Lee Soyoung, Kim Han Wool, Lee Ji Hyen, Kim Kyung-Hyo
Center for Vaccine Evaluation and Study, Medical Research Institute, Ewha Womans University School of Medicine, Seoul, Republic of Korea.
Center for Vaccine Evaluation and Study, Medical Research Institute, Ewha Womans University School of Medicine, Seoul, Republic of Korea; Department of Pediatrics, Ewha Womans University School of Medicine, Seoul, Republic of Korea.
Vaccine. 2017 Sep 5;35(37):4960-4965. doi: 10.1016/j.vaccine.2017.07.074. Epub 2017 Aug 1.
The 23-valent pneumococcal polysaccharide vaccine (PPSV23) has been recommended for adults aged ≥65years. To evaluate functional immune response against the additional 11 serotypes that are included in PPSV23, but not the 13-valent pneumococcal conjugate vaccine (PCV13), serotype-specific anti-pneumococcal antibodies were examined using an opsonophagocytic assay (OPA).
Participants ≥65years of age that were naïve to the pneumococcal vaccine were enrolled. They were divided into two groups according to their age: group 1 (N=30; aged 65-74years) and group 2 (N=32; aged ≥75years). The functional antibody response prior to and 4weeks post-immunization with PPSV23 was determined, using a multiplexed OPA (MOPA) for 11 pneumococcal serotypes (2, 8, 9N, 10A, 11A, 12F, 15B, 17F, 20B, 22F, and 33F).
Geometric mean OPA titers (GMTs) to 11 serotypes were significantly increased in both groups post-immunization compared to those prior to immunization. The GMTs for all serotypes were not significantly different between the two groups after immunization. The proportion of subjects with OPA titers post-immunization of ≥8 and ≥64 was 93-100% and 80-100% for the 11 serotypes, respectively, while subjects with a ≥4-fold increase in OPA titers ranged from 9 to 90% for the 11 serotypes.
This study revealed that PPSV23 vaccination induced significant functional immune responses to 11 non-PCV13 serotypes in older adults. The MOPA has been shown to be a useful tool for future application in evaluating new PCVs in older adults. The clinical trial registration number is KCT 0001963 (CRIS, https://cris.nih.go.kr/cris/en/).
23价肺炎球菌多糖疫苗(PPSV23)已被推荐用于65岁及以上的成年人。为了评估针对PPSV23中包含但13价肺炎球菌结合疫苗(PCV13)中未包含的另外11种血清型的功能性免疫反应,使用吞噬杀菌试验(OPA)检测了血清型特异性抗肺炎球菌抗体。
纳入未接种过肺炎球菌疫苗的65岁及以上参与者。根据年龄将他们分为两组:第1组(N = 30;65 - 74岁)和第2组(N = 32;75岁及以上)。使用针对11种肺炎球菌血清型(2、8、9N、10A、11A、12F、15B、17F、20B、22F和33F)的多重OPA(MOPA)测定接种PPSV23前及接种后4周的功能性抗体反应。
与免疫前相比,两组免疫后针对11种血清型的几何平均OPA滴度(GMTs)均显著升高。免疫后两组所有血清型的GMTs无显著差异。免疫后OPA滴度≥8和≥64的受试者比例在11种血清型中分别为93 - 100%和80 - 100%,而OPA滴度增加≥4倍的受试者在11种血清型中为9 - 90%。
本研究表明,PPSV23疫苗接种可在老年人中诱导针对11种非PCV13血清型的显著功能性免疫反应。MOPA已被证明是未来用于评估老年人新型PCV的有用工具。临床试验注册号为KCT 0001963(CRIS,https://cris.nih.go.kr/cris/en/)。