First Experimental in Vivo Model of Enhanced Dengue Disease Severity Through Maternally Acquired Heterotypic Dengue Antibodies
Overview
Authors
Affiliations
Dengue (DEN) represents the most serious arthropod-borne viral disease. DEN clinical manifestations range from mild febrile illness to life-threatening hemorrhage and vascular leakage. Early epidemiological observations reported that infants born to DEN-immune mothers were at greater risk to develop the severe forms of the disease upon infection with any serotype of dengue virus (DENV). From these observations emerged the hypothesis of antibody-dependent enhancement (ADE) of disease severity, whereby maternally acquired anti-DENV antibodies cross-react but fail to neutralize DENV particles, resulting in higher viremia that correlates with increased disease severity. Although in vitro and in vivo experimental set ups have indirectly supported the ADE hypothesis, direct experimental evidence has been missing. Furthermore, a recent epidemiological study has challenged the influence of maternal antibodies in disease outcome. Here we have developed a mouse model of ADE where DENV2 infection of young mice born to DENV1-immune mothers led to earlier death which correlated with higher viremia and increased vascular leakage compared to DENV2-infected mice born to dengue naïve mothers. In this ADE model we demonstrated the role of TNF-α in DEN-induced vascular leakage. Furthermore, upon infection with an attenuated DENV2 mutant strain, mice born to DENV1-immune mothers developed lethal disease accompanied by vascular leakage whereas infected mice born to dengue naïve mothers did no display any clinical manifestation. In vitro ELISA and ADE assays confirmed the cross-reactive and enhancing properties towards DENV2 of the serum from mice born to DENV1-immune mothers. Lastly, age-dependent susceptibility to disease enhancement was observed in mice born to DENV1-immune mothers, thus reproducing epidemiological observations. Overall, this work provides direct in vivo demonstration of the role of maternally acquired heterotypic dengue antibodies in the enhancement of dengue disease severity and offers a unique opportunity to further decipher the mechanisms involved.
Progress and challenges in development of animal models for dengue virus infection.
Yuya W, Yuansong Y, Susu L, Chen L, Yong W, Yining W Emerg Microbes Infect. 2024; 13(1):2404159.
PMID: 39312399 PMC: 11423536. DOI: 10.1080/22221751.2024.2404159.
Severe disease during both primary and secondary dengue virus infections in pediatric populations.
Aggarwal C, Ahmed H, Sharma P, Reddy E, Nayak K, Singla M Nat Med. 2024; 30(3):670-674.
PMID: 38321219 DOI: 10.1038/s41591-024-02798-x.
Understanding antibody-dependent enhancement in dengue: Are afucosylated IgG1s a concern?.
Teo A, Tan H, Loy T, Chia P, Chua C PLoS Pathog. 2023; 19(3):e1011223.
PMID: 36996026 PMC: 10062565. DOI: 10.1371/journal.ppat.1011223.
Morrison A, Paz-Soldan V, Vazquez-Prokopec G, Lambrechts L, Elson W, Barrera P PLoS One. 2023; 18(2):e0273798.
PMID: 36730229 PMC: 9894416. DOI: 10.1371/journal.pone.0273798.
Vimentin Inhibits Dengue Virus Type 2 Invasion of the Blood-Brain Barrier.
Yu J, Li X, Zhou D, Liu X, He X, Huang S Front Cell Infect Microbiol. 2022; 12:868407.
PMID: 35433510 PMC: 9005901. DOI: 10.3389/fcimb.2022.868407.