Evidence map›Paper›PMID 32292408›Full record

ArticleFrontiers in immunology2020

Hepatitis B Core Antigen Impairs the Polarization While Promoting the Production of Inflammatory Cytokines of M2 Macrophages via the TLR2 Pathway.

Hongyu Yi, Ye Zhang, Xiaofei Yang, Mengyuan Li, Haifeng Hu, Jie Xiong, Ning Wang, Jingyi Jin, Yusi Zhang, Yun Song and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

28 citing papers in PubMed, 37 citations in OpenAlex.

  1. Liver Macrophages in the Pathogenesis of Viral Hepatitis.Current issues in molecular biology · 2026
    Review
  2. Review
  3. New Insights into the Role of NF-κB in Hepatitis B Virus Infection.International journal of biological sciences · 2026
    Review
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  16. Inflammation and tumor microenvironment.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2023
    Review
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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

13 authors at 1 institution in 1 country.

Hongyu YiDepartment of Infectious Diseases, Tangdu Hospital, The Fourth Military Medical University, Xi'an, China.
Ye ZhangDepartment of Infectious Diseases, Tangdu Hospital, The Fourth Military Medical University, Xi'an, China.
Xiaofei YangDepartment of Infectious Diseases, Tangdu Hospital, The Fourth Military Medical University, Xi'an, China.
Mengyuan LiDepartment of Infectious Diseases, Tangdu Hospital, The Fourth Military Medical University, Xi'an, China.
Haifeng HuDepartment of Infectious Diseases, Tangdu Hospital, The Fourth Military Medical University, Xi'an, China.
Jie XiongDepartment of Respiratory and Critical Care, Xijing Hospital, The Fourth Military Medical University, Xi'an, China.
Ning WangDepartment of Immunology, The Fourth Military Medical University, Xi'an, China.
Jingyi JinDepartment of Immunology, The Fourth Military Medical University, Xi'an, China.
Yusi ZhangDepartment of Immunology, The Fourth Military Medical University, Xi'an, China.
Yun SongDepartment of Immunology, The Fourth Military Medical University, Xi'an, China.
Xian WangDepartment of Immunology, The Fourth Military Medical University, Xi'an, China.
Lihua ChenDepartment of Immunology, The Fourth Military Medical University, Xi'an, China.
Jianqi LianDepartment of Infectious Diseases, Tangdu Hospital, The Fourth Military Medical University, Xi'an, China.
Air Force Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although several evidences suggesting the vital roles that innate immunity plays in the persistence and elimination of chronic hepatitis B virus (CHB) infection, the exact mechanism is still complicated. Here, we successfully polarized monocytes derived from healthy human peripheral blood mononuclear cells (PBMCs) into M1/M2 macrophages and detected the effects of hepatitis B core antigen (HBcAg) on the polarization and function of macrophages via the Toll-like receptor (TLR) 2 signaling pathway. The results showed that HBcAg had a negligible impact on M1 polarization, while it effectively impaired M2 polarization and promoted the production of pro-inflammatory cytokines such as IL-6 and TNF-α. Additionally, HBcAg treatment increased TLR2 expression on M2 macrophages and TLR2 blockade abolished the effects of HBcAg on the impaired phenotype and pro-inflammatory cytokine productions of M2 macrophages. Signaling pathway analysis revealed that the nuclear factor κB (NF-κB) pathway, the downstream of TLR2, was upregulated upon HBcAg treatment in both M1 and M2 macrophages. Furthermore, a CD8

Indexed as

CD8-Positive T-LymphocytesCell Culture TechniquesCell DifferentiationCoculture TechniquesCytokinesHepatitis B, ChronicHepatitis B Core AntigensHumansImmunity, InnateInflammationLymphocyte ActivationMacrophage ActivationMacrophagesSignal TransductionToll-Like Receptor 2CytokinesHepatitis B Core AntigensTLR2 protein, humanToll-Like Receptor 2HBV core proteinhepatitis B virusinflammatory cytokinesmacrophage polarizationToll-like receptor 2

Identifiers

PMID32292408
PMCPMC7118225
OpenAlexW3013980941

What OpenQuestion holds

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LicenceCC BY
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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.