Velumani Sumathy, Toh Ying Xiu, Balasingam Shobana, Archuleta Sophia, Leo Yee Sin, Gan Victor C, Thein Tun Linn, Wilder-Smith Annelies, Fink Katja
a Singapore Immunology Network, Agency for Science, Technology (A*STAR) , Singapore , Singapore.
b Lee Kong Chian School of Medicine, Nanyang Technological University , Singapore , Singapore.
Hum Vaccin Immunother. 2016 May 3;12(5):1265-73. doi: 10.1080/21645515.2015.1126012. Epub 2016 Feb 18.
Globally, dengue virus (DENV) is one of the most widespread vector-borne viruses. Dengue disease affects populations in endemic areas and, increasingly, tourists who travel to these countries, but there is currently no approved vaccine for dengue. A phase 3 efficacy trial with Sanofi-Pasteur's recombinant, live-attenuated, tetravalent dengue vaccine (CYD-TDV) conducted in South East Asia showed an overall efficacy of 56% against virologically confirmed dengue infections of any severity and any of the 4 serotypes, but the long-term protection of the vaccine has yet to be demonstrated. To address longevity of antibody titers and B cell memory, we recalled study participants from an earlier CYD immunogenicity study (Phase 2) conducted in Singapore that enrolled healthy volunteers in the year 2009. Depending on the age group, 57-84% of the participants initially generated a neutralizing antibody titer ≥ 10 to all 4 DENV serotypes 28 d after the third and final dose. We observed very low antibody titers in blood samples collected from 23 vaccinees 5 y after the first dose, particularly titers of antibodies binding to virus particles compared with those binding to recombinant E protein. The in vivo efficacy of plasma antibodies against DENV-2 challenge was also tested in a mouse model, which found that only 2 out of 23 samples were able to reduce viremia. Although the sample size is too small for general conclusions, dengue immune memory after vaccination with CYD-TDV appears relatively low.
在全球范围内,登革热病毒(DENV)是传播最广泛的媒介传播病毒之一。登革热疾病影响着流行地区的人群,并且越来越多地影响前往这些国家的游客,但目前尚无获批的登革热疫苗。赛诺菲-巴斯德公司的重组、减毒活、四价登革热疫苗(CYD-TDV)在东南亚进行的3期疗效试验显示,对任何严重程度和4种血清型中任何一种的病毒学确诊登革热感染的总体疗效为56%,但该疫苗的长期保护作用尚未得到证实。为了研究抗体滴度和B细胞记忆的持久性,我们从2009年在新加坡进行的一项早期CYD免疫原性研究(2期)中召回了研究参与者,该研究招募了健康志愿者。根据年龄组不同,57 - 84%的参与者在第三次也是最后一剂接种后28天,最初对所有4种DENV血清型产生的中和抗体滴度≥10。我们观察到,在首剂接种5年后从23名接种者采集的血样中抗体滴度非常低,特别是与结合重组E蛋白的抗体相比,结合病毒颗粒的抗体滴度更低。还在小鼠模型中测试了血浆抗体对DENV-2攻击的体内疗效,结果发现23个样本中只有2个能够降低病毒血症。尽管样本量过小无法得出一般性结论,但接种CYD-TDV后的登革热免疫记忆似乎相对较低。