It was lately disclosed that mumps is not a localized disease of the parotid gland, but a generalized infection, caused by mumps virus. In recent years, it was revealed furthermore, that a certain type of aseptic lymphocytic meningoencephalitis is comprised in the group of mumps infection. The prevention of the disease has thus become a matter of importance in pediatrics. In order to establish reasonable preventive measures against mumps, it is necessary to make clear the epidemiologic characteristics of this infection. Indispensable to the investigation is a reliable skin test, which enables the investigator to make an accurate estimation of the grade of group sensitivity or of the immunity of community inhabitants to this disease.
The first report on the skin test of mumps was that of Enders, which was followed by the reports of Cabasso, Henle, Kono, Ashiwara and other investigators. The antigens employed by them, however, were not of uniform property, and they were evaluated with various methods, which made an application of these antigens to epidemiologic investigations impossible. In the present report, the author made an attempt to devise an adequate standardization method with an antigen of constant potency.
According to a comparative study of Ashiwara, the antigen solutions which were employed by the above-mentioned investigators, all contained the antigen of complement fixation test in a concentration of 1 u/0.2 ml approximately. Among these antigens, Henle's so-called soluble antigen was characterized by its constant potency and by the least stimulation to antibody production. For these reasons, Henle's antigen and a corresponding control solution were employed in the present investigation.
0.1 mg of the antigen and the control solution were carefully injected intracutaneously on the inner side of forearms of 431 examinees, who had been divided into 3 groups of 80, 208 and 143, to each of which one of 3 lots of the antigen was given. The diameter of the resulting erythema was measured in 24 and 48 hours, and its frequency distribution was pursued statistically.
Statistical analysis justified the following standard f or the estimation of the skin reaction.
The reaction must be evaluated by the size of erythemae 48 hours after the injection. Erythemae larger than 10 mm in diameter represent a positive reaction. Those smaller than 4 mm in diameter a negative. In the range from 5 to 9 mm the reaction is an ambiguous one.
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