Regulatory and other rheumatoid factors in rheumatoid arthritis patients with active disease or in remission
Background Previously, we identified a regulatory rheumatoid factor (regRF), the production of which provides rats with resistance to collagen‐induced arthritis (CIA). Immunization with conformers of IgG Fc fragments carrying epitopes specific to regRF reduces symptoms of CIA. The aim of this study...
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Published in | Journal of clinical laboratory analysis Vol. 36; no. 2; pp. e24187 - n/a |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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John Wiley & Sons, Inc
01.02.2022
John Wiley and Sons Inc |
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Abstract | Background
Previously, we identified a regulatory rheumatoid factor (regRF), the production of which provides rats with resistance to collagen‐induced arthritis (CIA). Immunization with conformers of IgG Fc fragments carrying epitopes specific to regRF reduces symptoms of CIA. The aim of this study was to determine whether there is a link between regRF levels and rheumatoid arthritis (RA) activity in humans in order to assess the potential of regRF as a therapeutic biotarget in RA. The variability of rheumatoid factor (RF) specificities present in the blood of RA patients was also studied.
Methods
The regRF were studied in RA patients with active disease and in remission. Variability in the specificities of RF associated with RA was studied by concurrent inhibition of RF latex fixation by variants of modified IgG.
Results
Patients in remission had regRF levels higher than in healthy subjects. The regRF in remission was characterized by tight binding to its antigen, as in healthy subjects. The regRF levels in patients with active RA varied dramatically, and regRF binding to its antigen was weak. The exacerbation of Still's disease coincided with low regRF levels and affinity, while an improvement in patient condition was associated with an increase in regRF levels and affinity. The RF specific to RA, which was detected by the RF latex‐fixation method, was a nonhomogeneous population of antibodies that included RF to lyophilized IgG, to IgG immobilized on polystyrene, and to rabbit IgG.
Conclusion
Stimulating regRF production might enable improved RA therapy.
Patients with active RA were found to have low regRF levels and affinity, while patients in remission had regRF levels higher than in healthy subjects, and the regRF was characterized by tight binding to its antigen. The exacerbation of Still's disease coincides with low regRF levels and affinity, while an improvement in condition is associated with an increase in regRF levels and affinity. The RF specific to RA, which is detected by the RF latex fixation method, is a nonhomogeneous population of antibodies that includes RF to lyophilized IgG, to IgG immobilized on polystyrene, and to rabbit IgG. |
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AbstractList | BackgroundPreviously, we identified a regulatory rheumatoid factor (regRF), the production of which provides rats with resistance to collagen‐induced arthritis (CIA). Immunization with conformers of IgG Fc fragments carrying epitopes specific to regRF reduces symptoms of CIA. The aim of this study was to determine whether there is a link between regRF levels and rheumatoid arthritis (RA) activity in humans in order to assess the potential of regRF as a therapeutic biotarget in RA. The variability of rheumatoid factor (RF) specificities present in the blood of RA patients was also studied.MethodsThe regRF were studied in RA patients with active disease and in remission. Variability in the specificities of RF associated with RA was studied by concurrent inhibition of RF latex fixation by variants of modified IgG.ResultsPatients in remission had regRF levels higher than in healthy subjects. The regRF in remission was characterized by tight binding to its antigen, as in healthy subjects. The regRF levels in patients with active RA varied dramatically, and regRF binding to its antigen was weak. The exacerbation of Still's disease coincided with low regRF levels and affinity, while an improvement in patient condition was associated with an increase in regRF levels and affinity. The RF specific to RA, which was detected by the RF latex‐fixation method, was a nonhomogeneous population of antibodies that included RF to lyophilized IgG, to IgG immobilized on polystyrene, and to rabbit IgG.ConclusionStimulating regRF production might enable improved RA therapy. Previously, we identified a regulatory rheumatoid factor (regRF), the production of which provides rats with resistance to collagen-induced arthritis (CIA). Immunization with conformers of IgG Fc fragments carrying epitopes specific to regRF reduces symptoms of CIA. The aim of this study was to determine whether there is a link between regRF levels and rheumatoid arthritis (RA) activity in humans in order to assess the potential of regRF as a therapeutic biotarget in RA. The variability of rheumatoid factor (RF) specificities present in the blood of RA patients was also studied. The regRF were studied in RA patients with active disease and in remission. Variability in the specificities of RF associated with RA was studied by concurrent inhibition of RF latex fixation by variants of modified IgG. Patients in remission had regRF levels higher than in healthy subjects. The regRF in remission was characterized by tight binding to