Since several forms of autoimmunity have been associated with urticaria, we
performed a detailed survey of autoantibodies in patients with idiopathic
subacute and chronic urticaria. Sera from 25 consecutive patients referred
for evaluation of urticaria were. tested for the presence of autoantibodies
and compared to sera from seventy-five control samples examined from indiv
iduals being treated for other allergic diseases. Study patients ranged in
age from 15 to 73 years, with a mean of 48. One patient had a diagnosis of
inflammatory bowel disease and one had multiple myeloma, but otherwise ther
e were no other diagnoses of disease specifically involving immunity other
than atopy. No study patients had a concurrent diagnosis of autoimmune thyr
oid disease. The test sera were examined for autoantibodies and for antibod
ies to H. pylori. Antibodies to thyroid peroxidase (TPO) were found signifi
cantly (p < 0.01) more common in urticaria (20%] than in controls (0%). Rhe
umatoid factor(RF) was also found in significantly (p < 0.05) increased in
urticaria (16%) compared to controls [0%). Neither H. pylori antibody nor o
ther autoantibodies were present in significant numbers of urticaria patien
ts when compared to controls. Tested autoantibodies included those to thyio
globulin, sDNA, SSA/SSB, ENA, cardiolipin, beta2-glycoprotein I, myeloperox
idase, proteinase-3, smooth muscle, ANA, human lysosamal-associated membran
e protein, and bactericidal permeability increasing protein. Thus, patients
with:urticaria were somewhat more likely to have a thyroid autoantibody to
TPO or to have RF. This survey demonstrates that while some markers of aut
oimmunity may be increased in urticaria patients, broad nonspecific autoimm
unity is not found.