Evidence map›Paper›PMID 37498378›Full record

ArticleApplied biochemistry and biotechnology2024

An Immunoinformatics-Based Study of Mycobacterium tuberculosis Region of Difference-2 Uncharacterized Protein (Rv1987) as a Potential Subunit Vaccine Candidate for Preliminary Ex Vivo Analysis.

Aregitu Mekuriaw Arega, Ajit Kumar Dhal, Kali Prasad Pattanaik, Sasmita Nayak, Rajani Kanta Mahapatra

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Article in Applied biochemistry and biotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

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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

3 citing papers in PubMed, 4 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

Aregitu Mekuriaw AregaSchool of Biotechnology, KIIT Deemed to Be University, Bhubaneswar, Odisha, India.
Ajit Kumar DhalSchool of Biotechnology, KIIT Deemed to Be University, Bhubaneswar, Odisha, India.
Kali Prasad PattanaikSchool of Biotechnology, KIIT Deemed to Be University, Bhubaneswar, Odisha, India.
Sasmita NayakSchool of Biotechnology, KIIT Deemed to Be University, Bhubaneswar, Odisha, India.
Rajani Kanta MahapatraSchool of Biotechnology, KIIT Deemed to Be University, Bhubaneswar, Odisha, India. rmahapatra@kiitbiotech.ac.in.ORCID http://orcid.org/0000-0002-3654-2421
KIIT University · INNational Veterinary Institute · ET

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mycobacterium tuberculosis (Mtb) is the pathogen that causes tuberculosis and develops resistance to many of the existing drugs. The sole licensed TB vaccine, BCG, is unable to provide a comprehensive defense. So, it is crucial to maintain the immunological response to eliminate tuberculosis. Our previous in silico study reported five uncharacterized proteins as potential vaccine antigens. In this article, we considered the uncharacterized Mtb H37Rv regions of difference (RD-2) Rv1987 protein as a promising vaccine candidate. The vaccine quality of the protein was analyzed using reverse vaccinology and immunoinformatics-based quality-checking parameters followed by an ex vivo preliminary investigation. In silico analysis of Rv1987 protein predicted it as surface localized, secretory, single helix, antigenic, non-allergenic, and non-homologous to the host protein. Immunoinformatics analysis of Rv1987 by CD4 + and CD8 + T-cells via MHC-I and MHC-II binding affinity and presence of B-cell epitope predicted its immunogenicity. The docked complex analysis of the 3D model structure of the protein with immune cell receptor TLR-4 revealed the protein's capability for potential interaction. Furthermore, the target protein-encoded gene Rv1987 was cloned, over-expressed, purified, and analyzed by mass spectrometry (MS) to report the target peptides. The qRT-PCR gene expression analysis shows that it is capable of activating macrophages and significantly increasing the production of a number of key cytokines (TNF-α, IL-1β, and IL-10). Our in-silico analysis and ex vivo preliminary investigations revealed the immunogenic potential of the target protein. These findings suggest that the Rv1987 be undertaken as a potent subunit vaccine antigen and that further animal model immuno-modulation studies would boost the novel TB vaccine discovery and/or BCG vaccine supplement pipeline.

Indexed as

Bacterial ProteinsMycobacterium tuberculosisTuberculosis VaccinesVaccines, SubunitAnimalsAntigens, BacterialCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesComputational BiologyEpitopes, B-LymphocyteHumansImmunoinformaticsMiceMolecular Docking SimulationToll-Like Receptor 4TuberculosisAntigens, BacterialBacterial ProteinsEpitopes, B-LymphocyteToll-Like Receptor 4Tuberculosis VaccinesVaccines, SubunitCloneEx vivoIn silicoMolecular dynamics simulationMtbRv1987qRT-PCRVaccine

Identifiers

PMID37498378
OpenAlexW4385295256

What OpenQuestion holds

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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.