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Laboratory Diagnosis of ANCA-Associated Vasculitis (AAV) Using a Combination of Immunofluorescence Test (IIFT) and Line Immunoassay (LIA): Single-Centre Report From India.
Chauhan, Rajni; Jain, Dharmendra; Tiwari, Aseem Kumar; Dorwal, Pranav; Raina, Vimarsh; Nandi, Shoma Paul.
Afiliação
  • Chauhan R; Molecular and Transplant Immunology Laboratory, Department of Transfusion Medicine, Medanta-The Medicity, Gurgaon, India; Amity Institute of Biotechnology, Amity University Uttar Pradesh, Noida, India.
  • Jain D; Molecular and Transplant Immunology Laboratory, Department of Transfusion Medicine, Medanta-The Medicity, Gurgaon, India.
  • Tiwari AK; Molecular and Transplant Immunology Laboratory, Department of Transfusion Medicine, Medanta-The Medicity, Gurgaon, India.
  • Dorwal P; Molecular and Transplant Immunology Laboratory, Department of Transfusion Medicine, Medanta-The Medicity, Gurgaon, India.
  • Raina V; Chimera Transplant Research Foundation, New Delhi, India.
  • Nandi SP; Amity Institute of Biotechnology, Amity University Uttar Pradesh, Noida, India. Electronic address: spaul@amity.edu.
Reumatol Clin (Engl Ed) ; 18(1): 15-19, 2022 Jan.
Article em En | MEDLINE | ID: mdl-35090607
ABSTRACT

INTRODUCTION:

Anti-neutrophil cytoplasmic autoantibodies (ANCA) associated vasculitis (AAV) is a small vessel vasculitis with insufficient epidemiological estimates in India. We aimed to determine demographic, clinical features, and laboratory diagnosis of AAV patients presenting to a large tertiary care centre in India. MATERIAL AND

METHODS:

1289 patient samples were screened for ANCA by indirect immunofluorescence test (IIFT) and confirmation of ANCA target antigens was done by line immunoassay. Association between IIFT and LIA was determined in AAV.

RESULTS:

By IIFT, ANCA was detected in 13.0% (168 out of 1289), of which 23.8% (40/168) were positive with P-ANCA pattern, 25.0% (42/168) were positive with C-ANCA and 47.6% (80/168) showed an atypical pattern. On evaluation with a line immunoassay, 6.7% (86/1289) were positive out of which 52.3% (45/86), 41.9% (36/86), 8.8% (6/86) were positive for anti-MPO, anti-PR3, and anti-GBM respectively. In eosinophilic granulomatosis with polyangiitis (EGPA) 87.5% (7/8), and microscopic polyangiitis (MPA/RLV) 91.3% (21/23), anti-MPO was the predominantly observed antibody. In granulomatosis with polyangiitis (GPA) anti-PR3 antibody was predominant in 87.5% (28/32) cases. Out of 168 IIF positive samples 8, 32, and 23 cases of EGPA, GPA, and MPA/RLV were observed respectively.

CONCLUSIONS:

The primary aim of the study was to provide single-centre data to determine the laboratory diagnosis of AAV. A combination of IIFT and LIA was found to be an optimum testing strategy for the laboratory diagnosis of AAV.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Churg-Strauss / Granulomatose com Poliangiite / Vasculite Associada a Anticorpo Anticitoplasma de Neutrófilos Tipo de estudo: Diagnostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Churg-Strauss / Granulomatose com Poliangiite / Vasculite Associada a Anticorpo Anticitoplasma de Neutrófilos Tipo de estudo: Diagnostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article