印度尼西亚巴厘岛登革热高发区原有交叉反应抗体对登革热周期性爆发的影响。

IF 2.5 4区 医学 Q3 VIROLOGY
Jean Claude Balingit , Dionisius Denis , Ryosuke Suzuki , Rahma Fitri Hayati , Mya Myat Ngwe Tun , Yuki Takamatsu , Sri Masyeni , R. Tedjo Sasmono , Kouichi Morita
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引用次数: 0

摘要

登革热病毒(DENV)的四种血清型可引起从轻微发烧到严重疾病的一系列疾病。了解这四种血清型之间的免疫学相互作用对于理解四种血清型共同流行地区疫情爆发时血清型转变的动态至关重要。因此,我们利用2022年印度尼西亚巴厘岛登革热疫情爆发期间从48名经实验室确诊的登革热患者身上采集的急性期血浆样本,评估了针对四种登革热病毒血清型的中和抗体和抗体依赖性增强反应。通过使用单轮感染性颗粒来专门研究作为抗体靶标的登革热病毒结构表面蛋白的免疫原性,我们发现既往可能有DENV-1感染史的个体对DENV-3继发感染的易感性增加,这归因于对DENV-3的中和活性有限的交叉反应抗体(几何平均50%中和滴度(GMNT50)= 47.6 ± 11.5)。这种易感性在体外也很明显,平均增强倍数为 28.4 ± 33.9。与其他血清型(DENV-1 GMNT50 = 678.1 ± 9.0;DENV-2 GMNT50 = 210.5 ± 8.7;DENV-4 GMNT50 = 95.14 ± 7.0)相比,DENV-3的中和滴度明显较低。我们证明,先前对一种血清型的免疫可提供对其他血清型的有限交叉保护,从而影响随后爆发的主要血清型。这些发现强调了登革热免疫的复杂性及其对疫苗设计和高流行地区传播动态的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of pre-existing cross-reactive antibodies on cyclic dengue outbreaks in the hyperendemic region of Bali, Indonesia

The four serotypes of the dengue virus (DENV) cause a range of diseases ranging from mild fever to severe conditions. Understanding the immunological interactions among the four serotypes is crucial in comprehending the dynamics of serotype shifting during outbreaks in areas where all four serotypes co-circulate. Hence, we evaluated the neutralizing antibody and antibody-dependent enhancement responses against the four DENV serotypes using acute-phase plasma samples collected from 48 laboratory-confirmed dengue patients during a dengue outbreak in Bali, Indonesia in 2022. Employing single-round infectious particles to exclusively investigate immunogenicity to the structural surface proteins of DENV, which are the targets of antibodies, we found that individuals with a probable prior history of DENV-1 infection exhibited increased susceptibility to secondary DENV-3 infection, attributed to cross-reactive antibodies with limited neutralizing activity against DENV-3 (geometric mean 50 % neutralization titer (GMNT50) = 47.6 ± 11.5). This susceptibility was evident in vitro, with a mean fold enhancement of 28.4 ± 33.9. Neutralization titers against DENV-3 were significantly lower compared to other serotypes (DENV-1 GMNT50 = 678.1 ± 9.0; DENV-2 GMNT50 = 210.5 ± 8.7; DENV-4 GMNT50 = 95.14 ± 7.0). We demonstrate that prior immunity to one serotype provides limited cross-protection against the other serotypes, influencing the dominant serotype in subsequent outbreaks. These findings underscore the complexity of dengue immunity and its implications for vaccine design and transmission dynamics in hyperendemic regions.

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来源期刊
Virus research
Virus research 医学-病毒学
CiteScore
9.50
自引率
2.00%
发文量
239
审稿时长
43 days
期刊介绍: Virus Research provides a means of fast publication for original papers on fundamental research in virology. Contributions on new developments concerning virus structure, replication, pathogenesis and evolution are encouraged. These include reports describing virus morphology, the function and antigenic analysis of virus structural components, virus genome structure and expression, analysis on virus replication processes, virus evolution in connection with antiviral interventions, effects of viruses on their host cells, particularly on the immune system, and the pathogenesis of virus infections, including oncogene activation and transduction.
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