Antibodies to DNA, either single or double-stranded, are
found primarily in systemic lupus erythematosus, and are
important, but not necessary or sufficient for diagnosing
that condition. Such antibodies are present in 80% to 90%
of SLE cases. They are also present in smaller fractions of
patients with other rheumatic disorders, and in chronic
active hepatitis, infectious mononucleosis, and biliary
cirrhosis. In the past it was considered unnecessary to
test for anti-DNA in patients with a negative test for
antinuclear antibodies. A group of "ANA negative lupus"
patients has been described with anti-ssDNA and anti-SS-
A/Ro and anti-SS-B/La. However, HEp-2 substrate is much
more sensitive than frozen section substrates, and it is
uncommon for anti-SS-A/Ro to be negative with these newer
substrates.
This standard dsDNA detects both low- and
high-affinity antibodies, providing a very sensitive test
for diagnostic purposes; however, it is less predictive for
severe nephritis, which is associated with the presence of
high-affinity antibodies.
Following levels of anti-DNA
antibody may be of use in evaluating response to therapy,
but should be regarded as a guide rather than a rigid
dictator of treatment. Antibody levels correlate
particularly well with activity of lupus nephritis.
Procainamide and hydralazine may induce anti-DNA
antibodies, and antihistone antibodies.