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Factors affecting IgA related hyperviscosity.

U Alkner, U B Hansson, F D Lindström

    Clinical and Experimental Immunology
    |March 1, 1983
    PubMed
    Summary
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    High IgA concentrations in patients with IgA M-component can cause hyperviscosity. This study investigated the molecular properties of IgA contributing to hyperviscosity in monoclonal gammopathy.

    Area of Science:

    • Immunology
    • Biochemistry
    • Hematology

    Background:

    • Immunoglobulin A (IgA) M-component is associated with various hematological conditions.
    • Hyperviscosity syndrome (HVS) can complicate monoclonal gammopathies, impacting patient health.
    • Understanding the molecular basis of IgA hyperviscosity is crucial for diagnosis and management.

    Purpose of the Study:

    • To investigate the physicochemical properties of IgA M-components in patients with monoclonal gammopathy.
    • To determine the relationship between IgA concentration, molecular form (monomeric/dimeric), and hyperviscosity.
    • To explore the role of hydrophobic interactions and microenvironmental factors in IgA-induced hyperviscosity.

    Main Methods:

    • Analysis of serum samples from 14 patients with IgA M-component (6 myelomatosis, 8 benign monoclonal gammopathy).

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  • Measurement of serum IgA and total protein concentrations.
  • Assessment of hyperviscosity (HV) and hyperviscosity syndrome (HVS).
  • Circular dichroism and hydrophobic interaction chromatography to analyze IgA structure and properties.
  • Main Results:

    • All six patients with high IgA (>40 g/l) and total protein (>100 g/l) concentrations exhibited hyperviscosity.
    • Four of these patients presented with hyperviscosity syndrome.
    • No correlation was found between IgA dimers/polymers and the presence of HV or HVS.
    • Differences in the microenvironment and hydrophobicity of monomeric and dimeric IgA were observed between normal and myeloma sera.

    Conclusions:

    • Elevated IgA and total protein levels are strongly associated with hyperviscosity in IgA M-component disorders.
    • The quantity of IgA dimers or polymers does not directly correlate with hyperviscosity.
    • Hydrophobic interactions and alterations in the IgA microenvironment may play a significant role in the development of hyperviscosity.