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Updated: Jun 17, 2026

Antibody Binding Specificity for Kappa (Vκ) Light Chain-containing Human (IgM) Antibodies: Polysialic Acid (PSA) Attached to NCAM as a Case Study
Published on: June 29, 2016
Antibodies targeting mutated citrullinated vimentin in patients with psoriatic arthritis
Andrea Tesija-Kuna1, Simeon Grazio, Marijana Miler
1University Department of Chemistry, Sestre Milosrdnice University Hospital, Vinogradska 29, 10000, Zagreb, Croatia. andrea.kuna@gmail.com
Abstract:
Antibodies against mutated citrullinated vimentin (anti-MCV) are of a comparable diagnostic value in rheumatoid arthritis (RA) as antibodies targeting citrullinated peptides (anti-CCP). Anti-CCP are present in up to 15% of psoriatic arthritis (PsA) patients, while the prevalence of anti-MCV in PsA patients has been poorly investigated. The aim of the present study was to assess the prevalence and relevance of anti-MCV antibodies in PsA patients. The study included 56 PsA patients. Clinical features, disease activity, and functional ability were noted by an experienced rheumatologist. Serum samples of all patients were analyzed for anti-MCV and anti-CCP antibodies using enzyme-linked immunosorbent assay. Data on 92 patients with RA, 44 patients with other inflammatory rheumatic diseases, and 107 healthy controls from a previous study were used to compare the prevalence of anti-MCV antibodies in PsA patients. Anti-MCV antibodies were positive in only two out of 56 (3.6%) PsA patients, which was significantly lower compared to RA patients (63%). The anti-MCV level was moderately positive and borderline in one patient each. Both patients had asymmetric polyarthritis, dactylitis, moderate to high disease activity, and were anti-CCP and rheumatoid factor (RF) negative. There was no significant difference in anti-MCV levels according to clinical subtypes of PsA and no correlation of anti-MCV levels with anti-CCP, RF, disease activity variables, and functional ability indices. According to study results, anti-MCV antibodies can be detected in a very small proportion of PsA patients with polyarthritic disease and are primarily related to the polyarthritic pattern rather than the specific diagnosis of RA.
Insights
Antibodies against mutated citrullinated vimentin (anti-MCV) are rarely found in psoriatic arthritis (PsA) patients, unlike in rheumatoid arthritis (RA). This study found anti-MCV in only 3.6% of PsA patients, suggesting limited diagnostic utility for PsA.
Area of Science:
- Immunology
- Rheumatology
- Clinical Diagnostics
Background:
- Antibodies against mutated citrullinated vimentin (anti-MCV) and antibodies against citrullinated peptides (anti-CCP) are key biomarkers for rheumatoid arthritis (RA).
- While anti-CCP antibodies are found in some psoriatic arthritis (PsA) patients, the prevalence and significance of anti-MCV antibodies in PsA remain largely uninvestigated.
Purpose of the Study:
- To determine the prevalence and clinical relevance of anti-MCV antibodies in patients diagnosed with psoriatic arthritis (PsA).
Main Methods:
- Enzyme-linked immunosorbent assay (ELISA) was used to analyze serum samples from 56 PsA patients for anti-MCV and anti-CCP antibodies.
- Clinical data, disease activity, and functional status were recorded by a rheumatologist.
- Prevalence data were compared with those from a previous study including RA patients, other inflammatory rheumatic diseases, and healthy controls.
Main Results:
- Anti-MCV antibodies were detected in only 2 out of 56 (3.6%) PsA patients, a significantly lower prevalence compared to RA patients (63%).
- The positive cases exhibited asymmetric polyarthritis, dactylitis, moderate to high disease activity, and were negative for anti-CCP and rheumatoid factor (RF).
- No significant association was found between anti-MCV levels and PsA clinical subtypes, anti-CCP, RF, disease activity, or functional indices.
Conclusions:
- Anti-MCV antibodies are present in a very small subset of PsA patients, primarily those with a polyarthritic presentation.
- The findings suggest that anti-MCV antibodies are not a significant diagnostic marker for PsA and their presence may be related to polyarthritic patterns rather than a specific diagnosis of RA.
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