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印度尼西亚巴厘岛高度流行地区既往交叉反应性抗体对周期性登革热暴发的影响。

Impact of pre-existing cross-reactive antibodies on cyclic dengue outbreaks in the hyperendemic region of Bali, Indonesia.

机构信息

Department of Tropical Viral Vaccine Development, Institute of Tropical Medicine, Nagasaki University, Nagasaki 852-8523, Japan.

Exeins Health Initiative (EHI), Jakarta 12870, Indonesia.

出版信息

Virus Res. 2024 Oct;348:199445. doi: 10.1016/j.virusres.2024.199445. Epub 2024 Aug 3.

DOI:10.1016/j.virusres.2024.199445
PMID:39089369
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11342788/
Abstract

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 (GMNT) = 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 GMNT = 678.1 ± 9.0; DENV-2 GMNT = 210.5 ± 8.7; DENV-4 GMNT = 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.

摘要

登革病毒(DENV)有四个血清型,可引起从轻度发热到严重疾病等一系列病症。了解这四个血清型之间的免疫相互作用对于理解在四个血清型同时流行的地区暴发期间血清型转变的动态至关重要。因此,我们评估了在 2022 年印度尼西亚巴厘岛登革热暴发期间,从 48 例经实验室确诊的登革热患者的急性期血浆样本中针对四个 DENV 血清型的中和抗体和抗体依赖性增强反应。我们使用单轮传染性颗粒,专门研究针对 DENV 结构表面蛋白的免疫原性,这些蛋白是抗体的靶标,发现有 DENV-1 既往感染史的个体对继发的 DENV-3 感染易感性增加,这归因于对 DENV-3 具有有限中和活性的交叉反应性抗体(几何平均 50%中和滴度(GMT)=47.6±11.5)。这种易感性在体外表现明显,平均增强倍数为 28.4±33.9。与其他血清型相比,针对 DENV-3 的中和滴度明显较低(DENV-1 GMT=678.1±9.0;DENV-2 GMT=210.5±8.7;DENV-4 GMT=95.14±7.0)。我们证明,对一个血清型的既往免疫提供了对其他血清型的有限交叉保护,影响随后暴发中的优势血清型。这些发现突显了登革热免疫的复杂性及其对疫苗设计和高度流行地区传播动态的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/133b/11342788/c8564c1f904c/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/133b/11342788/0b0b5748afd3/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/133b/11342788/b8a35a6a92ed/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/133b/11342788/c8564c1f904c/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/133b/11342788/0b0b5748afd3/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/133b/11342788/b8a35a6a92ed/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/133b/11342788/c8564c1f904c/gr3.jpg

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本文引用的文献

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Dengue Virus Serotype 4 Is Responsible for the Outbreak of Dengue in East Java City of Jember, Indonesia.
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