Evidence map›Paper›PMID 8972566›Full record

ArticleVirus genes1996

Prediction of potential cytotoxic T lymphocyte epitopes of bovine herpesvirus 1 based on allele-specific peptide motifs and proteolytic cleavage specificities.

N R Hegde, S Srikumaran

Abstract read
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In one paragraph

Article in Virus genes, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
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

2 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
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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

2 authors at 1 institution in 1 country.

N R HegdeDepartment of Veterinary and Biomedical Sciences, University of Nebraska-Lincoln 68583-0905, USA. nhegde@crcvms.unl.edu
S Srikumaran
University of Nebraska–Lincoln · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Major histocompatibility complex (MHC) class I molecules present endogenous peptides to cytotoxic T lymphocytes (CTLs). Elucidation of CTL epitopes of intracellular pathogens helps in designing better vaccines to control economically important human and animal diseases. In this study, candidate epitopes that are potentially available for presentation to the CTLs via five bovine MHC class I molecules have been identified. This was accomplished by using the computer programs "Find-patterns" and "Peptidestructure" of GCG package and applying the information on cleavage patterns of cytosolic and endoplasmic reticulum proteases and peptidases as well as MHC class I allele-specific peptide motifs on 23 bovine herpesvirus-1 (BHV-1) proteins available on protein sequence database. Several candidate peptides were found for each of the bovine lymphocyte antigens (BoLA)-A11, -A20, -HD1, and -HD6 whereas no peptide was found for BoLA-HD7. Majority of the candidate peptides were from the viral glycoproteins. The contribution of such studies towards the identification of CTL epitopes of BHV-1 and other intracellular pathogens is discussed.

Indexed as

Epitope MappingAllelesAmino Acid SequenceAnimalsAntigens, ViralCattleEndopeptidasesEpitopes, T-LymphocyteGene FrequencyHerpesvirus 1, BovineHistocompatibility Antigens Class IMolecular Sequence DataPeptidesT-Lymphocytes, CytotoxicAntigens, ViralEndopeptidasesEpitopes, T-LymphocyteHistocompatibility Antigens Class IPeptides

Identifiers

PMID8972566
OpenAlexW2081958211

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.