group (р<0,05).The mean levels of IgG aβ2-GP-1, LA, aOxLDL in SLE patients and mean levels of LA, aOxLDL in RA patients were above standard values but were similar in both groups. Moreover, the mean levels of IgG aCL, IgM aβ2-GP-1, IgG/IgM aAnV and aPT were comparable in patients with SLE and RA. However, the mean levels of IgM aCL in RA patients was higher than in SLE patients. This may indicate an increased autoimmune activity.Simultaneous elevation in four types of aPL levels was observed in 4,4% patients with RA, in 2,5% - with SLE; simultaneous elevation in three types of aPL was reveled in 11,1% patients with RA, in 17,5% - with SLE; two types of aPL were increased in 35,6% patients with RA and 27,5% - with SLE. Only one type of elevated aPL levels (12,9%) was indentified in the control group.Conclusion:Thus, patients with RA are characterized by a wide range of aPL. Qualitative and quantitative changes in the levels and types of autoantibodies in patients with RA have been established similar to those in SLE patients.In patients with autoimmune rheumatic pathology, the presence of simultaneously elevated several types of aPL have been proved.Disclosure of Interests:None declared


Sign in / Sign up

Export Citation Format

Share Document