Evidence map›Paper›PMID 35262085›Full record

ArticlemedRxiv : the preprint server for health sciences2022

High Viral Specific Antibody Convalescent Plasma Effectively Neutralizes SARS-CoV-2 Variants of Concern.

Maggie Li, Evan J Beck, Oliver Laeyendecker, Yolanda Eby, Aaron Ar Tobian, Patrizio Caturegli, Camille Wouters, Gregory R Chiklis, William Block, Robert McKie and 25 more

Open access · greenAbstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

35 authors at 16 institutions in 1 country.

Maggie LiJohns Hopkins Bloomberg School of Public Health, Department of Molecular Microbiology and Immunology, Baltimore, MD.
Evan J BeckDivision of Intramural Research, National Institute of Allergy and Infectious Diseases, NIH.
Oliver LaeyendeckerDivision of Intramural Research, National Institute of Allergy and Infectious Diseases, NIH.
Yolanda EbyJohns Hopkins University School of Medicine, Department of Pathology, Baltimore, MD.
Aaron Ar TobianJohns Hopkins University School of Medicine, Department of Pathology, Baltimore, MD.
Patrizio CaturegliJohns Hopkins University School of Medicine, Department of Pathology, Baltimore, MD.
Camille WoutersJohns Hopkins Bloomberg School of Public Health, Department of Molecular Microbiology and Immunology, Baltimore, MD.
Gregory R ChiklisMRN Diagnostics, LLC Franklin, MA.
William BlockBlood Centers of America, West Warwick, RI.
Robert McKieInnovative Transfusion Medicine, Coral Springs, FL.
Michael JoynerDepartments of Anesthesiology and Perioperative Medicine, Mayo Clinic, Rochester, MN.
Timothy D WiltshireDepartment of Laboratory Medicine and Pathology, Division of Transfusion Medicine, Mayo Clinic, Rochester, MN.
Allan B DietzDepartment of Laboratory Medicine and Pathology, Division of Transfusion Medicine, Mayo Clinic, Rochester, MN.
Thomas J GniadekDepartment of Pathology, Northshore University Health System, Evanston, IL.
Arell ShapiroPathology, Hoag Hospital Newport Beach, CA.
Anusha YaravaJohns Hopkins University School of Medicine Department of Neurology, Brain Injury Outcomes Division, Baltimore, MD.
Karen LaneJohns Hopkins University School of Medicine Department of Neurology, Brain Injury Outcomes Division, Baltimore, MD.
Daniel HanleyJohns Hopkins University School of Medicine Department of Neurology, Brain Injury Outcomes Division, Baltimore, MD.
Evan M BlochJohns Hopkins University School of Medicine, Department of Pathology, Baltimore, MD.
Shmuel ShohamJohns Hopkins University School of Medicine, Department of Medicine, Division of Infectious Diseases, Baltimore, MD.
Edward R CachayDepartment of Medicine, Division of Infectious Diseases, University of California, San Diego, San Diego, CA.
Barry R MeisenbergLuminis Health, Annapolis, MD.
Moises A HuamanDepartment of Medicine, Division of Infectious Diseases, University of Cincinnati, Cincinnati, OH.
Yuriko FukutaDepartment of Medicine, Section of Infectious Diseases, Baylor College of Medicine, Houston, TX.
Bela PatelDepartment of Medicine, Divisions of Pulmonary and Critical Care Medicine, University of Texas Health Science Center, Houston, TX.
Sonya L HeathDepartment of Medicine, Division of Infectious Diseases, University of Alabama at Birmingham, Birmingham, AL.
Adam C LevineDepartment of Emergency Medicine, Rhode Island Hospital/Brown University, Providence, RI.
James H PaxtonDepartment of Emergency Medicine, Wayne State University, Detroit, MI.
Shweta AnjanDepartment of Medicine, Division of Infectious Diseases, University of Miami, Miller School of Medicine, Miami, FL.
Jonathan M GerberDepartment of Medicine, Division of Hematology and Oncology, University of Massachusetts Chan Medical School, Worcester, MA.
Kelly A GeboJohns Hopkins University School of Medicine, Department of Medicine, Division of Infectious Diseases, Baltimore, MD.
Arturo CasadevallJohns Hopkins Bloomberg School of Public Health, Department of Molecular Microbiology and Immunology, Baltimore, MD.
Andrew PekoszJohns Hopkins Bloomberg School of Public Health, Department of Molecular Microbiology and Immunology, Baltimore, MD.
David J SullivanJohns Hopkins Bloomberg School of Public Health, Department of Molecular Microbiology and Immunology, Baltimore, MD.
CSSC group
Johns Hopkins University · USMayo Clinic in Arizona · USNational Institute of Allergy and Infectious Diseases · USBaylor College of Medicine · USBrown University · USHoag Memorial Hospital Presbyterian · USInstitute for Transfusion Medicine · USMBio Diagnostics (United States) · USNorthShore University HealthSystem · USThe University of Texas Health Science Center at Houston · USUniversity of Alabama at Birmingham · USUniversity of California San Diego · USUniversity of Cincinnati · USUniversity of Massachusetts Chan Medical School · USUniversity of Miami · USWayne State University · US

