Meningitis and Vaccine Preventable Diseases Branch, Division of Bacterial Diseases, National Center for Immunization and Respiratory Diseases, US Centers for Disease Control and Prevention, Atlanta, Georgia.
JAMA Pediatr. 2016 May 1;170(5):453-8. doi: 10.1001/jamapediatrics.2015.4875.
There is accumulating literature on waning acellular pertussis vaccine-induced immunity, confirming the results of studies assessing the duration of protection of pertussis vaccines.
To evaluate the tetanus toxoid, reduced diphtheria toxoid, and acellular pertussis (Tdap) vaccine's effect over time among those 11 to 18 years old, while accounting for the transition from whole-cell to acellular pertussis vaccines for the childhood primary series.
DESIGN, SETTING, AND PARTICIPANTS: Extended, retrospective analysis of reported pertussis cases between January 1, 1990, and December 31, 2014, in the United States. The analysis included all nationally reported pertussis cases.
US Tdap vaccination program and the transition from whole-cell to acellular pertussis vaccines.
Rate ratios of reported pertussis incidence (defined as incidence among 11- to 18-year-old individuals divided by the combined incidence in all other age groups) modeled with segmented regression analysis and age-specific trends in reported pertussis incidence over time.
Between 1990 and 2014, 356 557 pertussis cases were reported in the United States. Of those, 191 914 (53.8%) were female and 240 665 (67.5%) were white. Overall incidence increased from 1.7 in 100 000 to 4.0 in 100 000 between 1990 and 2003, while latter years were dominated by epidemic peaks. Incidence was highest among infants younger than 1 year throughout the analysis period. Pertussis rates were comparable among all other age groups until the late 2000s, when an increased burden of pertussis emerged among children 1 to 10 years old, resulting in the second highest age-specific incidence. By 2014, 11- to 18-year-old individuals once again had the second highest incidence. While slope coefficients from segmented regression analysis showed a positive impact of Tdap immediately following introduction (slope, -0.4959; P < .001), a reversal in trends was observed in 2010 when rates of disease among 11- to 18-year-old individuals increased at a faster rate than all other age groups combined (slope, 0.5727; P < .001).
While the impact of Tdap among adolescents looked promising following vaccine introduction, our extended analysis found that trends in adolescent disease were abruptly reversed in 2010, corresponding directly to the aging of acellular pertussis-vaccinated cohorts. Despite the apparent limitations of Tdap, it remains the best prevention against disease in adolescents.
越来越多的文献表明,无细胞百日咳疫苗诱导的免疫逐渐减弱,这证实了评估百白破疫苗保护持续时间的研究结果。
评估 11 至 18 岁人群中破伤风类毒素、白喉类毒素和无细胞百日咳(Tdap)疫苗的效果,同时考虑到儿童基础系列疫苗从全细胞到无细胞百日咳的转变。
设计、地点和参与者:在美国,1990 年 1 月 1 日至 2014 年 12 月 31 日期间报告的百日咳病例的扩展、回顾性分析。该分析包括所有全国性报告的百日咳病例。
美国 Tdap 疫苗接种计划和全细胞到无细胞百日咳疫苗的转变。
采用分段回归分析模型,计算报告的百日咳发病率比率(定义为 11 至 18 岁人群的发病率除以所有其他年龄组的发病率总和),以及随时间变化的报告的百日咳发病率的年龄特异性趋势。
1990 年至 2014 年间,美国报告了 356557 例百日咳病例。其中,女性 191914 例(53.8%),白人 240665 例(67.5%)。总体发病率从 1990 年至 2003 年期间的每 100000 人 1.7 例上升至每 100000 人 4.0 例,而近年来则以疫情高峰为主。在整个分析期间,发病率在 1 岁以下的婴儿中最高。在 2000 年代后期,所有其他年龄组的百日咳发病率相当,1 至 10 岁儿童的百日咳负担增加,导致第二个年龄组的发病率最高。到 2014 年,11 至 18 岁人群再次成为第二高发病率人群。虽然分段回归分析的斜率系数显示 Tdap 在引入后立即产生了积极影响(斜率为-0.4959;P<0.001),但在 2010 年,11 至 18 岁人群的疾病发病率增长速度快于所有其他年龄组的发病率增长速度(斜率为 0.5727;P<0.001),这种趋势发生了逆转。
虽然 Tdap 在疫苗引入后对青少年的影响看起来很有希望,但我们的扩展分析发现,2010 年青少年疾病的趋势突然逆转,这与无细胞百日咳疫苗接种人群的老龄化直接相关。尽管 Tdap 存在明显的局限性,但它仍然是预防青少年疾病的最佳方法。