Newman Peter A, Duan Naihua, Lee Sung-Jae, Rudy Ellen T, Seiden Danielle S, Kakinami Lisa, Cunningham William E
Centre for Applied Social Research, University of Toronto, Faculty of Social Work, 246 Bloor Street West, Toronto, Ont., Canada M5S 1A1.
Vaccine. 2006 Mar 15;24(12):2094-101. doi: 10.1016/j.vaccine.2005.11.013. Epub 2005 Nov 21.
HIV vaccines offer the best long-term hope of controlling the AIDS pandemic; yet, the advent of HIV vaccines will not ensure their acceptability. We conducted a cross-sectional survey (n=143), incorporating conjoint analysis, to assess HIV vaccine acceptability among participants recruited using multi-site (n=9), venue-based sampling in Los Angeles. We used a fractional factorial experimental design to construct eight hypothetical HIV vaccines, each with seven dichotomous attributes. The acceptability of each vaccine was assessed individually and then averaged across participants. Next, the impact of each attribute on vaccine acceptability was estimated for each participant using ANOVA and then analyzed across participants. Acceptability of the eight hypothetical HIV vaccines ranged from 33.2 (S.D. 34.9) to 82.2 (S.D. 31.3) on a 0-100 scale; mean=60.0 (S.D. 21.9). Efficacy had the greatest impact on acceptability (22.7; CI: 18.5-27.1; p<0.0001), followed by cross-clade protection (12.5; CI: 8.7-16.3, p<0.0001), side effects (11.5; CI: 7.4-15.5; p<0.0001), and duration of protection (6.1; CI: 3.2-9.0; p<.0001). Route of administration, number of doses and cost were not significant. Low acceptability of "partial efficacy" vaccines may present obstacles to future HIV vaccine dissemination. Educational and social marketing interventions may be necessary to ensure broad HIV vaccine uptake.
艾滋病毒疫苗为控制艾滋病大流行带来了最有希望的长期解决方案;然而,艾滋病毒疫苗的出现并不能确保其被接受。我们进行了一项横断面调查(n = 143),采用联合分析,以评估在洛杉矶通过多地点(n = 9)、基于场所的抽样招募的参与者对艾滋病毒疫苗的接受程度。我们使用分数因子实验设计构建了八种假设的艾滋病毒疫苗,每种疫苗具有七个二分属性。分别评估每种疫苗的可接受性,然后在参与者中求平均值。接下来,使用方差分析为每个参与者估计每个属性对疫苗可接受性的影响,然后在参与者中进行分析。在0 - 100的量表上,八种假设的艾滋病毒疫苗的可接受性范围为33.2(标准差34.9)至82.2(标准差31.3);平均值 = 60.0(标准差21.9)。疗效对可接受性的影响最大(22.7;置信区间:18.5 - 27.1;p < 0.0001),其次是跨亚型保护(12.5;置信区间:8.7 - 16.3,p < 0.0001)、副作用(11.5;置信区间:7.4 - 15.5;p < 0.0001)和保护持续时间(6.1;置信区间:3.2 - 9.0;p <.0001)。给药途径、剂量数量和成本不显著。“部分疗效”疫苗的低接受度可能会给未来艾滋病毒疫苗的推广带来障碍。可能需要开展教育和社会营销干预措施,以确保广泛接受艾滋病毒疫苗。