its antigen, as in healthy subjects. The regRF levels in patients with active RA varied dramatically, and regRF binding to its antigen was weak. The exacerbation of Still's disease coincided with low regRF levels and affinity, while an improvement in patient condition was associated with an increase in regRF levels and affinity. The RF specific to RA, which was detected by the RF latex-fixation method, was a nonhomogeneous population of antibodies that included RF to lyophilized IgG, to IgG immobilized on polystyrene, and to rabbit IgG. Stimulating regRF production might enable improved RA therapy. Previously, we identified a regulatory rheumatoid factor (regRF), the production of which provides rats with resistance to collagen-induced arthritis (CIA). Immunization with conformers of IgG Fc fragments carrying epitopes specific to regRF reduces symptoms of CIA. The aim of this study was to determine whether there is a link between regRF levels and rheumatoid arthritis (RA) activity in humans in order to assess the potential of regRF as a therapeutic biotarget in RA. The variability of rheumatoid factor (RF) specificities present in the blood of RA patients was also studied.BACKGROUNDPreviously, we identified a regulatory rheumatoid factor (regRF), the production of which provides rats with resistance to collagen-induced arthritis (CIA). Immunization with conformers of IgG Fc fragments carrying epitopes specific to regRF reduces symptoms of CIA. The aim of this study was to determine whether there is a link between regRF levels and rheumatoid arthritis (RA) activity in humans in order to assess the potential of regRF as a therapeutic biotarget in RA. The variability of rheumatoid factor (RF) specificities present in the blood of RA patients was also studied.The regRF were studied in RA patients with active disease and in remission. Variability in the specificities of RF associated with RA was studied by concurrent inhibition of RF latex fixation by variants of modified IgG.METHODSThe regRF were studied in RA patients with active disease and in remission. Variability in the specificities of RF associated with RA was studied by concurrent inhibition of RF latex fixation by variants of modified IgG.Patients in remission had regRF levels higher than in healthy subjects. The regRF in remission was characterized by tight binding to its antigen, as in healthy subjects. The regRF levels in patients with active RA varied dramatically, and regRF binding to its antigen was weak. The exacerbation of Still's disease coincided with low regRF levels and affinity, while an improvement in patient condition was associated with an increase in regRF levels and affinity. The RF specific to RA, which was detected by the RF latex-fixation method, was a nonhomogeneous population of antibodies that included RF to lyophilized IgG, to IgG immobilized on polystyrene, and to rabbit IgG.RESULTSPatients in remission had regRF levels higher than in healthy subjects. The regRF in remission was characterized by tight binding to its antigen, as in healthy subjects. The regRF levels in patients with active RA varied dramatically, and regRF binding to its antigen was weak. The exacerbation of Still's disease coincided with low regRF levels and affinity, while an improvement in patient condition was associated with an increase in regRF levels and affinity. The RF specific to RA, which was detected by the RF latex-fixation method, was a nonhomogeneous population of antibodies that included RF to lyophilized IgG, to IgG immobilized on polystyrene, and to rabbit IgG.Stimulating regRF production might enable improved RA therapy.CONCLUSIONStimulating regRF production might enable improved RA therapy. Background Previously, we identified a regulatory rheumatoid factor (regRF), the production of which provides rats with resistance to collagen‐induced arthritis (CIA). Immunization with conformers of IgG Fc fragments carrying epitopes specific to regRF reduces symptoms of CIA. The aim of this study was to determine whether there is a link between regRF levels and rheumatoid arthritis (RA) activity in humans in order to assess the potential of regRF as a therapeutic biotarget in RA. The variability of rheumatoid factor (RF) specificities present in the blood of RA patients was also studied. Methods The regRF were studied in RA patients with active disease and in remission. Variability in the specificities of RF associated with RA was studied by concurrent inhibition of RF latex fixation by variants of modified IgG. Results Patients in remission had regRF levels higher than in healthy subjects. The regRF in remission was characterized by tight binding to its antigen, as in healthy subjects. The regRF levels in patients with active RA varied dramatically, and regRF binding to its antigen was weak. The exacerbation of Still's disease coincided with low regRF levels and affinity, while an improvement in patient condition was associated with an increase in regRF levels and affinity. The RF specific to RA, which was detected by the RF latex‐fixation method, was a nonhomogeneous population of antibodies that included RF to lyophilized IgG, to IgG immobilized on polystyrene, and to rabbit IgG. Conclusion Stimulating regRF production might enable improved RA therapy. Patients with active RA were found to have low regRF levels and affinity, while patients in remission had regRF levels higher than in healthy subjects, and the regRF was characterized by tight binding to its antigen. The exacerbation of Still's disease