Utility of an In-Vitro Micro-Neutralizing Test in Comparison to a Plaque Reduction Neutralization Test for Dengue Virus, Japanese Encephalitis Virus, and Zika Virus Serology and Drug Screening.
Kazumi HagaZhenying Nancy ChenMisao HimenoRyuichi MajimaMeng Ling MoiPublished in: Pathogens (Basel, Switzerland) (2023)
Flavivirus infections, including dengue virus (DENV), Japanese encephalitis virus (JEV), and Zika virus (ZIKV), present significant global public health challenges. For successful vaccine design, the assessment of neutralizing antibody activity requires reliable and robust methodologies for determining antibody titers. Although the plaque reduction neutralization test (PRNT) is commonly acknowledged as the gold standard, it has limitations in terms of time and cost, and its usage may be limited in resource-limited settings. To address these challenges, we introduced the micro-neutralization test (MNT) as a simplified alternative to the PRNT. The MNT employs a 96-well plate format, conducts microscale neutralization assays, and assesses cell viability by dissolving cells to create a uniform color solution, which is measured with a spectrometer. In this study, we evaluated the utility of the MNT by contrasting the end-point titers of the MNT and PRNT using 4 monoclonal antibodies, 15 non-human primate serum samples, and 2 therapeutic drug candidates across flaviviruses. The results demonstrated a strong correlation between the MNT and PRNT titers, affirming the robustness and reproducibility of the MNT for evaluating control measures against flaviviruses. This research contributes valuable insights toward the development of a cost-effective antibody titer testing approach that is particularly suitable for resource-limited settings.
Keyphrases
- dengue virus
- zika virus
- aedes aegypti
- public health
- coronary artery disease
- endothelial cells
- induced apoptosis
- emergency department
- high throughput
- cell cycle arrest
- signaling pathway
- mass spectrometry
- induced pluripotent stem cells
- cell proliferation
- clinical evaluation
- pluripotent stem cells
- drug induced
- single cell
- disease virus
- silver nanoparticles
- solid state