Evidence map›Paper›PMID 39872186›Full record

ArticleMedical journal, Armed Forces India

An observational study to determine the role of indirect immunofluorescence and ELISA for desmogleins in the diagnosis and monitoring of autoimmune bullous disorders.

Veena Kharayat, Biju Vasudevan, K Lekshmi Priya, Rajesh Verma, Prabal Deb, M S Deora

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Article in Medical journal, Armed Forces India. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Veena KharayatAssistant Professor (Dermatology), Military Hospital Jabalpur, India.
Biju VasudevanProfessor & Head, Department of Dermatology, Armed Forces Medical College, Pune, India.
K Lekshmi PriyaAssistant Professor, Department of Dermatology, Armed Forces Medical College, Pune, India.
Rajesh VermaMG (Med), HQ UB Area, Bareilly, India.
Prabal DebChief Operating Officer & Chief Histopathologist, NM Medical, Mumbai, India.
M S DeoraProfessor & Head (Dermatology), DY Patil Medical College & Research Centre, Pune, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Autoimmune bullous disorder (AIBD) is a diverse group of blistering dermatoses that affects the skin and mucous membrane, characterized by the formation of autoantibodies against the desmosomal glycoproteins and adhesion molecular components of the basement membrane zone. Various immunoassay techniques for serological diagnosis are Direct Immunofluorescence (DIF), Indirect Immunofluorescence (IIF), Enzyme Linked Immunosorbent Assay (ELISA) and immunoblotting. Quantitative ELISA titer can also be used to monitor the disease activity and response to treatment. The aim of this study was to evaluate the role of IIF in diagnosing various AIBDs and the role of ELISA for desmogleins in monitoring disease activity in the pemphigus group of disorders. Methods: A total of 45 patients with freshly diagnosed AIBD were included in the study. Skin biopsies were done to establish the diagnosis by histopathology and DIF. BIOCHIP-based IIF assay was performed on the sera of the patient. The sensitivity and specificity of the IIF assay were then calculated based on the established diagnosis by Histopathological examination (HPE) and DIF. Quantitative ELISA titer was performed to measure the antibody (anti desmoglein (Dsg) 1 and 3) titre in serum samples of patients with pemphigus at baseline, 1 and 3 months follow-up after initiation of appropriate treatment therapy and results were then compared with disease activity scoring system. Results: Sensitivity and specificity of IIF for Dsg 1 for the pemphigus group were derived to be 85.7% and 98.2% respectively, while that for Dsg 3 were 100% and 98.7%, respectively. Sensitivity (90-100%) of IIF for Bullous pemphigoid was higher than specificity (85-96%). The ELISA titers of anti Dsg1 and 3 were also observed to fall sequentially so was the disease activity score during the follow-up visits at 1 and 3 months. Conclusion: Biochip IIF assay can be used as a screening tool for the serological diagnosis of AIBD and quantitative ELISA for monitoring the disease activity and response to treatment.

Indexed as

Autoimmune bullous disorderBIOCHIPELISAImmunofluorescenceSensitivitySpecificity

Identifiers

PMID39872186
PMCPMC11763186

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