Evidence map›Paper›PMID 34703805›Full record

ArticleClinical and experimental vaccine research2021

Rania Ibrahim Shebl, Mohamed E Amer, Tamer M M Abuamara, Emadeldin R Matar, Hassan Fathy Ahmed, Tamer Albasyoni Gomah, Laila E El Moselhy, Mohammed Abu-Elghait, Aly Fahmy Mohamed

Open access · diamondAbstract read
In one paragraph

Article in Clinical and experimental vaccine research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
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  5. Review
  6. 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

9 authors at 2 institutions in 1 country.

Rania Ibrahim SheblMicrobiology and Immunology Department, Faculty of Pharmacy, Ahram Canadian University (ACU), Cairo, Egypt.ORCID https://orcid.org/0000-0003-2877-6196
Mohamed E AmerHistology Department, Faculty of Medicine, Al-Azhar University, Damietta, Egypt.ORCID https://orcid.org/0000-0001-5964-5362
Tamer M M AbuamaraHistology Department, Faculty of Medicine, Al-Azhar University, Cairo, Egypt.ORCID https://orcid.org/0000-0003-4326-3663
Emadeldin R MatarPathology Department, Faculty of Medicine, Al-Azhar University, Cairo, Egypt.ORCID https://orcid.org/0000-0003-2460-4100
Hassan Fathy AhmedHistology Department, Faculty of Medicine, Al-Azhar University, Cairo, Egypt.ORCID https://orcid.org/0000-0001-5385-0293
Tamer Albasyoni GomahHistology Department, Faculty of Medicine, Al-Azhar University, Damietta, Egypt.ORCID https://orcid.org/0000-0003-2370-3801
Laila E El MoselhyHistology Department, Faculty of Medicine, Al-Azhar University, Damietta, Egypt.ORCID https://orcid.org/0000-0002-1602-335X
Mohammed Abu-ElghaitBotany and Microbiology Department, Faculty of Science, Al-Azhar University, Cairo, Egypt.ORCID https://orcid.org/0000-0001-9007-1029
Aly Fahmy MohamedInternational Center for Training and Advanced Researches (ICTAR-Egypt), Cairo, Egypt.ORCID https://orcid.org/0000-0003-3629-3514
Al-Azhar University · EGAhram Canadian University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeOne of the essential goals regarding the successful control of rabies infection is the development of a safe, effective, and inexpensive vaccine. the current study aimed to evaluate the inactivation potential of β-propiolactone (βPL), binary ethyleneimine (BEI), and hydrogen peroxide (H MATERIALS AND

methodsEstimating the inactivation kinetics of βPL, BEI, and H

resultsResults demonstrated that both adjuvants could progressively enhance the release of anti-rabies total immunoglobulin G as well as the pro-inflammatory mediators (interferon-gamma and interleukin-5) relative to time. However, a higher immune response was developed in the case of HA adjuvanted rabies vaccine compared to PPD adjuvanted one. The harmful consequences of the tested adjuvants were considered via investigating the histopathological changes in the tissues of the immunized rats using hematoxylin and eosin stain. Lower adverse effects were observed post-vaccination with HA and PPD adjuvanted vaccines compared to that detected following administration of the currently used alum as standard adjuvant.

conclusionOur findings suggested that HA and PPD could serve as a promising platform for the development of newly adjuvanted rabies vaccines with elevated immune enhancing potentials and lower risk of health hazards.

Indexed as

Binary ethyleneimineHyaluronic acidImmune enhancersRabies vaccinesβ-Propiolactone

Identifiers

PMID34703805
PMCPMC8511591
OpenAlexW3206993334

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.