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Image Search Results
Journal: bioRxiv
Article Title: The S2 subunit of spike encodes diverse targets for functional antibody responses to SARS-CoV-2
doi: 10.1101/2024.02.26.582219
Figure Lengend Snippet: Heatmap showing binding of mAbs from C68 and C20 (rows) to spike antigens by ELISAs. Spaces are colored based on the OD450nm values with higher numbers and more binding represented in darker green. Antigens (columns) included the following: SARS-CoV-2 WH-1 S2 subunit protein produced in mammalian cells (Mam) or insect cells (Ins), SARS-CoV-2 pre-fusion stabilized spike trimers from WH-1 and VOCs (Delta, Omicron VOCs BA.1, BA.2 BA.5, BQ.1.1, XBB), SARS-CoV-1, MERS-CoV, HCoV-HKU1, and MERS-CoV S2 monomer protein. All mAbs were tested at 1 μg/mL, except against the SARS-CoV-2 S2 protein the mAbs were tested at 1 μg/mL or 15 μg/mL as noted. Values were averaged over two technical replicates.
Article Snippet: The recombinant spike trimers used in these assays were as follows: Wuhan-Hu-1 (Sino Biological, cat. 40589-V08H4), Delta (Sino Biological, cat. 40589-V08H10),
Techniques: Binding Assay, Produced
Journal: bioRxiv
Article Title: The S2 subunit of spike encodes diverse targets for functional antibody responses to SARS-CoV-2
doi: 10.1101/2024.02.26.582219
Figure Lengend Snippet: (A) Screening of all S2 mAbs for neutralization of WH-1 spike-pseudotyped lentiviruses. All antibodies were tested at 10 μg/mL and the target cells were ACE2-expressing HEK293T cells. The percent neutralization of the pseudoviruses is shown, averaged across two technical replicates. One mAb, C20.119, was able to neutralize greater than 50%, which was the threshold for further assessment, shown by the dashed line. Neutralization of a panel of SARS-CoV-2 variant pseudoviruses (B) or sarbecovirus pseudoviruses (C) by C20.119. SARS-CoV-2 pseudoviruses tested included WH-1, Delta, Omicron VOCs BA.1, BA.2, BA.5, BQ.1.1, XBB, XBB.1.5. The related sarbecovirus pseudoviruses assessed were SARS-CoV-1, bat viruses RsSHC014 and WIV1, and Pangolin-GD. C20.119 was tested in 12-point dilution curves starting at 20 μg/mL for WH-1 and Delta and 80 μg/mL for the other pseudoviruses. Fraction infectivity values are the average of two technical replicates in two to three independent experiments using at least two pseudovirus batches. (D) Pseudovirus neutralization IC50 values for C20.119.
Article Snippet: The recombinant spike trimers used in these assays were as follows: Wuhan-Hu-1 (Sino Biological, cat. 40589-V08H4), Delta (Sino Biological, cat. 40589-V08H10),
Techniques: Neutralization, Expressing, Variant Assay, Infection
Journal: medRxiv
Article Title: Systems biological assessment of the temporal dynamics of immunity to a viral infection in the first weeks and months of life
doi: 10.1101/2023.01.28.23285133
Figure Lengend Snippet: Memory B and T cell response, related to A) Gating strategy used for SARS-CoV-2 spike specific IgG+ memory B cell staining and single-cell sorting. Gating was on singlets that were CD20+ and CD3-CD14-IgM-IgD-CD27low/+ IgG+. Sorted cells were Wuhan spike-AlexaFluor 488+ and/or Omicron spike-BV421+. B) The percentage of SARS-CoV-2 spike-specific IgG+ memory B cells in healthy, acute, and convalescent infant individuals. The sample number for each group is indicated in brackets. C) As in (B), the percentage of SARS-CoV-2 spike-specific IgG+ memory B cells in adult individuals with mild, severe, and ICU symptoms and in adult convalescent individuals. The sample number for each group is indicated in brackets. D-F) T cells were stimulated with overlapping peptides against WT (D-F) and Omicron (F) variants. Cytokine production was determined via flow cytometry. D) Box plot showing the fraction of responding T cells at different infection stages. E) Box plot showing the fraction of multifunctional T cells at different infection stages. F) Comparison of the multifunctional T cell response after stimulation with WT and Omicron (Om) peptides. Statistical comparisons were conducted with Wilcoxon rank sum test. Solid line indicates median healthy response; dashed line indicates 3x median healthy response.
Article Snippet: The following antibodies were used: IgD PE (BD Biosciences, 555779), IgM PerCP-Cy5.5 (BioLegend, 314512), CD20 APC-H7 (BD Biosciences, 560734), CD27 PE-Cy7 (BioLegend, 302838), CD14 PE/Dazzle™ 594 (BioLegend, 301852), CD16 BV605 (BioLegend, 302040), IgG BV650 (BD Biosciences, 740596), CD3 BUV737 (BD Biosciences, 612750) and Alexa Fluor 488-labeled Wuhan spike (SinoBiological, 40589-V27B-B), and
Techniques: Staining, FACS, Flow Cytometry, Infection