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Chinese Journal of Clinicians(Electronic Edition) ›› 2019, Vol. 13 ›› Issue (10): 736-739. doi: 10.3877/cma.j.issn.1674-0785.2019.10.004

Special Issue:

• Clinical Research • Previous Articles     Next Articles

Diagnostic value of antinuclear antibody spectrum detected with a fully automated BioPlexTM 2200 immunoassay analyzer in patients with systemic lupus erythematosus

Xinlan Pan1, Zhijun Li1,(), Chao Jiang1, Ying Zhou1, Mengjie Liu2, Jiao Liu1   

  1. 1. Department of Rheumatology, the First Affiliated Hospital of Bengbu Medical College, Bengbu 233000, China
    2. Department of Rheumatology, the Second Affiliated Hospital of Bengbu Medical College, Bengbu 233000, China
  • Received:2019-03-23 Online:2019-05-15 Published:2019-05-15
  • Contact: Zhijun Li
  • About author:
    Corresponding author: Li Zhijun, Email:

Abstract:

Objective

To evaluate the value of antinuclear antibody (ANA) spectrum detected with a fully automated BioPlex 2200 immunoassay analyzer in the diagnosis of systemic lupus erythematosus (SLE).

Methods

We used a fully automated BioPlexTM 2200 immunoassay analyzer and enzyme-linked immunosorbent assay (ELISA) method to detect dsDNA, Sm, and RNP antibodies in 30 cases of systemic lupus erythematosus. Fifteen ANAs were then detected with the fully automated BioPlexTM 2200 immunoassay analyzer in 251 serum samples (including 109 from patients with SLE, 109 from patients with connective tissue disease, and 33 from healthy controls) and statistically analyzed. Other laboratory indexes were tested using routine methods.

Results

The positive rates of anti-dsDNA, anti-nuclear chromatin, anti-po, Sm, SmRNP, RNP, RNP68, SSA, RNP-A, Ro60, Ro52, and SSB had significant differences between the connective tissue disease group and healthy control group (P<0.05). The positive rate of CenB in the SLE group was comparable to those of the connective tissue disease group and healthy control group (P>0.05). There was a significant difference in the positive rate of any ANAs between the SLE group and the control group (P<0.05), but there was no significant difference between the connective tissue group and healthy control group (P>0.05). The two methods had a good consistency in the detection of dsDNA, Ro60, SSB, and Po (Kappa=0.79, 0.87, 0.76, and 0.80, respectively), and a fair consistency in the detection of Sm, RNP, and Ro52 (Kappa=0.61, 0.60, and 0.50, respectively).

Conclusion

Detection of antinuclear antibody spectrum with a fully automated BioPlexTM 2200 immunoassay analyzer has appreciated clinical value in the diagnosis of SLE. The ability of flow matrix immunoluminescence assay to detect antinuclear antibody spectrum is comparable to that of ELISA.

Key words: Lupus erythematosus, systemic, Antibodies, antinuclear, Fully automated BioPlex 2200 immunoassay analyzer

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