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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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Differential T cell immunity to SARS-CoV-2 in mRNA-1273 and BNT162b2 vaccinated individuals.

TL;DR: It is demonstrated that anti-spike T-cell responses and IgG antibody levels are maintained but decrease over time and are lower in the BNT162b2- versus mRNA-1273-vaccinated individuals.
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Scope of SARS-CoV-2 variants, mutations, and vaccine technologies

TL;DR: In this paper , a review on the SARS-CoV-2 mutations, variants of concern (VOCs), and advances in vaccine technologies is presented, focusing on the Omicron variant, which has 32 mutations in its spike protein.
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Kappa-RBD produced by glycoengineered Pichia pastoris elicited high neutralizing antibody titers against pseudoviruses of SARS-CoV-2 variants

TL;DR: In this article , a glycoengineered Pichia pastoris expression system was used to prepare recombinant kappa-RBD candidate vaccine, which has sufficient potency to be a promising COVID-19 vaccine candidate.
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Rapidly identifying new coronavirus mutations of potential concern in the Omicron variant using an unsupervised learning strategy

TL;DR: In this paper , an unsupervised machine learning approach was applied to 4296 Omicron viral genomes collected and deposited to GISAID as of December 14, 2021, and identified a core haplotype of 28 polymutants (A67V, T95I, G339D, R346K, S371L, S373P, S375F, K417N, N440K, G446S, S477N, T478K, E484A, Q493R, G496S, Q498R, N501Y, Y505H, T547K, D614G, N679K, P681H, N764K, K796Y, N856K, Q954H, Q701, N69K, L981F).
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Large-Scale Identification of T-Cell Epitopes Derived From Severe Acute Respiratory Syndrome Coronavirus 2 for the Development of Peptide Vaccines Against Coronavirus Disease 2019.

TL;DR: Wang et al. as discussed by the authors presented an alternative and effective strategy for the identification of T-cell epitopes of SARS-CoV-2 in healthy subjects, which may indicate an important role in the development of peptide vaccines for COVID-19.
References
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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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