Evidence map›Paper›PMID 37112692›Full record

ArticleVaccines2023

Intradermal Immunization of Soluble Influenza HA Derived from a Lethal Virus Induces High Magnitude and Breadth of Antibody Responses and Provides Complete Protection In Vivo.

Sneha Raj, Preeti Vishwakarma, Shikha Saxena, Varun Kumar, Ritika Khatri, Amit Kumar, Mrityunjay Singh, Surbhi Mishra, Shailendra Asthana, Shubbir Ahmed and 1 more

Open access · goldAbstract read
In one paragraph

Article in Vaccines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 20% 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, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
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.

Sneha RajTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad 121001, India.
Preeti VishwakarmaTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad 121001, India.ORCID 0000-0001-8530-4860
Shikha SaxenaTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad 121001, India.
Varun KumarTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad 121001, India.
Ritika KhatriTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad 121001, India.
Amit KumarTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad 121001, India.
Mrityunjay SinghTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad 121001, India.
Surbhi MishraTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad 121001, India.
Shailendra AsthanaTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad 121001, India.
Shubbir AhmedCentralized Core Research Facility (CCRF), All India Institute of Medical Sciences, New Delhi 110029, India.
Sweety SamalTranslational Health Science & Technology Institute, NCR Biotech Science Cluster, Faridabad 121001, India.
Translational Health Science and Technology Institute · IN

Funding

Department of Biotechnology BT/PR5480/INF/22/158/2012
6 · The paper itself

Abstract

Immunogens mimicking the native-like structure of surface-exposed viral antigens are considered promising vaccine candidates. Influenza viruses are important zoonotic respiratory viruses with high pandemic potential. Recombinant soluble hemagglutinin (HA) glycoprotein-based protein subunit vaccines against Influenza have been shown to induce protective efficacy when administered intramuscularly. Here, we have expressed a recombinant soluble trimeric HA protein in Expi 293F cells and purified the protein derived from the Inf A/Guangdong-Maonan/ SWL1536/2019 virus which was found to be highly virulent in the mouse. The trimeric HA protein was found to be in the oligomeric state, highly stable, and the efficacy study in the BALB/c mouse challenge model through intradermal immunization with the prime-boost regimen conferred complete protection against a high lethal dose of homologous and mouse-adapted InfA/PR8 virus challenge. Furthermore, the immunogen induced high hemagglutinin inhibition (HI) titers and showed cross-protection against other Inf A and Inf B subtypes. The results are promising and warrant trimeric HA as a suitable vaccine candidate.

Indexed as

hemagglutinininfluenzaintradermal routevaccinevirus

Identifiers

PMID37112692
PMCPMC10141624
OpenAlexW4362583145

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.