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用标准成熟病毒检测的登革病毒IgG和中和抗体滴度具有保护性。

Dengue virus IgG and neutralizing antibody titers measured with standard and mature viruses are protective.

作者信息

Odio Camila D, Daag Jedas Veronica, Crisostomo Maria Vinna, Voirin Charlie J, Coello Escoto Ana, Adams Cameron, Dahora Hein Lindsay, Aogo Rosemary A, Mpingabo Patrick I, Raimundi Rodriguez Guillermo, Firdous Saba, Abad Fernandez Maria, White Laura J, Agrupis Kristal An, Deen Jacqueline, de Silva Aravinda M, Ylade Michelle, Katzelnick Leah C

机构信息

Viral Epidemiology and Immunity Unit, Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.

Institute of Child Health and Human Development, National Institutes of Health, University of the Philippines Manila, Manila, Philippines.

出版信息

Nat Commun. 2025 Jan 2;16(1):191. doi: 10.1038/s41467-024-53916-9.

Abstract

The standard dengue virus (DENV) neutralization assay inconsistently predicts dengue protection. We compare how IgG ELISA, envelope domain III (EDIII), or non-structural protein 1 (NS1) binding antibodies, and titers from plaque reduction neutralization tests (PRNTs) using standard and mature viruses are associated with dengue. The ELISA measures IgG antibodies that bind to inactivated DENV1-4. The EDIII and NS1 assays measure binding antibodies, and the PRNTs measure neutralizing antibodies to each specific DENV serotype. Healthy children (n = 1206) in Cebu, Philippines were followed for 5 years. ELISA IgG≥3 was associated with reduced dengue probability relative to naïve children (3% vs. 10%, p = 0.007). Serotype-specific antibodies binding EDIII or NS1 had no association with dengue risk. Standard virus PRNT geometric mean titers (GMT) > 200 and mature GMT > 100 were associated with reduced dengue disease overall (p < 0.01). High DENV2 and DENV3 titers against either standard or mature viruses protected against the matched serotype (p < 0.01). While 43% of dengue cases had standard virus PRNT titers>100, only 2% of cases had mature virus PRNT titers>100 (p < 0.001), indicating a lower, more consistent threshold for protection. These assays may serve as correlates of protection.

摘要

标准的登革病毒(DENV)中和试验对登革热保护作用的预测并不一致。我们比较了IgG酶联免疫吸附测定(ELISA)、包膜结构域III(EDIII)或非结构蛋白1(NS1)结合抗体,以及使用标准病毒和成熟病毒的蚀斑减少中和试验(PRNT)的滴度与登革热之间的关联。ELISA检测与灭活的DENV1 - 4结合的IgG抗体。EDIII和NS1检测测量结合抗体,而PRNT检测针对每种特定DENV血清型的中和抗体。对菲律宾宿务的1206名健康儿童进行了为期5年的随访。相对于未感染儿童,ELISA IgG≥3与登革热发病概率降低相关(3%对10%,p = 0.007)。与EDIII或NS1结合的血清型特异性抗体与登革热风险无关。标准病毒PRNT几何平均滴度(GMT)>200以及成熟病毒GMT>100与总体登革热疾病减少相关(p<0.01)。针对标准病毒或成熟病毒的高DENV2和DENV3滴度可预防相应血清型的感染(p<0.01)。虽然43%的登革热病例标准病毒PRNT滴度>100,但只有2%的病例成熟病毒PRNT滴度>100(p<0.001),这表明保护阈值更低且更一致。这些检测方法可作为保护作用的相关指标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20e7/11697199/16377a075c91/41467_2024_53916_Fig1_HTML.jpg

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