The
quantitative assay of hemolytic complement activity depends on the ability
of the primary complement pathway to induce hemolysis of red cells sensitized
with optimal amounts of anti-red cell antibodies. For precise titrations
of hemolytic complement, the dilution of serum that will lyse 50% of the
indicator red cells is determined as the CH50. This arbitrary unit depends
on the conditions of the assay and is therefore laboratory-specific.
Normal Range: Laboratory-specific U/mL
Decreased
with: >50-80% deficiency of primary pathway complement components in congenital
or acquired deficiency.
Normal in: Deficiencies
of alternative pathway, complement components.
Additional: This
is a functional assay of biologic activity. Sensitivity to decreased levels
of complement components depends on exactly how the test is performed.
It is used to detect congenital and acquired severe deficiency disorders
of the primary complement pathway.
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