Ongoing evolution of SARS-CoV-2 drives escape from mRNA vaccine-induced humoral immunity

With the onset of the COVID-19 pandemic 4 years ago, viral sequencing continues to document numerous individual mutations in the viral spike protein across many variants. To determine the ability of vaccine-mediated humoral immunity to combat continued SARS-CoV-2 evolution, we construct a comprehensive panel of pseudoviruses harboring each individual mutation spanning 4 years of the pandemic to understand the fitness cost and resistance benefits of each. These efforts identify numerous mutations that escape from vaccine-induced humoral immunity. Across 50 variants and 131 mutants we construct, we observe progressive loss of neutralization across variants, irrespective of vaccine doses, as well as increasing infectivity and ACE2 binding. Importantly, the recent XBB.1.5 booster significantly increases titers against most variants but not JN.1, KP.2, or KP.3. These findings demonstrate that variants continue to evade updated mRNA vaccines, highlighting the need for different approaches to control SARS-CoV-2 transmission.

Authors

Institutions

Publication Details

Journal
Cell Reports Medicine
Published
2024-12-01
DOI
https://doi.org/10.1016/j.xcrm.2024.101850
Citations
13
Primary Topic
SARS-CoV-2 and COVID-19 Research
Type
article
Field-Weighted Citation Impact
5.06

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Ongoing evolution of SARS-CoV-2 drives escape from mRNA vaccine-induced humoral immunity

Evan C. Lam, Maegan L. Sheehan, Yi Cao, Kerri St. Denis et al.
13 citations
Cell Reports Medicine
SARS-CoV-2 and COVID-19 Research
5.06
article

Ongoing evolution of SARS-CoV-2 drives escape from mRNA vaccine-induced humoral immunity

Evan C. Lam, Maegan L. Sheehan, Yi Cao, Kerri St. Denis, Wilfredo F. García-Beltrán, A. John Iafrate, Stefan Gravenstein, David J. Gregory, Mark C. Poznansky, Alex Roederer, Alejandro B. Balazs, David H. Canaday, Chia Jung Li
article en
13 citations

Abstract

With the onset of the COVID-19 pandemic 4 years ago, viral sequencing continues to document numerous individual mutations in the viral spike protein across many variants. To determine the ability of vaccine-mediated humoral immunity to combat continued SARS-CoV-2 evolution, we construct a comprehensive panel of pseudoviruses harboring each individual mutation spanning 4 years of the pandemic to understand the fitness cost and resistance benefits of each. These efforts identify numerous mutations that escape from vaccine-induced humoral immunity. Across 50 variants and 131 mutants we construct, we observe progressive loss of neutralization across variants, irrespective of vaccine doses, as well as increasing infectivity and ACE2 binding. Importantly, the recent XBB.1.5 booster significantly increases titers against most variants but not JN.1, KP.2, or KP.3. These findings demonstrate that variants continue to evade updated mRNA vaccines, highlighting the need for different approaches to control SARS-CoV-2 transmission.

Cell Reports MedicineVol. 5(12)
Ragon Institute of MGH, MIT and Harvard (US), Providence VA Medical Center (US), Massachusetts General Hospital (US), Louis Stokes Cleveland VA Medical Center (US)
Coalition for Epidemic Preparedness Innovations, Massachusetts Consortium on Pathogen Readiness, Centers for Disease Control and Prevention, National Institute on Drug Abuse, National Institute of Allergy and Infectious Diseases
Zero hunger
Openalex Percentile: Top 4%
SARS-CoV-2 and COVID-19 Research
5.06
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.