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Convalescent plasma with a high level of virus-specific antibody effectively neutralizes SARS-CoV-2 variants of concern.
Li, Maggie; Beck, Evan J; Laeyendecker, Oliver; Eby, Yolanda; Tobian, Aaron A R; Caturegli, Patrizio; Wouters, Camille; Chiklis, Gregory R; Block, William; McKie, Robert O; Joyner, Michael J; Wiltshire, Timothy D; Dietz, Allan B; Gniadek, Thomas J; Shapiro, Arell J; Yarava, Anusha; Lane, Karen; Hanley, Daniel F; Bloch, Evan M; Shoham, Shmuel; Cachay, Edward R; Meisenberg, Barry R; Huaman, Moises A; Fukuta, Yuriko; Patel, Bela; Heath, Sonya L; Levine, Adam C; Paxton, James H; Anjan, Shweta; Gerber, Jonathan M; Gebo, Kelly A; Casadevall, Arturo; Pekosz, Andrew; Sullivan, David J.
  • Li M; Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.
  • Beck EJ; Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health (NIH), Bethesda, MD.
  • Laeyendecker O; Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health (NIH), Bethesda, MD.
  • Eby Y; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD.
  • Tobian AAR; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD.
  • Caturegli P; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD.
  • Wouters C; Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.
  • Chiklis GR; Medical Research Network Diagnostics, Limited Liability Corporation, Franklin, MA.
  • Block W; Blood Centers of America, West Warwick, RI.
  • McKie RO; Innovative Transfusion Medicine, Coral Springs, FL.
  • Joyner MJ; Department of Anesthesiology and Perioperative Medicine, Mayo Clinic, Rochester, MN.
  • Wiltshire TD; Division of Transfusion Medicine, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN.
  • Dietz AB; Division of Transfusion Medicine, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN.
  • Gniadek TJ; Department of Pathology, Northshore University Health System, Evanston, IL.
  • Shapiro AJ; Department of Pathology, Hoag Hospital, Newport Beach, CA.
  • Yarava A; Brain Injury Outcomes Division, Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD.
  • Lane K; Brain Injury Outcomes Division, Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD.
  • Hanley DF; Brain Injury Outcomes Division, Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD.
  • Bloch EM; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD.
  • Shoham S; Division of Infectious Diseases, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD.
  • Cachay ER; Division of Infectious Diseases, Department of Medicine, University of California, San Diego, CA.
  • Meisenberg BR; Luminis Health, Annapolis, MD.
  • Huaman MA; Division of Infectious Diseases, Department of Medicine, University of Cincinnati, Cincinnati, OH.
  • Fukuta Y; Section of Infectious Diseases, Department of Medicine, Baylor College of Medicine, Houston, TX.
  • Patel B; Divisions of Pulmonary and Critical Care Medicine, Department of Medicine, University of Texas Health Science Center, Houston, TX.
  • Heath SL; Division of Infectious Diseases, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL.
  • Levine AC; Department of Emergency Medicine, Rhode Island Hospital/Brown University, Providence, RI.
  • Paxton JH; Department of Emergency Medicine, Wayne State University, Detroit, MI.
  • Anjan S; Division of Infectious Diseases, Department of Medicine, University of Miami, Miller School of Medicine, Miami, FL; and.
  • Gerber JM; Division of Hematology and Oncology, Department of Medicine, University of Massachusetts Chan Medical School, Worcester, MA.
  • Gebo KA; Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health (NIH), Bethesda, MD.
  • Casadevall A; Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.
  • Pekosz A; Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.
  • Sullivan DJ; Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.
Blood Adv ; 6(12): 3678-3683, 2022 06 28.
Article in English | MEDLINE | ID: covidwho-1799125
ABSTRACT
The ongoing evolution of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants 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 Food and Drug Administration currently allows outpatient CCP for the immunosuppressed. Viral-specific antibody levels in CCP can range 10- to 100-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-δ/pre-ο donor units obtained before March 2021, 20 post-δ COVID-19/postvaccination units, and 1 pre-δ/pre-ο hyperimmunoglobulin preparation for variant-specific virus (vaccine-related isolate [WA-1], δ, and ο) neutralization correlated to Euroimmun S1 immunoglobulin G antibody levels. We observed a two- to fourfold and 20- to 40-fold drop in virus neutralization from SARS-CoV-2 WA-1 to δ or ο, respectively. CCP antibody levels in the upper 10% of the 108 donations as well as 100% of the post-δ COVID-19/postvaccination units and the hyperimmunoglobulin effectively neutralized all 3 variants. High-titer CCP neutralizes SARS-CoV-2 variants despite no previous donor exposure to the variants.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Experimental Studies Topics: Vaccines / Variants Limits: Humans Country/Region as subject: North America Language: English Journal: Blood Adv Year: 2022 Document Type: Article Affiliation country: Bloodadvances.2022007410

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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Experimental Studies Topics: Vaccines / Variants Limits: Humans Country/Region as subject: North America Language: English Journal: Blood Adv Year: 2022 Document Type: Article Affiliation country: Bloodadvances.2022007410