Halperin W, Weiss W I, Altman R, Diamond M A, Black K J, Iaci A W, Black H C, Goldfield M
Am J Public Health. 1979 Dec;69(12):1247-51. doi: 10.2105/ajph.69.12.1247.
A trail of influenza vaccination, with use of bivalent split virus vaccine (A/New Jersey/76 and A/Victoria/75), was conducted to compare the immunogenicity and reactions when vaccine was given by the subcutaneous and intradermal routes. Volunteers 18 to 24 years old were randomized into equal groups, one group receiving 0.1 ml of vaccine intradermally and the other receiving 0.5 ml subcutaneously. For the A/Victoria vaccine, the immunogenicity of the intradermal route seemed superior; for A/New Jersey vaccine, the routes were equivalent. Adverse reactions were minimal and equivalent for both groups. In times of vaccine shortage, the intradermal route is considered to stretch vaccine supplies. Field trials of new influenza vaccines should include evaluation of the immunogenicity of and adverse reactions caused by the same vaccine given by different routes in varied dosages.
开展了一项流感疫苗接种试验,使用二价裂解病毒疫苗(A/新泽西/76和A/维多利亚/75),以比较皮下注射和皮内注射疫苗时的免疫原性和反应。18至24岁的志愿者被随机分为相等的两组,一组接受0.1毫升皮内注射疫苗,另一组接受0.5毫升皮下注射疫苗。对于A/维多利亚疫苗,皮内注射途径的免疫原性似乎更好;对于A/新泽西疫苗,两种途径相当。两组的不良反应均轻微且相当。在疫苗短缺时期,皮内注射途径被认为可以延长疫苗供应。新型流感疫苗的现场试验应包括评估不同剂量的同一疫苗通过不同途径接种时的免疫原性和不良反应。