Funding

QAQC Johns Hopkins Institute for Clinical and Translational ResearchUL1TR003098 · NCATS · JOHNS HOPKINS UNIVERSITY · PI FORD, DANIEL ERNEST · 2019 to 2023
$57.7M
Johns Hopkins-Tufts Trial Innovation Center HEAL Pain ERN SupplementU24TR001609 · NCATS · JOHNS HOPKINS UNIVERSITY · PI HANLEY, DANIEL F · 2016 to 2022
$36.3M
Conjugate vaccines for prevention and treatment of cryptococcosis - COVID-19 Revision SupplementR01AI152078 · NIAID · JOHNS HOPKINS UNIVERSITY · PI CASADEVALL, ARTURO · 2020 to 2024
$5.1M
NCATS NIH HHS U24 TR001609NCATS NIH HHS UL1 TR003098NIAID NIH HHS R01 AI152078
6 · The paper itself

Abstract

The ongoing evolution of SARS-Co-V2 variants to omicron severely limits available effective monoclonal antibody therapies. Effective drugs are also supply limited. Covid-19 convalescent plasma (CCP) qualified for high antibody levels effectively reduces immunocompetent outpatient hospitalization. The FDA currently allows outpatient CCP for the immunosuppressed. Viral specific antibody levels in CCP can range ten-to hundred-fold between donors unlike the uniform viral specific monoclonal antibody dosing. Limited data are available on the efficacy of polyclonal CCP to neutralize variants. We examined 108 pre-delta/pre-omicron donor units obtained before March 2021, 20 post-delta COVID-19/post-vaccination units and one pre-delta/pre-omicron hyperimmunoglobulin preparation for variant specific virus (vaccine-related isolate (WA-1), delta and omicron) neutralization correlated to Euroimmun S1 IgG antibody levels. We observed a 2-to 4-fold and 20-to 40-fold drop in virus neutralization from SARS-CoV-2 WA-1 to delta or omicron, respectively. CCP antibody levels in the upper 10% of the 108 donations as well as 100% of the post-delta COVID-19/post-vaccination units and the hyperimmunoglobulin effectively neutralized all three variants. High-titer CCP neutralizes SARS-CoV-2 variants despite no previous donor exposure to the variants. Key points: All of the post-delta COVID-19/post vaccination convalescent plasma effectively neutralizes the omicron and delta variants.High-titer CCP and hyperimmunoglobulin neutralizes SARS-CoV-2 variants despite no previous donor exposure to the variants.

Identifiers

PMID35262085
PMCPMC8902868
OpenAlexW4214912830

What OpenQuestion holds

Textmetadata
LicenceCC BY-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.