High frequency of concurrent anti-C1q and anti-dsDNA but not anti-C3b antibodies in patients with Lupus Nephritis.


Journal

Journal of immunoassay & immunochemistry
ISSN: 1532-4230
Titre abrégé: J Immunoassay Immunochem
Pays: England
ID NLM: 100963688

Informations de publication

Date de publication:
04 Jul 2021
Historique:
pubmed: 1 4 2021
medline: 1 9 2021
entrez: 31 3 2021
Statut: ppublish

Résumé

Lupus Nephritis (LN) in patients with Systemic Lupus Erythematosus (SLE) is one of the most serious and prevalent manifestations. The procedure of renal biopsy is harmful and accompanied by potential hazards. Therefore, introducing reliable biomarkers to predict LN is exceedingly worthwhile. In the present study, we compared the diagnostic values of circulating autoantibodies against dsDNA, C1q, C3b, SSA, SSB, and Sm alone or in combination to predict LN. This study evaluated the abovementioned autoantibodies in 40 healthy controls (HCs) and 95 SLE patients with different kidney involvements, including absent (n = 40), inactive (n = 20), and active (n = 35) LN using EIA method. The frequency and odds ratio of anti-dsDNA (71.4%, OR = 4.2), anti-C1q (62.9%, OR = 5.1), and the simultaneous existence of anti-C1q and anti-dsDNA (51.4%, OR = 6) antibodies were significantly higher in the active LN group compared with both inactive and absent LN groups. Moreover, the levels of anti-C1q and anti-dsDNA antibodies positively correlated with disease activity in patients with SLE. The prevalence of these autoantibodies was associated with the severity of LN biopsies. These data suggest that anti-C1q and anti-dsDNA antibodies and also their simultaneous presence may be valuable diagnostic biomarkers for LN prediction in patients with SLE.

Identifiants

pubmed: 33788670
doi: 10.1080/15321819.2021.1895215
doi:

Substances chimiques

Autoantibodies 0
Complement C1q 80295-33-6
DNA 9007-49-2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

406-423

Auteurs

Nahid Kianmehr (N)

Department of Rheumatology, Iran University of Medical Sciences, Tehran, Iran.

Majid Khoshmirsafa (M)

Department of Immunology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Immunology Research Center, Institute of Immunology and Infectious Diseases Iran University of Medical Sciences, Tehran, Iran.

Mehdi Shekarabi (M)

Department of Immunology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Immunology Research Center, Institute of Immunology and Infectious Diseases Iran University of Medical Sciences, Tehran, Iran.

Reza Falak (R)

Department of Immunology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Immunology Research Center, Institute of Immunology and Infectious Diseases Iran University of Medical Sciences, Tehran, Iran.

Anousheh Haghighi (A)

Department of Rheumatology, Iran University of Medical Sciences, Tehran, Iran.

Mohammad Masoodian (M)

Department of Immunology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.

Farhad Seif (F)

Academic Center for Education, Culture and Research, Tehran, Iran.

Forouzan Omidi (F)

Department of Immunology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.

Fatemeh Shirani (F)

Department of Rheumatology, Iran University of Medical Sciences, Tehran, Iran.

Nima Dadfar (N)

Department of Rheumatology, Iran University of Medical Sciences, Tehran, Iran.

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Classifications MeSH