Resolution of Spurious Immunonephelometric IgG Subclass Measurement Discrepancies by LC-MS/MS

Author:

van der Gugten Grace1,DeMarco Mari L12,Chen Luke Y C23,Chin Alex45,Carruthers Mollie26,Holmes Daniel T12,Mattman Andre12

Affiliation:

1. Department of Pathology and Laboratory Medicine, St. Paul's Hospital, Vancouver, BC, Canada

2. Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada

3. Division of Hematology, Vancouver General Hospital, Vancouver, BC, Canada

4. Department of Pathology and Laboratory Medicine, Calgary Laboratory Services, Calgary, AB, Canada

5. Cumming School of Medicine, University of Calgary, Calgary, AB, Canada

6. Division of Rheumatology, Vancouver General Hospital, Vancouver, BC, Canada

Abstract

Abstract BACKGROUND The Binding Site immunonephelometric (IN) IgG subclass reagents (IgG1, IgG2, IgG3, IgG, BSIN) are used for assessment of both immunodeficiency and IgG4-related disease (IgG4-RD). In our laboratory, suspected analytic errors were noted in patients with increases in IgG4: The sum of the individual IgG subclasses was substantially greater than the measured total IgG concentrations (unlike samples with normal IgG4), and the IgG4 concentration was always less than the IgG2 concentration. METHODS We developed a tryptic digest LC-MS/MS method to quantify IgG1, IgG2, IgG3, and IgG4 in serum. Samples with IgG4 concentrations ranging from <0.03 g/L to 32 g/L were reanalyzed by LC-MS/MS, and a subset was also reanalyzed by Siemens IN (SIN) subclass measurements. RESULTS Multivariate linear regression identified 3 subclass tests with multiple predictors of the measured subclass concentration. For these 3 subclasses, the predominant predictors were (in terms of LC-MS/MS IgG subclass measurement coefficients) BSIN IgG1 = 0.89·IgG1 + 0.4·IgG4; BSIN IgG2 = 0.94·IgG4 + 0.89·IgG2; and SIN IgG2 = 0.72·IgG2 + 0.24·IgG4. CONCLUSIONS There is apparent IgG4 cross-reactivity with select IN subclass measurements affecting tests from both vendors tested. These findings can be explained either by direct cross-reactivity of the IN reagents with the IgG4 subclass or unique physicochemical properties of IgG4 that permit nonspecific binding of IgG4 heavy chain to other IgG immunoglobulin heavy chains. Irrespective of the mechanism, the observed intermethod discrepancies support the use of LC-MS/MS as the preferred method for measurement of IgG subclasses when testing patients with suspected IgG4-RD.

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

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