FIELD: medicine, dermatovenerology. SUBSTANCE: method involves the preliminary assay of antibodies in blood to cytoplasmatic antigen and at value below 2.84 ± 0.21 ln1/titer the native staphyloprotectin is administrated subcutaneously at dose 0.2-0.3-0.5-0.8 ml at 3 days interval and then after 2 months adsorbed staphyloprotectin is administrated as a single dose 0.8 ml. EFFECT: improved method of treatment. 3 tbl
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Authors
Dates
1996-08-27—Published
1993-02-26—Filed