Pichichero Michael E, Rennels Margaret B, Edwards Kathryn M, Blatter Mark M, Marshall Gary S, Bologa Monica, Wang Elaine, Mills Elaine
University of Rochester Medical Center, Rochester, NY 14642, USA.
JAMA. 2005 Jun 22;293(24):3003-11. doi: 10.1001/jama.293.24.3003. Epub 2005 Jun 2.
Increasing reports of pertussis among US adolescents, adults, and their infant contacts have stimulated vaccine development for older age groups.
To assess the immunogenicity and reactogenicity of a tetanus-diphtheria 5-component (pertussis toxoid, filamentous hemagglutinin, pertactin, and fimbriae types 2 and 3) acellular pertussis vaccine (Tdap) in adolescents and adults.
DESIGN, SETTING, AND PARTICIPANTS: A prospective, randomized, modified double-blind, comparative trial was conducted in healthy adolescents and adults aged 11 through 64 years from August 2001 to August 2002 at 39 US clinical centers.
A single 0.5-mL intramuscular dose of either Tdap or tetanus-diphtheria vaccine (Td).
Antibody titers to diphtheria and tetanus toxoids for Tdap and Td were measured in sera collected from subsets of adolescents and adults, before and 28 days after vaccination. For pertussis antigens, titers in sera from Tdap vaccinees were assessed vs those from infants who received analogous pediatric diphtheria-tetanus-acellular pertussis vaccine (DTaP) in a previous efficacy trial. Safety was assessed via solicited local and systemic reactions for 14 days and adverse events for 6 months following vaccination.
A total of 4480 participants were enrolled. For both Tdap and Td, more than 94% and nearly 100% of vaccinees had protective antibody concentrations of at least 0.1 IU/mL for diphtheria and tetanus, respectively. Geometric mean antibody titers to pertussis toxoid, filamentous hemagglutinin, pertactin, and fimbriae types 2 and 3 exceeded (by 2.1 to 5.4 times) levels in infants following immunization at 2, 4, and 6 months with DTaP. The incidence of solicited local and systemic reactions and adverse events was generally similar between the Tdap and Td groups.
This Tdap vaccine elicited robust immune responses in adolescents and adults to pertussis, tetanus, and diphtheria antigens, while exhibiting an overall safety profile similar to that of a licensed Td vaccine. These data support the potential routine use of this Tdap vaccine in adolescents and adults.
美国青少年、成年人及其婴儿接触者中百日咳报告病例不断增加,促使人们开发针对大龄人群的疫苗。
评估破伤风-白喉5组分(百日咳类毒素、丝状血凝素、百日咳杆菌黏附素以及2型和3型菌毛)无细胞百日咳疫苗(Tdap)在青少年和成年人中的免疫原性和反应原性。
设计、地点和参与者:2001年8月至2002年8月在美国39个临床中心对11至64岁的健康青少年和成年人进行了一项前瞻性、随机、改良双盲、对照试验。
单次肌内注射0.5 mL的Tdap或破伤风-白喉疫苗(Td)。
在青少年和成年人亚组接种疫苗前和接种后28天采集的血清中测量Tdap和Td针对白喉和破伤风类毒素的抗体滴度。对于百日咳抗原,将Tdap疫苗接种者血清中的滴度与先前一项疗效试验中接种类似儿科白喉-破伤风-无细胞百日咳疫苗(DTaP)的婴儿的血清滴度进行比较。通过接种疫苗后14天内主动报告的局部和全身反应以及6个月内的不良事件来评估安全性。
共纳入4480名参与者。对于Tdap和Td,分别有超过94%和近100%的疫苗接种者白喉和破伤风的保护性抗体浓度至少为0.1 IU/mL。针对百日咳类毒素、丝状血凝素、百日咳杆菌黏附素以及2型和3型菌毛的几何平均抗体滴度超过(2.1至5.4倍)婴儿在2、4和6个月接种DTaP后的水平。Tdap组和Td组主动报告的局部和全身反应以及不良事件的发生率总体相似。
这种Tdap疫苗在青少年和成年人中对白喉、破伤风和百日咳抗原引发了强烈的免疫反应,同时总体安全性与已获许可的Td疫苗相似。这些数据支持该Tdap疫苗在青少年和成年人中潜在的常规使用。