Correction: Therapeutic treatment of hepatitis E virus infection in pigs with a neutralizing monoclonal antibody
Isabella Hrabal, Elmira Aliabadi, Sven Reiche, Saskia Weber, Cora M. Holicki, Laura Schmid, Christine Fast, Charlotte Schröder, Benjamin Gutjahr, Patrick Behrendt, Martin H. Groschup, Martin Eiden
Abstract
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
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Taxonomy
TopicsHepatitis Viruses Studies and Epidemiology
Correction to: Scientifc Reports 10.1038/s41598-025-95992-x, published online 28 March 2025
The original version of this Article contained an error in Figure 2, where panel (A) did not display correctly due to an inadvertent technical issue during production. The original Figure 2 and accompanying legend appear below.Fig. 2. The HEV treatment experiment in pigs. (A) Overview of the experimental design in the 5F6A1 treatment experiment. (B) Partial HEV capsid protein p239 ELISA using rabbit anti mouse antibody as secondary antibody for detection of applicated murine mAb 5F6A1. Samples were run in duplicates. Depicted are the means and standard error of measurements. (C) Partial HEV capsid protein p239 ELISA using protein G as the secondary antibody for detection of swine antibodies after infection. Samples were run in duplicates. (D) HEV-3 RNA in fecal samples, detected by RT-qPCR. (E) HEV-3 RNA in serum samples, detected by RT-qPCR. Note the different scaling of the y-axes in comparison to “D”. Bars depict mean values. Error bars depict the standard error. Box-and-whisker plots show mean and interquartile range.
The original Article has been corrected.