Evidence map›Paper›PMID 27019828›Full record

ArticleGerms2016

IL-17 and IL-22 genetic polymorphisms in HBV vaccine non- and low-responders among healthcare workers.

Zohreh Borzooy, Adrian Streinu-Cercel, Abbass Mirshafiey, Azam Khamseh, Masoud Karkhaneh Mahmoudie, Shadi Sadat Navabi, Marjan Nosrati, Zahra Najafi, Mostafa Hosseini, Seyed Mohammad Jazayeri

Abstract read
In one paragraph

Article in Germs, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

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  5. Vaccinomics and adversomics: key elements for a personalized vaccinology.Clinical and experimental vaccine research · 2024
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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

10 authors at 3 institutions in 4 countries.

Zohreh BorzooyPhD student, Department of Infectious Diseases, Faculty of Medicine, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania; Department of Immunology and Department of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Adrian Streinu-CercelMD, PhD, Department of Infectious Diseases, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania; National Institute of Infectious Diseases, "Prof. Dr. Matei Balş", Bucharest, Romania.
Abbass MirshafieyMs, PhD, Head of the department of Pathobiology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Azam KhamsehBs, Department of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Masoud Karkhaneh MahmoudieBs, Department of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Shadi Sadat NavabiMs, Department of Immunology, Tehran University of Medical Sciences, Tehran, Iran.
Marjan NosratiBs, Department of Infection Control, Tehran Heart Center, Tehran University of Medical Sciences, Tehran, Iran.
Zahra NajafiMs, Bahrami Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Mostafa HosseiniMs, PhD, Department of Epidemiology and Biostatistics School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Seyed Mohammad JazayeriMD, PhD, Clinical Virologist, Hepatitis B Molecular Laboratory, Department of Virology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Tehran University of Medical Sciences · IRNational Institute of Research and Development for Biological Sciences · ROOffice of Infectious Diseases · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHealthcare workers constitute a population at high risk for HBV infection. Efficient vaccination options are available; however, the individual response to HBV vaccination may vary widely between subjects, potentially due to cytokine profiles and genetic variations. In the present study, we investigated the relationship between IL-17 and IL-22 gene polymorphisms versus non- and low-responsiveness to HBV vaccination in healthcare workers.

methodsWe selected the following IL-17 and IL-22 polymorphisms: rs4711998 (A/G) from IL-17 and rs2227501 (A/T), rs2227503 (A/G), rs1026786 (A/G) from IL-22 sequences genes. These were determined by polymerase chain reaction restriction fragment length polymorphisms.

resultsThe IL-17 rs4711998 GG genotype had a significantly lower frequency in non-responders compared to low-responders (p=0.025). However, we did not identify a relationship between IL-22 rs1026780, rs2227501 and rs2227503 genotypes and the anti-HBs response following HBV vaccination.

conclusionThese data suggest that genetic variation in rs4711998 polymorphisms in the IL-17 cytokine may influence vaccine-induced immune responses to HBV vaccine in healthcare workers.

Indexed as

gene polymorphismsHBV vaccinehealthcare workersIL-17IL-22

Identifiers

PMID27019828
PMCPMC4788777
OpenAlexW2416526489

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.