de Barros Cardoso Cristina R, Cerqueira-Silva Thiago, Barral-Netto Manoel, Boaventura Viviane S
Department of Clinical Analysis, Toxicology and Food Sciences, School of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo (USP), Ribeirão Preto, Brazil.
Medicine and Precision Public Health Laboratory (MeSP2), Instituto Gonçalo Moniz, Fundação Oswaldo Cruz (Fiocruz), Salvador, Brazil.
Curr Top Microbiol Immunol. 2025 May 14. doi: 10.1007/82_2025_294.
This chapter examines the immunological mechanisms underlying the cross-reactivity and immune enhancement in dengue and how they influence the clinical outcomes. The four DENV serotypes (DENV-1 to DENV-4) share high genetic and antigenic similarity, leading to antibodies and T cells that can recognize multiple serotypes. While this cross-reactive immunity can confer partial or transient protection, it can also result in antibody-dependent enhancement (ADE), wherein non-neutralizing antibodies facilitate viral entry into immune cells, increasing the likelihood of severe disease in secondary infections and in infants carrying maternal anti-DENV antibodies. Furthermore, cross-reactivity with other flaviviruses, such as ZIKV, complicates serological diagnosis by producing false-positive results and uncertain prior exposure histories. These complexities extend to vaccine design, which must induce effective immunity against all four DENV serotypes while minimizing ADE risk. Epidemiological studies confirm that secondary infections, especially when antibody levels have waned, carry an elevated risk of severe clinical manifestations. However, the timing between infections and the specific serotype involved can modulate these outcomes. A thorough understanding of cross-reactivity and immune enhancement is therefore pivotal for advancing diagnostic accuracy, guiding patient care, and informing vaccine strategies and public health policies to better control dengue globally.
本章探讨登革热中交叉反应性和免疫增强背后的免疫机制,以及它们如何影响临床结果。四种登革病毒血清型(DENV-1至DENV-4)具有高度的遗传和抗原相似性,导致抗体和T细胞能够识别多种血清型。虽然这种交叉反应性免疫可以提供部分或短暂的保护,但它也可能导致抗体依赖性增强(ADE),即非中和性抗体促进病毒进入免疫细胞,增加二次感染以及携带母体抗登革病毒抗体的婴儿患严重疾病的可能性。此外,与其他黄病毒(如寨卡病毒)的交叉反应性会产生假阳性结果和不确定的既往暴露史,从而使血清学诊断变得复杂。这些复杂性延伸到疫苗设计,疫苗设计必须诱导针对所有四种登革病毒血清型的有效免疫,同时将ADE风险降至最低。流行病学研究证实,二次感染,尤其是当抗体水平下降时,会增加出现严重临床表现的风险。然而,感染之间的时间间隔和所涉及的特定血清型可以调节这些结果。因此,深入了解交叉反应性和免疫增强对于提高诊断准确性、指导患者护理以及为疫苗策略和公共卫生政策提供信息以更好地在全球范围内控制登革热至关重要。