Evidence map›Paper›PMID 37338118›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2023

Commercial Immunoglobulin Products Contain Neutralizing Antibodies Against Severe Acute Respiratory Syndrome Coronavirus 2 Spike Protein.

Vinit Upasani, Katie Townsend, Mary Y Wu, Edward J Carr, Agnieszka Hobbs, Giulia Dowgier, Martina Ragno, Lou S Herman, Sonal Sharma, Devesh Shah and 19 more

Open access · hybridAbstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
5.4field-weighted citation impact, top 3% of its field
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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

29 authors at 5 institutions in 1 country.

Vinit UpasaniInstitute of Immunity and Transplantation, University College London (UCL), London, United Kingdom.
Katie TownsendDepartment of Clinical Immunology, Royal Free London National Health Service (NHS) Foundation Trust, London, United Kingdom.
Mary Y WuCOVID Surveillance Unit, Francis Crick Institute, London, United Kingdom.
Edward J CarrFrancis Crick Institute, London, United Kingdom.
Agnieszka HobbsCOVID Surveillance Unit, Francis Crick Institute, London, United Kingdom.
Giulia DowgierCOVID Surveillance Unit, Francis Crick Institute, London, United Kingdom.
Martina RagnoCOVID Surveillance Unit, Francis Crick Institute, London, United Kingdom.
Lou S HermanCOVID Surveillance Unit, Francis Crick Institute, London, United Kingdom.
Sonal SharmaDepartment of Elderly Medicine, Barnet Hospital, Royal Free London NHS Foundation Trust, London, United Kingdom.
Devesh ShahDepartment of Elderly Medicine, Barnet Hospital, Royal Free London NHS Foundation Trust, London, United Kingdom.
Simon F K LeeDepartment of Infectious Diseases, Royal Free London NHS Foundation Trust, London, United Kingdom.
Neil ChauhanDepartment of Haematology, Royal Free London NHS Foundation Trust, London, United Kingdom.
Julie M GlanvilleDepartment of Haematology, Royal Free London NHS Foundation Trust, London, United Kingdom.
Lucy NeaveDepartment of Haematology, Royal Free London NHS Foundation Trust, London, United Kingdom.
Steven HansonDepartment of Haematology, Royal Free London NHS Foundation Trust, London, United Kingdom.
Sriram RavichandranDepartment of Haematology, Royal Free London NHS Foundation Trust, London, United Kingdom.
Aoife TynanDepartment of Pharmacy, Royal Free London NHS Foundation Trust, London, United Kingdom.
Mary O'SullivanDepartment of Clinical Immunology, Royal Free London National Health Service (NHS) Foundation Trust, London, United Kingdom.
Fernando MoreiraDepartment of Clinical Immunology, Royal Free London National Health Service (NHS) Foundation Trust, London, United Kingdom.
Sarita WorkmanDepartment of Clinical Immunology, Royal Free London National Health Service (NHS) Foundation Trust, London, United Kingdom.
Andrew SymesDepartment of Clinical Immunology, Royal Free London National Health Service (NHS) Foundation Trust, London, United Kingdom.
Siobhan O BurnsInstitute of Immunity and Transplantation, University College London (UCL), London, United Kingdom.
Susan TadrosDepartment of Clinical Immunology, Royal Free London National Health Service (NHS) Foundation Trust, London, United Kingdom.
Jennifer C L HartDepartment of Virology, Royal Free London NHS Foundation Trust, London, United Kingdom.
Rupert C L BealeCOVID Surveillance Unit, Francis Crick Institute, London, United Kingdom.
Sonia GandhiCOVID Surveillance Unit, Francis Crick Institute, London, United Kingdom.
Emma C WallCOVID Surveillance Unit, Francis Crick Institute, London, United Kingdom.
Laura McCoyInstitute of Immunity and Transplantation, University College London (UCL), London, United Kingdom.
David M LoweInstitute of Immunity and Transplantation, University College London (UCL), London, United Kingdom.
Royal Free London NHS Foundation Trust · GBThe Francis Crick Institute · GBUniversity College London · GBNational Health Service · GBThe Royal Free Hospital · GB

Funding

Medical Research Council MR/X006751/1
6 · The paper itself

Abstract

backgroundPatients with antibody deficiency respond poorly to coronavirus disease 2019 (COVID-19) vaccination and are at risk of severe or prolonged infection. They are given long-term immunoglobulin replacement therapy (IRT) prepared from healthy donor plasma to confer passive immunity against infection. Following widespread COVID-19 vaccination alongside natural exposure, we hypothesized that immunoglobulin preparations will now contain neutralizing severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike antibodies, which confer protection against COVID-19 disease and may help to treat chronic infection.

methodsWe evaluated anti-SARS-CoV-2 spike antibody in a cohort of patients before and after immunoglobulin infusion. Neutralizing capacity of patient samples and immunoglobulin products was assessed using in vitro pseudovirus and live-virus neutralization assays, the latter investigating multiple batches against current circulating Omicron variants. We describe the clinical course of 9 patients started on IRT during treatment of COVID-19.

resultsIn 35 individuals with antibody deficiency established on IRT, median anti-spike antibody titer increased from 2123 to 10 600 U/mL postinfusion, with corresponding increase in pseudovirus neutralization titers to levels comparable to healthy donors. Testing immunoglobulin products directly in the live-virus assay confirmed neutralization, including of BQ1.1 and XBB variants, but with variation between immunoglobulin products and batches.Initiation of IRT alongside remdesivir in patients with antibody deficiency and prolonged COVID-19 infection (median 189 days, maximum >900 days with an ancestral viral strain) resulted in clearance of SARS-CoV-2 at a median of 20 days.

conclusionsImmunoglobulin preparations now contain neutralizing anti-SARS-CoV-2 antibodies that are transmitted to patients and help to treat COVID-19 in individuals with failure of humoral immunity.

Indexed as

Antibodies, NeutralizingCOVID-19Antibodies, ViralCOVID-19 VaccinesHumansSARS-CoV-2Spike Glycoprotein, CoronavirusAntibodies, NeutralizingAntibodies, ViralCOVID-19 VaccinesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2immunodeficiencyIVIGneutralizationSARS-CoV-2spike antibody

Identifiers

PMID37338118
PMCPMC10552578
OpenAlexW4381309336

What OpenQuestion holds

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LicenceCC BY
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.