Evidence map›Paper›PMID 37464326›Full record

ArticleBMC infectious diseases2023

Neutralizing activity of intravenous immune globulin products against enterovirus D68 strains isolated in Japan.

Kazuhiro Yoshida, Masamichi Muramatsu, Hiroyuki Shimizu

Open access · goldAbstract read
In one paragraph

Article in BMC infectious diseases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 34% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

3 authors at 1 institution in 1 country.

Kazuhiro YoshidaDepartment of Virology 2, National Institute of Infectious Diseases, Tokyo, Japan. 6yoshida12@gmail.com.
Masamichi MuramatsuDepartment of Virology 2, National Institute of Infectious Diseases, Tokyo, Japan.
Hiroyuki ShimizuDepartment of Virology 2, National Institute of Infectious Diseases, Tokyo, Japan.
National Institute of Infectious Diseases · JP

Funding

the Japan Agency for Medical Research and Development 19fk0108084j0001the Ministry of Education, Culture, Sports, Science, and Technology in Japan 19H03626the Ministry of Health, Labour and Welfare of Japan H28-Shinkogyosei-Ippan-007
6 · The paper itself

Abstract

backgroundEnterovirus D68 (EV-D68), belonging to Enterovirus D, is a unique human enterovirus mainly associated with common respiratory diseases. However, EV-D68 can cause severe respiratory diseases, and EV-D68 endemic is epidemiologically linked to current global epidemic of acute flaccid myelitis.

methodsIn this study, we measured neutralizing antibody titers against six clinical EV-D68 isolates in nine intravenous immune globulin (IVIG) products commercially available in Japan to assess their potential as therapeutic options for severe EV-D68 infection.

resultsSeven IVIG products manufactured from Japanese donors contained high neutralizing antibody titers (IC

conclusionsHigh levels of EV-D68-neutralizing antibodies in IVIG products manufactured from Japanese donors suggest that anti-EV-D68 antibodies are maintained in the Japanese donor population similarly as found in foreign blood donors. Apparent differences in neutralizing antibody titers against the six EV-D68 strains suggest distinct antigenicity among the strains used in this study regardless of the genetic similarity of EV-D68.

Indexed as

EnterovirusEnterovirus D, HumanEnterovirus InfectionsAntibodies, NeutralizingHumansImmunoglobulins, IntravenousJapanAntibodies, NeutralizingImmunoglobulins, IntravenousEnterovirus D68IVIGJapanNeutralization activity

Identifiers

PMID37464326
PMCPMC10394975
OpenAlexW4384665348

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LicenceCC BY
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Registered trials

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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.