LabMedica

Download Mobile App
Recent News Expo Clinical Chem. Molecular Diagnostics Hematology Immunology Microbiology Pathology Technology Industry Focus

Anti-Double Stranded DNA Antibodies Diagnose Systemic Lupus Erythematosus

By LabMedica International staff writers
Posted on 13 Jul 2022
Print article
Image: Kallestad Anti-dsDNA EIA, Bio-Rad Autoimmune Anti-dsDNA EIA and Bio-Rad Autoimmune EIA Anti-ssDNA. Anti-DNA testing is intended for use in the diagnosis and management of systemic lupus erythematosus (SLE) and certain other rheumatic diseases (Photo courtesy of Bio-Rad)
Image: Kallestad Anti-dsDNA EIA, Bio-Rad Autoimmune Anti-dsDNA EIA and Bio-Rad Autoimmune EIA Anti-ssDNA. Anti-DNA testing is intended for use in the diagnosis and management of systemic lupus erythematosus (SLE) and certain other rheumatic diseases (Photo courtesy of Bio-Rad)

Anti-double-stranded deoxyribonucleic acid antibodies (anti-dsDNA Abs) embrace antibodies with a wide spectrum of fine molecular specificities that are produced persistently in the context of true autoimmunity or transiently in context of infections or other clinical conditions.

Numerous studies have yielded insight into specific aspects of anti-dsDNA Abs, such as their genetics, immunogens and targets, as well as their diagnostic and pathogenic impact, particularly in Systemic Lupus Erythematosus (SLE). The clinical significance of anti-dsDNA Abs largely depends on the principle of the assay employed and the analytical variables of the methods used to quantify and characterize them.

A team of Immunologists at the University Hospital Mohamed VI (Marrakech, Morocco) and their colleagues carried out a cross-sectional study on 113 adults and pediatric patients presenting various clinical conditions that included 53 SLE, other systemic autoimmune rheumatic diseases (OSARD) including 23 rheumatoid arthritis, nine Sjögren syndrome, eight mixed connective tissue disease (MCTD) five systemic sclerosis (SSc, inflammatory myositis (IM), and 10 non-auto-immune clinical conditions (NAICC), including five patients with inflammatory neurologic diseases and five cases of non-lupus glomerulonephritis. The mean age of patients was 39.9 ± 15 years (range, 11–85 years), and they were predominantly females (female to male sex ratio = 4.94).

Blood samples collected from the patients and serum samples were tested for anti-dsDNA Abs using the ELISA Kallestad Anti-dsDNA EIA, IgG conjugate (Bio-Rad Laboratories, Hercules, CA, USA) combined with and Crithidia luciliae fluorescence test (CLIFT, Kallestad, Bio-Rad), threshold: 1:10). Screening for ANA was performed by the IIF method using a Hep-2 cell substrate (Kallestad, Bio-Rad), threshold: 1:160 for patients older than 18 and 1:80 for those younger than 18).

The investigators reported that overall, 42.4% (n = 48), 27.4% (n = 31), and 78.8% (n = 89) of patients with selected clinical conditions were positive for DNA-ELISA, DNA-CLIFT, and ANA-IIFA anti-dsDNA Ab screening, respectively The proportion of ELISA-positive patients with SLE was more than that of CLIFT-positive ones (77.3% versus 54.7%). The DNA-ELISA test was positive for 48 patients (42.4%), among whom 34 patients had titers higher than 50 IU/mL, 16 patients had titers varying between 30 and 50 IU/mL, whereas 32 patients had equivocal titers (15–30 IU/mL), and 31 patients were negative. ANA were positive for 78.7% of patients, including 48 patients (90.5%) with SLE. Among the 50 patients positive for DNA-ELISA, 31 (62%) were also positive for CLIFT, and these patient were significantly associated with high titers of DNA-ELISA.

The authors concluded that a diagnostic strategy based on the detection and quantification of anti-dsDNA Abs by ELISA, followed if positive by CLIFT and ANA-IIF screening. High titers of anti-DNA Abs on ELISA associated with positive CLIFT are almost relevant, especially when associated with a homogeneous ANA-IIF pattern, taking into consideration the clinical criteria of SLE. The study was published on June 9, 2022 in the journal Practical Laboratory Medicine.

Related Links:
University Hospital Mohamed VI 
Bio-Rad Laboratories 

Gold Member
Pharmacogenetics Panel
VeriDose Core Panel v2.0
Verification Panels for Assay Development & QC
Seroconversion Panels
New
Toxoplasma Gondii Immunoassay
Toxo IgM AccuBind ELISA Kit
New
Community-Acquired Pneumonia Test
RIDA UNITY CAP Bac

Print article

Channels

Molecular Diagnostics

view channel
Image: The study investigated D-dimer testing in patients who are at higher risk of pulmonary embolism (Photo courtesy of Adobe Stock)

D-Dimer Testing Can Identify Patients at Higher Risk of Pulmonary Embolism

Pulmonary embolism (PE) is a commonly suspected condition in emergency departments (EDs) and can be life-threatening if not diagnosed correctly. Achieving an accurate diagnosis is vital for providing effective... Read more

Immunology

view channel
Image: The findings were based on patients from the ADAURA clinical trial of the targeted therapy osimertinib for patients with NSCLC with EGFR-activated mutations (Photo courtesy of YSM Multimedia Team)

Post-Treatment Blood Test Could Inform Future Cancer Therapy Decisions

In the ongoing advancement of personalized medicine, a new study has provided evidence supporting the use of a tool that detects cancer-derived molecules in the blood of lung cancer patients years after... Read more

Microbiology

view channel
Image: Schematic representation illustrating the key findings of the study (Photo courtesy of UNIST)

Breakthrough Diagnostic Technology Identifies Bacterial Infections with Almost 100% Accuracy within Three Hours

Rapid and precise identification of pathogenic microbes in patient samples is essential for the effective treatment of acute infectious diseases, such as sepsis. The fluorescence in situ hybridization... Read more
Sekisui Diagnostics UK Ltd.