Lehmann D, Kakazo M, Saleu G, Taime J, Javati A, Namuigi P, Alpers M P, Wegmüller B, Zellmeyer M, Fürer E, Que J U, Herzog C
Papua New Guinea Institute of Medical Research, Goroka.
P N G Med J. 2001 Mar-Jun;44(1-2):6-16.
In view of high mortality and morbidity from Haemophilus influenzae type b (Hib) in young Papua New Guinean children, the incorporation of a Hib conjugate vaccine into a nationwide immunization program would be of major public health benefit.
We evaluated the safety and immunogenicity of a lyophilized and a liquid form of Hib polysaccharide-tetanus toxoid conjugate vaccines (PRP-T) given in the same syringe as diphtheria-tetanus-pertussis (DTP) vaccine to children in Goroka, Eastern Highlands Province. In Part 1 of the study 209 children were randomized to receive at ages 1, 2 and 3 months either DTP alone or a liquid formulation of DTP/PRP-T or lyophilized PRP-T dissolved in DTP suspension. A further 75 children were given the liquid DTP/PRP-T formulation at ages 2, 3 and 4 months (Part 2). 54 children aged 15-18 months were given a booster of the same preparation of PRP-T/DTP as they had received during Part 1. Blood for antibody assays was collected at enrolment, before (Part 1 only) and one month after the third dose, then just before and 3 weeks after the booster dose.
Follow-up to age of 12 months showed that PRP-T was safe with no evidence of impaired response to individual vaccine components when combined with DTP. Geometric mean titres (GMTs) of anti-PRP antibody before vaccination (n = 64, mean age 41 days), after 2 doses (mean age 99 days) and after 3 doses (mean age 132 days) of the lyophilized formulation were 0.21, 1.48 and 5.04 microg/ml, respectively, with 58% and 89% having anti-PRP antibody titres > or = 1.0 microg/ml after 2 and 3 doses, respectively. Anti-PRP antibody responses to the liquid Hib vaccine formulation were lower (GMT post-dose 3 = 0.48 microg/ml) than to the lyophilized formulation, but better responses were elicited from older children (Part 2; GMT post-dose 3 = 0.78 microg/ml, with 79% > or = 0.15 microg/ml). Both PRP-T preparations elicited excellent booster responses suggesting that children are likely to be protected if exposed to Hib infection.
Lyophilized PRP-T given together with DTP is safe and immunogenic when given to young infants. The liquid DTP/PRP-T formulation showed a lower immunogenicity than in earlier studies with this vaccine, which might have been due to exposure to low temperature during shipment or the younger age at immunization.
鉴于巴布亚新几内亚幼儿中b型流感嗜血杆菌(Hib)导致的高死亡率和高发病率,将Hib结合疫苗纳入全国免疫规划将带来重大公共卫生效益。
我们评估了冻干剂型和液体制型的Hib多糖-破伤风类毒素结合疫苗(PRP-T)与白喉-破伤风-百日咳(DTP)疫苗在同一注射器中联合接种给东高地省戈罗卡儿童的安全性和免疫原性。在研究的第1部分,209名儿童被随机分组,在1、2和3月龄时分别单独接种DTP,或接种DTP/PRP-T液体制剂,或接种溶解于DTP悬液中的冻干PRP-T。另外75名儿童在2、3和4月龄时接种液体制剂DTP/PRP-T(第2部分)。54名15 - 18月龄儿童接种与第1部分相同制剂的PRP-T/DTP加强针。在入组时、第3剂接种前(仅第1部分)和接种后1个月采集血液进行抗体检测,然后在加强针接种前和接种后3周采集血液。
随访至12月龄显示,PRP-T是安全的,与DTP联合使用时没有证据表明对各疫苗成分的免疫反应受损。冻干制剂在接种疫苗前(n = 64,平均年龄41天)、2剂接种后(平均年龄99天)和3剂接种后(平均年龄132天)的抗PRP抗体几何平均滴度(GMTs)分别为0.21、1.48和5.04μg/ml,2剂和3剂接种后分别有58%和89%的儿童抗PRP抗体滴度≥1.0μg/ml。液体制剂Hib疫苗的抗PRP抗体反应低于冻干制剂(第3剂接种后GMT = 0.48μg/ml),但年龄较大儿童的反应更好(第2部分;第3剂接种后GMT = 0.78μg/ml,79%≥0.15μg/ml)。两种PRP-T制剂均引发了良好的加强针反应,表明儿童如果接触Hib感染可能会受到保护。
冻干PRP-T与DTP联合给幼儿接种时是安全且具有免疫原性的。液体制剂DTP/PRP-T的免疫原性低于该疫苗早期研究中的结果,这可能是由于运输过程中暴露于低温或免疫接种时年龄较小所致。