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Binding of specific IgE antibodies from the sera of patients allergic to animals was investigated by direct RAST, using the animal's dander, urine, saliva or blood serum as insolubilized allergens. In allergy to rat, mouse, guinea pig, dog, cat or horse, the RAST results with the excretions of a particular animal were mutually well correlated. RAST with the animal blood serum was positive less often, and only in cases of a positive dander RAST. It is concluded that a RAST with animal dander precludes the use of other animal products.

The distribution of the major allergen of the domestic cat, cat allergen 1, was studied in 22 different tissues obtained from a male and female cat and in samples of saliva and urine. Of the cat tissues studied, only extracts of pelt and female brain contained amounts of cat allergen 1 in excess of 0.50 U/ml. Smaller amounts of cat allergen 1 were found in extracts of eye, thyroid, ovary, sublingual gland and large intestine. Unstimulated cat saliva contained a mean of 1.08 U/ml cat allergen 1. Saliva stimulated with ketamine HCl alone, or with ketamine HCl plus pilocarpine, contained 0.68-8.16 U/ml cat allergen 1. In all of the stimulated saliva collections, the total quantity of cat allergen 1 obtained was relatively constant (between 40 and 80 U). These results suggested that the elaboration of cat allergen 1 in saliva is independent of parasympathetic control. Cat allergen 1 could only be detected in cat urine that had been concentrated 9-fold in concentrations of less than 0.5 U/ml. The above results support the hypothesis that the major source of cat allergen 1 is the saliva, and that the presence of cat allergen 1 in the pelt is due to deposition of the allergen during grooming.

A survey of hepatitis B patients, asymptomatic hepatitis B antigen (HBsAg) carriers, and control subjects was conducted to determine the relationship between antigenemia and antigen excretion in saliva, urine, and stool. Radioimmunoassay was used to detect HBsAg. Specificity-confirmed HBsAg was detected in the saliva of 6 (30%) of 20 antigenemic patients, 1 (5%) of 20 nonantigenemic patients, 14 (34%) of 41 carriers, and 0 of 112 controls. HBsAg was detected in urine only after 100-fold concentration of first-morning specimens. Specificity-confirmed HBsAg was present in the urine of 7 (16%) of 43 carriers; unconfirmed HBsAg was found in the urine of 5 (13%) of 38 patients and 5 (5%) of 112 controls. Unconfirmed HBsAg was detected in concentrated stool specimens from 5 (46%) of 11 patients and 3 of 8 carriers and controls. Longitudinally collected specimens from antigenemic subjects showed no consistent patterns of antigen excretion.