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A Comparative Trial of Oil-Adjuvant and Aqueous Polyvalent Influenza Vaccines

机译:油佐剂和水性多价流感疫苗的比较试验

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摘要

In the early autumn of 1963, 957 volunteers were inoculated with Admune (an oil-adjuvant polyvalent influenza vaccine) and 337 with Munevan (an aqueous polyvalent vaccine).A survey by questionnaire suggested that the oil-adjuvant vaccine was more acceptable to the inoculated than the aqueous one. The oil-adjuvant vaccine seemed less likely than the aqueous to provoke serious side effects in unknown reactors, and this more than offset the possibility of subcutaneous nodules not encountered with the aqueous vaccine. No difficulty was encountered in administering the oil-adjuvant vaccine, in the recommended dose, to those giving a history of hay fever, asthma, and some other major allergies.On this occasion, reactions to both vaccines were fairly prevalent, and about a quarter of all those vaccinated complained of a feeling of malaise lasting at least two weeks. These reactions were thought to be severe enough to induce consumer-resistance to routine annual immunization, which is considered hardly acceptable in a healthy industrial population at the present stage of development. Medically the case for such immunization is not yet proven.There is a need for further vaccine development and for more controlled trials. If the efficacy of the oil-adjuvant vaccine is proved in clinical practice, this vaccine appears preferable to the aqueous type.
机译:在1963秋初,有957名志愿者接种了Admune(一种油佐剂多价流感疫苗),而337名接种了Munevan(一种水剂多价流感疫苗),通过问卷调查表明,油佐剂疫苗更容易被接种比水性的油佐剂疫苗似乎不像水佐剂疫苗在未知的反应堆中引起严重的副作用,这远远抵消了水佐剂未遇到皮下结节的可能性。在有花粉症,哮喘和其他一些严重过敏史的人中,建议剂量的油佐剂疫苗接种没有遇到困难。在这种情况下,两种疫苗的反应相当普遍,大约四分之一所有接受过疫苗接种的人抱怨至少持续了两周的不适感。这些反应被认为严重到足以引起消费者对常规年度免疫的抵抗力,在目前的发展阶段,这被认为对于健康的工业人群来说是难以接受的。在医学上,这种免疫的情况尚未得到证实。需要进一步的疫苗开发和更受控的试验。如果在临床实践中证明了油佐剂疫苗的功效,那么这种疫苗似乎比水性疫苗更可取。

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