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The DOI matches its Crossref record; 78 of the 78 references it cites were found in a registry or an index.

COVID-19-neutralizing antibodies predict disease severity and survival

Open access
Garcia-Beltran, Wilfredo F., Lam, Evan C., Astudillo, Michael G., Yang, Diane, Miller, Tyler E., Feldman, Jared, Hauser, Blake M., Caradonna, Timothy M., Clayton, Kiera L., Nitido, Adam D., Murali, Mandakolathur R., Alter, Galit, Charles, Richelle C., Dighe, Anand, Branda, John A., Lennerz, Jochen K., Lingwood, Daniel, Schmidt, Aaron G., Iafrate, A. John, Balazs, Alejandro B.·2021·Cell

Published version of a preprint

Abstract

SUMMARY COVID-19 exhibits variable symptom severity ranging from asymptomatic to life-threatening, yet the relationship between severity and the humoral immune response is poorly understood. We examined antibody responses in 113 COVID-19 patients and found that severe cases resulting in intubation or death exhibited increased inflammatory markers, lymphopenia, pro-inflammatory cytokines, and high anti-RBD antibody levels. While anti-RBD IgG levels generally correlated with neutralization titer, quantitation of neutralization potency revealed that high potency was a predictor of survival. In addition to neutralization of wild-type SARS-CoV-2, patient sera were also able to neutralize the recently emerged SARS-CoV-2 mutant D614G, suggesting cross-protection from reinfection by either strain. However, SARS-CoV-2 sera generally lacked cross-neutralization to a highly-homologous pre-emergent bat coronavirus, WIV1-CoV, that has not yet crossed the species barrier. These results highlight the importance of neutralizing humoral immunity on disease progression and the need to develop broadly protective interventions to prevent future coronavirus pandemics.

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Research works printed but not linked: 4

  1. Du, 2010, Development of a safe and convenient neutralization assay for rapid screening of influenza HA-specific neutralizing monoclonal antibodies, Biochem. Biophys. Res. Commun., 397, 580, 10.1016/j.bbrc.2010.05.161 · doi:10.1016/j.bbrc.2010.05.161
  2. Mulligan, 2020, Phase I/II study of COVID-19 RNA vaccine BNT162b1 in adults, Nature, 586, 589, 10.1038/s41586-020-2639-4 · doi:10.1038/s41586-020-2639-4 · Paper page
  3. Ujike, 2016, The contribution of the cytoplasmic retrieval signal of severe acute respiratory syndrome coronavirus to intracellular accumulation of S proteins and incorporation of S protein into virus-like particles, J. Gen. Virol., 97, 1853, 10.1099/jgv.0.000494 · doi:10.1099/jgv.0.000494
  4. Zhou, 2020, SARS-CoV-2 Spike D614G Variant Confers Enhanced Replication and Transmissibility, bioRxiv

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Metadata

Authors
Garcia-Beltran, W. F., Lam, E. C., Astudillo, M. G., Yang, D., Miller, T. E., Feldman, J., Hauser, B. M., Caradonna, T. M., Clayton, K. L., Nitido, A. D., Murali, M. R., Alter, G., Charles, R. C., Dighe, A., Branda, J. A., Lennerz, J. K., Lingwood, D., Schmidt, A. G., Iafrate, A. J., & Balazs, A. B.
Venue
Cell
Publisher
Elsevier BV
Published
2021-01
Volume
184
Issue
2
Pages
476-488.e11
ISSN
0092-8674 (ISSN-L)
OpenAlex
W3113228067
Cited by
722
References
78
FWCI
17.17
Type
journal article
Language
en
Open access
bronze
Licence
Funders
  • Massachusetts General Hospital
  • Charles H. Hood Foundation
  • Gilead Sciences
  • National Institutes of Health

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Garcia-Beltran, W. F., Lam, E. C., Astudillo, M. G., Yang, D., Miller, T. E., Feldman, J., Hauser, B. M., Caradonna, T. M., Clayton, K. L., Nitido, A. D., Murali, M. R., Alter, G., Charles, R. C., Dighe, A., Branda, J. A., Lennerz, J. K., Lingwood, D., Schmidt, A. G., Iafrate, A. J., & Balazs, A. B. (2021). COVID-19-neutralizing antibodies predict disease severity and survival. Cell. https://doi.org/10.1016/j.cell.2020.12.015

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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