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Multiple SARS-CoV-2 variants escape neutralization by vaccine-induced humoral immunity.

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TLDR
In this article, the authors evaluated the neutralization potency of 99 individuals that received one or two doses of either BNT162b2 or mRNA-1273 vaccines against pseudoviruses representing 10 globally circulating strains of SARS-CoV-2.
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This article is published in Cell.The article was published on 2021-04-29 and is currently open access. It has received 1109 citations till now. The article focuses on the topics: Vaccination & Humoral immunity.

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Longitudinal analysis of SARS-CoV-2 spike and RNA-dependent RNA polymerase protein sequences reveals the emergence and geographic distribution of diverse mutations

TL;DR: In this article , a structural analysis was performed to investigate mutations in the receptor binding domain and the N-terminal domain of the spike protein and the RNA dependent RNA polymerase complex proteins.
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A bivalent nanoparticle vaccine exhibits potent cross-protection against the variants of SARS-CoV-2

TL;DR: In this paper , a bivalent nanoparticle vaccine that displays the receptor binding domains (RBDs) of the D614G and B.1.351 strains was developed to prevent SARS-CoV-2 infection.
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The Evolving Faces of the SARS-CoV-2 Genome.

TL;DR: This paper applied molecular portrayal using self-organizing maps machine learning (SOM portrayal) to characterize the diversity of the virus genomes, their mutual relatedness and development since the beginning of the pandemic.
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Discovery of Small Molecule Entry Inhibitors Targeting the Fusion Peptide of SARS-CoV-2 Spike Protein

TL;DR: In this paper, the structural dynamics of the SARS-CoV-2 S protein at the fusion peptide (FP) domain and small molecule binding for therapeutics development were investigated.
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SARS-CoV-2-specific T cell immunity in cases of COVID-19 and SARS, and uninfected controls.

TL;DR: Infection with betacoronaviruses induces multi-specific and long-lasting T cell immunity against the structural N protein, and SARS-CoV-2-reactive T cells were found in individuals who had recovered from SARS or COVID-19 and in unexposed donors, although with different patterns of immunoreactivity.
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