Significantly Decreased Mortality in a Large Cohort of Coronavirus Disease 2019 (COVID-19) Patients Transfused Early with Convalescent Plasma Containing High-Titer Anti-Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Spike Protein IgG.


Journal

The American journal of pathology
ISSN: 1525-2191
Titre abrégé: Am J Pathol
Pays: United States
ID NLM: 0370502

Informations de publication

Date de publication:
01 2021
Historique:
received: 02 10 2020
revised: 23 10 2020
accepted: 28 10 2020
pubmed: 7 11 2020
medline: 5 1 2021
entrez: 6 11 2020
Statut: ppublish

Résumé

Coronavirus disease 2019 (COVID-19) convalescent plasma has emerged as a promising therapy and has been granted Emergency Use Authorization by the US Food and Drug Administration for hospitalized COVID-19 patients. We recently reported results from interim analysis of a propensity score-matched study suggesting that early treatment of COVID-19 patients with convalescent plasma containing high-titer anti-spike protein receptor binding domain (RBD) IgG significantly decreases mortality. We herein present results from a 60-day follow-up of a cohort of 351 transfused hospitalized patients. Prospective determination of enzyme-linked immunosorbent assay anti-RBD IgG titer facilitated selection and transfusion of the highest titer units available. Retrospective analysis by the Ortho VITROS IgG assay revealed a median signal/cutoff ratio of 24.0 for transfused units, a value far exceeding the recent US Food and Drug Administration-required cutoff of 12.0 for designation of high-titer convalescent plasma. With respect to altering mortality, our analysis identified an optimal window of 44 hours after hospitalization for transfusing COVID-19 patients with high-titer convalescent plasma. In the aggregate, the analysis confirms and extends our previous preliminary finding that transfusion of COVID-19 patients soon after hospitalization with high-titer anti-spike protein RBD IgG present in convalescent plasma significantly reduces mortality.

Identifiants

pubmed: 33157066
pii: S0002-9440(20)30489-2
doi: 10.1016/j.ajpath.2020.10.008
pmc: PMC7609241
pii:
doi:

Substances chimiques

Antibodies, Neutralizing 0
Antibodies, Viral 0
Immunoglobulin G 0
Spike Glycoprotein, Coronavirus 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

90-107

Informations de copyright

Copyright © 2021 American Society for Investigative Pathology. Published by Elsevier Inc. All rights reserved.

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Auteurs

Eric Salazar (E)

Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas; Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York.

Paul A Christensen (PA)

Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas.

Edward A Graviss (EA)

Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas; Center for Molecular and Translational Human Infectious Diseases, Houston Methodist Research Institute, Houston, Texas.

Duc T Nguyen (DT)

Center for Molecular and Translational Human Infectious Diseases, Houston Methodist Research Institute, Houston, Texas.

Brian Castillo (B)

Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas.

Jian Chen (J)

Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas.

Bevin V Lopez (BV)

Academic Office of Clinical Trials, Houston Methodist Research Institute, Houston, Texas.

Todd N Eagar (TN)

Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas; Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York.

Xin Yi (X)

Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas; Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York.

Picheng Zhao (P)

Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas.

John Rogers (J)

Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas.

Ahmed Shehabeldin (A)

Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas.

David Joseph (D)

Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas.

Faisal Masud (F)

Department of Anesthesiology and Critical Care, Houston Methodist Hospital, Houston, Texas.

Christopher Leveque (C)

Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas.

Randall J Olsen (RJ)

Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas; Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York; Center for Molecular and Translational Human Infectious Diseases, Houston Methodist Research Institute, Houston, Texas.

David W Bernard (DW)

Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas; Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York.

Jimmy Gollihar (J)

The Combat Capabilities Development Command Army Research Laboratory-South, University of Texas at Austin, Austin, Texas.

James M Musser (JM)

Department of Pathology and Genomic Medicine, Houston Methodist Hospital, Houston, Texas; Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York; Center for Molecular and Translational Human Infectious Diseases, Houston Methodist Research Institute, Houston, Texas. Electronic address: jmmusser@houstonmethodist.org.

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Classifications MeSH