Evidence map›Paper›PMID 36211396›Full record

ArticleFrontiers in immunology2022

Impact of vaccination on hospitalization and mortality from COVID-19 in patients with primary and secondary immunodeficiency: The United Kingdom experience.

Adrian M Shields, Susan Tadros, Adam Al-Hakim, Jeremy M Nell, Me Me Nay Lin, Michele Chan, Sarah Goddard, John Dempster, Magdalena Dziadzio, Smita Y Patel and 13 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 6% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
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  4. Article
  5. Review
  6. Article
  7. Article
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  13. Commercial Immunoglobulin Products Contain Neutralizing Antibodies Against Severe Acute Respiratory Syndrome Coronavirus 2 Spike Protein.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2023
    Article
  14. Review
  15. Article
  16. Article
  17. Impact of Severe Acute Respiratory Syndrome Coronavirus 2 Variants on Inpatient Clinical Outcome.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2023
    Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors at 10 institutions in 1 country.

Adrian M ShieldsClinical Immunology Service, Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, United Kingdom.
Susan TadrosDepartment of Immunology, Royal Free London National Health Service (NHS) Foundation Trust, London, United Kingdom.
Adam Al-HakimDepartment of Allergy and Clinical Immunology, Leeds Teaching Hospitals National Health Service (NHS) Trust, Leeds, United Kingdom.
Jeremy M NellDepartment of Infection and Tropical Medicine, Newcastle upon Tyne Hospitals National Health Service (NHS) Foundation Trust and Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.
Me Me Nay LinDepartment of Immunology, Royal Free London National Health Service (NHS) Foundation Trust, London, United Kingdom.
Michele ChanDepartment of Immunology, Royal Free London National Health Service (NHS) Foundation Trust, London, United Kingdom.
Sarah GoddardDepartment of Clinical Immunology, University Hospitals North Midlands, Stoke-on-Trent, United Kingdom.
John DempsterDepartment of Clinical Immunology, University College London Hospital National Health Service (NHS) Foundation Trust, London, United Kingdom.
Magdalena DziadzioDepartment of Clinical Immunology, University College London Hospital National Health Service (NHS) Foundation Trust, London, United Kingdom.
Smita Y PatelNational Institute for Health and Care Research (NIHR) Biomedical Research Centre (BRC) Oxford Biomedical Centre, University of Oxford, Oxford, United Kingdom.
Shuayb ElkalifaDepartment of Immunology, Salford Royal National Health Service (NHS) Foundation Trust, Salford, United Kingdom.
Aarnoud HuissoonDepartment of Clinical Immunology, University Hospitals Birmingham National Health Service (NHS) Foundation Trust, Birmingham, United Kingdom.
Christopher J A DuncanDepartment of Infection and Tropical Medicine, Newcastle upon Tyne Hospitals National Health Service (NHS) Foundation Trust and Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.
Archana HerwadkarDepartment of Immunology, Salford Royal National Health Service (NHS) Foundation Trust, Salford, United Kingdom.
Sujoy KhanDepartment of Clinical Immunology, Hull University Teaching Hospitals National Health Service (NHS) Trust, Hull, United Kingdom.
Claire BethuneDepartment of Allergy and Clinical Immunology, University Hospitals Plymouth National Health Service (NHS) Trust, Plymouth, United Kingdom.
Suzanne ElcombeDepartment of Allergy and Clinical Immunology, Newcastle upon Tyne Hospitals National Health Service (NHS) Foundation Trust, Newcastle upon Tyne, Newcastle, United Kingdom.
James ThaventhiranMedical Research Council Toxicology Unit, University of Cambridge, Cambridge, United Kingdom.
Paul KlenermanNuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
David M LoweDepartment of Immunology, Royal Free London National Health Service (NHS) Foundation Trust, London, United Kingdom.
Sinisa SavicDepartment of Allergy and Clinical Immunology, Leeds Teaching Hospitals National Health Service (NHS) Trust, Leeds, United Kingdom.
Siobhan O BurnsDepartment of Immunology, Royal Free London National Health Service (NHS) Foundation Trust, London, United Kingdom.
Alex G RichterClinical Immunology Service, Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, United Kingdom.
National Health Service · GBNewcastle University · GBSalford Royal NHS Foundation Trust · GBUniversity College London · GBLeeds Teaching Hospitals NHS Trust · GBMedical Research Council · GBThe Royal Free Hospital · GBUniversity Hospitals Birmingham NHS Foundation Trust · GBUniversity Hospitals of North Midlands NHS Trust · GBUniversity of Oxford · GB

Funding

Medical Research Council MR/W002663/1Wellcome Trust 211153/Z/18/Z
6 · The paper itself

Abstract

Background: Individuals with primary and secondary immunodeficiency (PID/SID) were shown to be at risk of poor outcomes during the early stages of the SARS-CoV-2 pandemic. SARS-CoV-2 vaccines demonstrate reduced immunogenicity in these patients. Objectives: To understand whether the risk of severe COVID-19 in individuals with PID or SID has changed following the deployment of vaccination and therapeutics in the context of the emergence of novel viral variants of concern. Methods: The outcomes of two cohorts of patients with PID and SID were compared: the first, infected between March and July 2020, prior to vaccination and treatments, the second after these intervention became available between January 2021 and April 2022. Results: 22.7% of immunodeficient patients have been infected at least once with SARS-CoV-2 since the start of the pandemic, compared to over 70% of the general population. Immunodeficient patients were typically infected later in the pandemic when the B.1.1.529 (Omicron) variant was dominant. This delay was associated with receipt of more vaccine doses and higher pre-infection seroprevalence. Compared to March-July 2020, hospitalization rates (53.3% vs 17.9%, p<0.0001) and mortality (Infection fatality rate 20.0% vs 3.4%, p=0.0003) have significantly reduced for patients with PID but remain elevated compared to the general population. The presence of a serological response to vaccination was associated with a reduced duration of viral detection by PCR in the nasopharynx. Early outpatient treatment with antivirals or monoclonal antibodies reduced hospitalization during the Omicron wave. Conclusions: Most individuals with immunodeficiency in the United Kingdom remain SARS-CoV-2 infection naïve. Vaccination, widespread availability of outpatient treatments and, possibly, the emergence of the B.1.1.529 variant have led to significant improvements in morbidity and mortality followings SARS-CoV-2 infection since the start of the pandemic. However, individuals with PID and SID remain at significantly increased risk of poor outcomes compared to the general population; mitigation, vaccination and treatment strategies must be optimized to minimize the ongoing burden of the pandemic in these vulnerable cohorts.

Indexed as

COVID-19Antibodies, MonoclonalAntiviral AgentsCOVID-19 VaccinesHospitalizationHumansSARS-CoV-2Seroepidemiologic StudiesVaccinationAntibodies, MonoclonalAntiviral AgentsCOVID-19 VaccinesCOVID-19CVIDinborn errors of immunityprimary immunodeficiencySARS-CoV-2secondary immunodeficiencyvaccination

Identifiers

PMID36211396
PMCPMC9539662
OpenAlexW4296997848

What OpenQuestion holds

Textmetadata
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.