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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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Insights into the limited global spread of the immune evasive SARS-CoV-2 variant Mu

TL;DR: This study demonstrates that, although Mu is less sensitive to neutralization compared to variants that preceded it, it did not spread significantly outside of South and Central America, and suggests that immune evasion alone was not sufficient to outcompete highly transmissible variants that were circulating concurrently with Mu.
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Game of transmissions (GoT) of SARS-CoV-2: Second wave of COVID-19 is here in India

TL;DR: In this paper , the authors analyse the past development about SARS-CoV-2 transmission pathway related recommendation(s) provided by WHO and track the trajectory to alert all the concerning stakeholders and policymakers to rethink and to collect adequate scientific data before they recommend or neglect any specific or all the possible transmission pathways to control the spread of infectious agents further.
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Cross-reactive SARS-CoV-2 epitope targeted across donors informs immunogen design

TL;DR: In this article , the authors identify cross-reactive antibodies from diverse gene rearrangements targeting two conserved receptor-binding domain epitopes and show that an engineered immunogen enriches antibody responses to one of these conserved epitopes in mice with pre-existing SARS-CoV-2 immunity; elicited responses neutralize SARS, CoV2, variants, and related sarbecoviruses.
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A low dose of RBD and TLR7/8 agonist displayed on influenza virosome particles protects rhesus macaque against SARS-CoV-2 challenge

TL;DR: In this article , a COVID-19 virosome-based vaccine containing a low dose of RBD protein (15 µg) and the adjuvant 3M-052 (1 µg), displayed together on virosomes, was evaluated in non-human primates with two intramuscular administrations at week 0 and 4 and challenged with SARS-CoV-2 at week 8.
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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