coincides with low regRF levels and affinity, while an improvement in condition is associated with an increase in regRF levels and affinity. The RF specific to RA, which is detected by the RF latex fixation method, is a nonhomogeneous population of antibodies that includes RF to lyophilized IgG, to IgG immobilized on polystyrene, and to rabbit IgG. Patients with active RA were found to have low regRF levels and affinity, while patients in remission had regRF levels higher than in healthy subjects, and the regRF was characterized by tight binding to its antigen. The exacerbation of Still's disease coincides with low regRF levels and affinity, while an improvement in condition is associated with an increase in regRF levels and affinity. The RF specific to RA, which is detected by the RF latex fixation method, is a nonhomogeneous population of antibodies that includes RF to lyophilized IgG, to IgG immobilized on polystyrene, and to rabbit IgG. |
Author | Menshikov, Igor Beduleva, Liubov Menshikova, Daria Sidorov, Alexandr Semenova, Kseniya Khramova, Tatyana Khokhlova, Zhanna |
AuthorAffiliation | 1 Laboratory of Molecular and Cell Immunology Department of Immunology and Cell Biology Udmurt State University Izhevsk Russian Federation 3 Rezhevskaya Central Regional Hospital Rezh Russian Federation 4 Peoples’ Friendship University of Russia (RUDN University) Moscow Russian Federation 2 Laboratory of Biocompatible Materials Udmurt Federal Research Center UB RAS Izhevsk Russian Federation |
AuthorAffiliation_xml | – name: 3 Rezhevskaya Central Regional Hospital Rezh Russian Federation – name: 4 Peoples’ Friendship University of Russia (RUDN University) Moscow Russian Federation – name: 1 Laboratory of Molecular and Cell Immunology Department of Immunology and Cell Biology Udmurt State University Izhevsk Russian Federation – name: 2 Laboratory of Biocompatible Materials Udmurt Federal Research Center UB RAS Izhevsk Russian Federation |
Author_xml | – sequence: 1 givenname: Liubov orcidid: 0000-0002-2515-5960 surname: Beduleva fullname: Beduleva, Liubov email: blv76@mail.ru organization: Udmurt Federal Research Center UB RAS – sequence: 2 givenname: Alexandr orcidid: 0000-0003-3803-7493 surname: Sidorov fullname: Sidorov, Alexandr organization: Udmurt Federal Research Center UB RAS – sequence: 3 givenname: Kseniya orcidid: 0000-0001-5407-9517 surname: Semenova fullname: Semenova, Kseniya organization: Rezhevskaya Central Regional Hospital – sequence: 4 givenname: Zhanna orcidid: 0000-0003-4217-2911 surname: Khokhlova fullname: Khokhlova, Zhanna organization: Rezhevskaya Central Regional Hospital – sequence: 5 givenname: Daria orcidid: 0000-0001-8642-1209 surname: Menshikova fullname: Menshikova, Daria organization: Peoples’ Friendship University of Russia (RUDN University) – sequence: 6 givenname: Tatyana orcidid: 0000-0001-8401-3527 surname: Khramova fullname: Khramova, Tatyana organization: Udmurt Federal Research Center UB RAS – sequence: 7 givenname: Igor orcidid: 0000-0002-2221-7767 surname: Menshikov fullname: Menshikov, Igor organization: Udmurt Federal Research Center UB RAS |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/34952993$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1016/j.ijbiomac.2016.10.081 10.1002/jcla.23533 10.1002/art.30129 10.1016/j.imbio.2009.12.001 10.1111/1756-185X.12335 10.1371/journal.pone.0217624 10.1046/j.1365-2249.2001.01475.x 10.1016/B978-044482807-1/50015-6 10.1111/j.1749-6632.1986.tb20860.x 10.2174/1871530318666180308123350 |
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Keywords | pathological rheumatoid factor disease activity regulatory rheumatoid factor rheumatoid arthritis |
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Snippet | Background
Previously, we identified a regulatory rheumatoid factor (regRF), the production of which provides rats with resistance to collagen‐induced... Previously, we identified a regulatory rheumatoid factor (regRF), the production of which provides rats with resistance to collagen-induced arthritis (CIA).... BackgroundPreviously, we identified a regulatory rheumatoid factor (regRF), the production of which provides rats with resistance to collagen‐induced arthritis... Patients with active RA were found to have low regRF levels and affinity, while patients in remission had regRF levels higher than in healthy subjects, and the... |
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SubjectTerms | Adult Affinity Animals Arthritis, Rheumatoid - blood Arthritis, Rheumatoid - drug therapy Blood transfusions Collagen Disease disease activity Encephalomyelitis Epitopes Female Human subjects Humans Immunization Immunoglobulin G Immunoglobulin G - metabolism Juvenile rheumatoid arthritis Latex Lymphocytes - metabolism Male Medical research pathological rheumatoid factor Patients Polystyrene Rabbits regulatory rheumatoid factor Remission Remission (Medicine) Remission Induction Rheumatoid arthritis Rheumatoid factor Rheumatoid Factor - blood Rheumatoid Factor - metabolism Steroids Still's Disease, Adult-Onset - blood |
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Title | Regulatory and other rheumatoid factors in rheumatoid arthritis patients with active disease or in remission |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjcla.24187 https://www.ncbi.nlm.nih.gov/pubmed/34952993 https://www.proquest.com/docview/2628210199 https://www.proquest.com/docview/2614236176 https://pubmed.ncbi.nlm.nih.gov/PMC8841179 |
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