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Immune complexes in progressive systemic sclerosis and mixed connective tissue disease
The Journal of Rheumatology
|May 1, 1980
Summary
This study found circulating immune complexes (CICs) in most patients with mixed connective tissue disease (MCTD) and progressive systemic sclerosis (PSS). The Raji cell assay was most sensitive, with higher CIC levels correlating with disease activity in MCTD.
Area of Science:
- Immunology
- Rheumatology
- Clinical Chemistry
Background:
- Circulating immune complexes (CICs) are implicated in autoimmune diseases.
- Progressive systemic sclerosis (PSS) and mixed connective tissue disease (MCTD) are systemic autoimmune disorders.
Purpose of the Study:
- To investigate the presence and levels of CICs in patients with PSS and MCTD.
- To compare the sensitivity of different assays for CIC detection.
- To explore the relationship between CIC levels and disease activity.
Main Methods:
- Sera from PSS and MCTD patients were analyzed for CICs using Clq precipitins, cryoglobulins, and radioimmunoassays (Raji cell and Clq).
- The Raji cell assay was identified as the most sensitive method for CIC detection.
Main Results:
- The Raji cell assay detected CICs in 82% of MCTD patients and 55% of PSS patients.
- Median CIC levels were significantly higher in MCTD (79 µg eq AHG/ml) compared to PSS (20 µg eq AHG/ml).
- In MCTD, CIC levels correlated with disease activity, unlike in PSS.
Conclusions:
- The Raji cell assay is a sensitive tool for detecting CICs in PSS and MCTD.
- Elevated CIC levels, particularly those correlating with disease activity, may be more characteristic of MCTD than PSS.
- Ribonucleoprotein (RNP) antigen was not found in the detected immune complexes.