Evidence map›Paper›PMID 38042373›Full record

ArticleVirus research2024

IgM-specific linear epitopes on the E2 protein for serodiagnosis of Chikungunya.

Qianlin Li, Jun Dai, Yongxia Shi, Qiang Deng, Conghui Liao, Jicheng Huang, Jiahai Lu

Open access · goldAbstract read
In one paragraph

Article in Virus research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.6field-weighted citation impact, top 28% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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 2 institutions in 1 country.

Qianlin LiHealth Inspection and Quarantine Laboratory, Guangzhou Customs Technology Center, Guangzhou 510623, China; School of Public Health, Sun Yat-Sen University, Guangzhou 510080, China.
Jun DaiHealth Inspection and Quarantine Laboratory, Guangzhou Customs Technology Center, Guangzhou 510623, China.
Yongxia ShiHealth Inspection and Quarantine Laboratory, Guangzhou Customs Technology Center, Guangzhou 510623, China.
Qiang DengSchool of Public Health, Sun Yat-Sen University, Guangzhou 510080, China.
Conghui LiaoSchool of Public Health, Sun Yat-Sen University, Guangzhou 510080, China.
Jicheng HuangHealth Inspection and Quarantine Laboratory, Guangzhou Customs Technology Center, Guangzhou 510623, China. Electronic address: jichenghuang@126.com.
Jiahai LuInternational School of Public Health and One Health, Hainan Medical University, Hainan 571199, China; School of Public Health, Sun Yat-Sen University, Guangzhou 510080, China. Electronic address: lujiahai@mail.sysu.edu.cn.
Sun Yat-sen University · CNHainan Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chikungunya virus (CHIKV) and Dengue virus (DENV) are vector-borne diseases transmitted by Aedes aegypti and Aedes albopictus that pose a significant threat to global public health. Cases of acute Chikungunya fever often present similar clinical symptoms to other vector-borne diseases, such as Dengue fever. In regions where multiple vector-borne diseases coexist, CHIKV is often overlooked or misdiagnosed as Dengue virus, West Nile virus, Zika virus or other viral infections, which delays its prevention and control. However, IgM antibodies directed against the E2 protein of CHIKV have not yet been generalized to clinical settings due to the low sensitivity and high cost in commercial kits. Indirect ELISA with peptides provides an effective supplementary tool for detecting CHIKV IgM antibodies. Our study aims at examining the potential of linear epitopes on the E2 glycoprotein that specifically bind to IgM antibodies as serodiagnostic tool for CHIKV. The sensitivity of the established peptide indirect ELISA method for detecting clinical samples is significantly better than that of commercial kits, realizing a beneficial supplement to the existing IgM antibody assay. It also established the groundwork for comprehending the biological mechanisms of the CHIKV E2 protein and the advancement of innovative epitope peptide vaccines.

Indexed as

Chikungunya FeverChikungunya virusDengueZika VirusZika Virus InfectionAedesAntibodies, ViralEpitopesHumansImmunoglobulin MSerologic TestsViral ProteinsAntibodies, ViralEpitopesImmunoglobulin MViral ProteinsChikungunyaE2 proteinIgM antibodyPeptide microarray chipsSerodiagnosis

Identifiers

PMID38042373
PMCPMC10714233
OpenAlexW4389288791

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.