Evidence map›Paper›PMID 32089462›Full record

ArticleVaccine2020

Neutralization capacity of highly divergent type 2 vaccine-derived polioviruses from immunodeficient patients.

Sharla L McDonald, William C Weldon, Ling Wei, Qi Chen, Jing Shaw, Kun Zhao, Jaume Jorba, Olen M Kew, Mark A Pallansch, Cara C Burns and 1 more

Open access · greenAbstract read
In one paragraph

Article in Vaccine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

5 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Monogenic susceptibility to live viral vaccines.Current opinion in immunology · 2021
    Review
  5. 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

11 authors at 1 institution in 1 country.

Sharla L McDonaldIHRC, Inc. Atlanta, GA, Under Contract with Polio and Picornavirus Laboratory Branch, Centers for Disease Control and Prevention, USA.
William C WeldonDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Ling WeiIHRC, Inc. Atlanta, GA, Under Contract with Polio and Picornavirus Laboratory Branch, Centers for Disease Control and Prevention, USA.
Qi ChenDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Jing ShawDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Kun ZhaoDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Jaume JorbaDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Olen M KewDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Mark A PallanschDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
Cara C BurnsDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA.
M Steven ObersteDivision of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA. Electronic address: mbo2@cdc.gov.
Centers for Disease Control and Prevention · US

Funding

Intramural CDC HHS CC999999
6 · The paper itself

Abstract

The use of the oral poliovirus vaccine (OPV) in developing countries has reduced the incidence of poliomyelitis by >99% since 1988 and is the primary tool for global polio eradication. Spontaneous reversions of the vaccine virus to a neurovirulent form can impede this effort. In persons with primary B-cell immunodeficiencies, exposure to OPV can result in chronic infection, mutation, and excretion of immunodeficiency-associated vaccine-derived polioviruses, (iVDPVs). These iVDPVs may have the potential for transmission in a susceptible population and cause paralysis. The extent to which sera from OPV recipients are able to neutralize iVDPVs with varying degrees of antigenic site substitutions is investigated here. We tested sera from a population immunized with a combination vaccine schedule (both OPV and inactivated polio vaccine) against a panel of iVDPVs and found that increases in amino acid substitution in the P1 capsid protein resulted in a decrease in the neutralizing capacity of the sera. This study underscores the importance of maintaining high vaccine coverage in areas of OPV use as well as active surveillance of those known to be immunocompromised.

Indexed as

Immunologic Deficiency SyndromesPoliomyelitisPoliovirusPoliovirus Vaccine, OralAmino Acid SubstitutionAntibodies, NeoplasmAntibodies, ViralCapsid ProteinsGlobal HealthHumansPoliovirus Vaccine, InactivatedAntibodies, NeoplasmAntibodies, ViralCapsid ProteinsPoliovirus Vaccine, InactivatedPoliovirus Vaccine, OraliVDPVNeutralizationPolioVaccine-derived

Identifiers

PMID32089462
PMCPMC11382130
OpenAlexW3006931331

What OpenQuestion holds

Textmetadata
LicenceTDM
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.