ArticleRevista do Instituto de Medicina Tropical de Sao Paulo2026
Occlusion body-incorporated SARS-CoV-2 S-RBD via cypovirus polyhedrin-derived peptide: a novel insect cell-expressed antigen for high-accuracy COVID-19 diagnosis, and humoral immune response and hybrid immunity evaluation.
Article in Revista do Instituto de Medicina Tropical de Sao Paulo, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Accurate serological assays are critical for monitoring antibody responses to SARS-CoV-2 and for assessing vaccine efficacy. In this study, we engineered a recombinant baculovirus to express the SARS-CoV-2 spike receptor-binding domain (RBD) fused to an N-terminal peptide of cypovirus polyhedrin (S-RBD-POLH), thereby enabling its potential encapsulation within occlusion bodies. The construct was expressed in insect cells and employed to establish an in-house enzyme-linked immunosorbent assay (ELISA-S) for COVID-19 diagnosis and evaluation of the humoral immune response to SARS-CoV-2. We compared the performance of ELISA-S with a commercial lateral flow immunoassay (LFIA), a chemiluminescence immunoassay (CLIA), and an in-house ELISA targeting Escherichia coli-produced nucleocapsid (N) protein (ELISA-N). Both in-house ELISAs had excellent diagnostic performance (overall accuracy = 0.90), with ELISA-S achieving 98.9% sensitivity and 100% specificity. Inter-assay concordance was high (kappa coefficient > 0.92), with near-perfect agreement between ELISA-S and LFIA (kappa = 0.99). Longitudinal analysis revealed increasing anti-RBD IgG titers over time, in contrast to declining anti-N IgG levels, consistent with expected post-infection kinetics. Moreover, ELISA-S reliably detected antibodies in individuals with hybrid immunity across different periods of the pandemic. These findings establish a scalable platform for antigen encapsulation and production in insect cells to enhance antibody detection. The ELISA-S system represents a robust and adaptable approach for evaluating humoral immunity following infection, vaccination, or hybrid immunity, and can be used for all variants.
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