Evidence map›Paper›PMID 31913852›Full record

ArticleJournal of integrative bioinformatics2020

Predicting and Designing Epitope Ensemble Vaccines against HTLV-1.

Saruar Alam, Md Kamrul Hasan, Omar Hamza Bin Manjur, Akib Mahmud Khan, Zinat Sharmin, Mahmud Arif Pavel, Md Faruk Hossain

Open access · diamondAbstract read
In one paragraph

Article in Journal of integrative bioinformatics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
0.7field-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

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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it, 19 citations in OpenAlex.

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  11. Vaccines for immunoprevention of cancer.The Journal of clinical investigation · 2021
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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

7 authors at 4 institutions in 2 countries.

Saruar AlamDepartment of Biochemistry and Molecular Biology, University of Dhaka, Dhaka, Bangladesh.
Md Kamrul HasanDepartment of Biochemistry and Molecular Biology, University of Dhaka, Dhaka, Bangladesh.
Omar Hamza Bin ManjurDepartment of Biochemistry and Molecular Biology, University of Dhaka, Dhaka, Bangladesh.
Akib Mahmud KhanDepartment of Biochemistry and Molecular Biology, University of Dhaka, Dhaka, Bangladesh.
Zinat SharminDepartment of Biology, Florida International University, Miami, FL, USA.
Mahmud Arif PavelDepartment of Neuroscience, The Scripps Research Institute, Jupiter, FL, USA.
Md Faruk HossainSt. John's University, Department of Biological Sciences, Queens, NY 11439, USA.ORCID https://orcid.org/0000-0002-3457-7903
University of Dhaka · BDFlorida International University · USScripps Research Institute · USSt. John's University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The infection mechanism and pathogenicity of Human T-lymphotropic virus 1 (HTLV-1) are ambiguously known for hundreds of years. Our knowledge about this virus is recently emerging. The purpose of the study is to design a vaccine targeting the envelope glycoprotein, GP62, an outer membrane protein of HTLV-1 that has an increased number of epitope binding sites. Data collection, clustering and multiple sequence alignment of HTLV-1 glycoprotein B, variability analysis of envelope Glycoprotein GP62 of HTLV-1, population protection coverage, HLA-epitope binding prediction, and B-cell epitope prediction were performed to predict an effective vaccine. Among all the predicted peptides, ALQTGITLV and VPSSSTPL epitopes interact with three MHC alleles. The summative population protection coverage worldwide by these epitopes as vaccine candidates was found nearly 70%. The docking analysis revealed that ALQTGITLV and VPSSSTPL epitopes interact strongly with the epitope-binding groove of HLA-A*02:03, and HLA-B*35:01, respectively, as this HLA molecule was found common with which every predicted epitope interacts. Molecular dynamics simulations of the docked complexes show they form stable complexes. So, these potential epitopes might pave the way for vaccine development against HTLV-1.

Indexed as

AllelesAmino Acid SequenceComputational BiologyEpitopes, B-LymphocyteHLA AntigensHumansHuman T-lymphotropic virus 1Major Histocompatibility ComplexMolecular Dynamics SimulationPeptidesProtein BindingViral VaccinesEpitopes, B-LymphocyteHLA AntigensPeptidesViral Vaccinesenvelope glycoprotein GP62HTLV-1Human T-lymphotropic virus 1Vaccine design

Identifiers

PMID31913852
PMCPMC7074140
OpenAlexW3000079346

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.