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首页> 外文期刊>Vaccine >Comparison of the safety, tolerability, and immunogenicity of a MF59-adjuvanted influenza vaccine and a non-adjuvanted influenza vaccine in non-elderly adults
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Comparison of the safety, tolerability, and immunogenicity of a MF59-adjuvanted influenza vaccine and a non-adjuvanted influenza vaccine in non-elderly adults

机译:非老年人中MF59辅助流感疫苗和非辅助流感疫苗的安全性,耐受性和免疫原性的比较

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摘要

The adjuvanted influenza vaccine FLUAD(TM) is composed of subunit influenza antigens combined with the MF59-adjuvant emulsion. The vaccine was developed primarily for use in elderly populations, but non-elderly individuals might also benefit. To evaluate this hypothesis, 301 healthy adults were assigned randomly to receive two intramuscular injections of either FLUAD(TM) (150 subjects) or a non-adjuvanted vaccine, Fluzone(TM) (151 subjects), in two trials conducted at a 1-year interval. Injections consisted of 15 mug per 0.5 ml dose. Vaccine composition was A/Texas/36/91 (H1N1), A/Johannesburg/33/94 (H3N2), and B/Harbin/7/94 for the first injection and A/Texas/36/91 (H1N1), A/Nanchang/933/95 (H3N2), and B/Harbin/7/94 for the second injection. Immunogenicity was evaluated at 28 and 180 days post-immunization. FLUAD(TM) was generally well tolerated in healthy adults when compared with Fluzone(TM). FLUAD(TM) was associated with increased pain at the injection site after immunization. A statistically significant increase in the incidence of injection-site warmth, chills, myalgia, and analgesic/antipyretic use occurred in the FLUAD(TM) group after the first injection but not after the second injection. In both groups, most of these local and systemic reactions were classified as mild. FLUAD(TM) was more immunogenic than Fluzone TM following both injections. After the first injection, statistically significant differences were found in the percentage of subjects with four-fold rises in hemagglutinin inhibition (III) titers at 28 days post-immunization for the B antigen. After the second injection, the FLUADTM group had significantly higher HI titers, a significantly higher percentage with a four-fold increase in titer, and a significantly greater percentage of subjects with titers greater than or equal to 160 for the H3N2 antigen at 28 days. Only minor immunogenicity differences between the two groups were seen at 180 days. Compared with Fluzone(TM), FLUAD(TM) was associated with increased immunogenicity and mild post-immunization reactions in healthy adults. The magnitude of increased immunogenicity in healthy adults was less than that seen in elderly populations.
机译:佐剂型流感疫苗FLUAD TM由亚单位流感抗原与MF59-佐剂乳剂结合组成。该疫苗主要用于老年人群,但非老年人也可能会受益。为了评估该假设,在1项试验中,以1项进行了两项试验,随机分配了301名健康成年人接受两次FLUAD™(150名受试者)或非佐剂疫苗Fluzone™(151名受试者)的肌肉注射。年间隔。注射量为每0.5 ml剂量15杯。第一次注射的疫苗成分为A / Texas / 36/91(H1N1),A / Johannesburg / 33/94(H3N2)和B / Harbin / 7/94,以及首次注射的A / Texas / 36/91(H1N1),A / Nanchang / 933/95(H3N2)和B / Harbin / 7/94进行第二次注射。在免疫后28和180天评估免疫原性。与FluzoneTM相比,健康成年人通常对FLUAD™的耐受性良好。免疫后,FLUAD TM与注射部位疼痛增加有关。在第一次注射后但在第二次注射后没有发生FLUAD TM组中注射部位的发热,寒战,肌痛和止痛/解热的使用发生率的统计上显着增加。在两组中,大多数这些局部和全身反应被分类为轻度。两次注射后,FLUAD TM均比Fluzone TM更具免疫原性。首次注射后,在B抗原免疫后28天血凝素抑制(III)滴度上升四倍的受试者百分比中发现统计学上的显着差异。第二次注射后,FLUADTM组的HI效价显着更高,在28天时H3N2抗原的效价大于或等于160的受试者显着更高的百分比,其效价增加了四倍。在180天时,两组之间只有很小的免疫原性差异。与Fluzone™相比,FLUAD™与健康成人的免疫原性增加和轻度的免疫后反应相关。健康成年人的免疫原性增加的幅度小于老年人群。

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