Evidence map›Paper›PMID 24178189›Full record

ReviewInfection2014

Development of universal influenza vaccines based on influenza virus M and NP genes.

M Zheng, J Luo, Z Chen

Abstract readReview
PubMed Publisher
In one paragraph

Review in Infection, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

47 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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.

M ZhengShanghai Institute of Biological Products, Shanghai, 200052, China.
J Luo
Z Chen

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeVaccination is the safest and most effective measure against influenza virus infections. However, traditional influenza vaccines cannot respond effectively to an unforeseen epidemic or pandemic caused by a virus with antigenic drifts or antigenic shifts. Therefore, developing a universal influenza vaccine (UIV) that induces broad-spectrum and long-term immunity has become a major trend in influenza vaccine research and development.

methodsThis article reviews the development of UIVs based on these conserved influenza virus proteins. RESULTS AND

conclusionThe matrix protein (M1, M2) and nucleoprotein (NP) of influenza viruses have highly conserved sequences, and they become the major target antigens of current UIV studies.

Indexed as

AnimalsChickensHumansInfluenza, HumanInfluenza in BirdsInfluenza VaccinesMiceNucleocapsid ProteinsOrthomyxoviridaeOrthomyxoviridae InfectionsRNA-Binding ProteinsViral Core ProteinsViral Matrix ProteinsViroporin ProteinsInfluenza VaccinesM1 protein, Influenza A virusM2 protein, Influenza A virusNP protein, Influenza A virusNucleocapsid ProteinsRNA-Binding ProteinsViral Core ProteinsViral Matrix ProteinsViroporin Proteins

Identifiers

What OpenQuestion holds

Textmetadata
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.