Evidence map›Paper›PMID 37696512›Full record

ArticleThe American journal of tropical medicine and hygiene2023

Clinical, Virological, and Immunological Features in Cosmopolitan Genotype DENV-2-Infected Patients during a Large Dengue Outbreak in Sri Lanka in 2017.

Khine Mya Nwe, Mya Myat Ngwe Tun, Rohitha Muthugala, Takeshi Nabeshima, Jean Claude Balingit, Lakmali Rajamanthri, Dulani Jayawardana, Shanthi Attanayake, Shingo Inoue, Yuki Takamatsu and 2 more

Open access · greenAbstract read
In one paragraph

Article in The American journal of tropical medicine and hygiene, 2023. 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
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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
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

12 authors at 3 institutions in 2 countries.

Khine Mya NweDepartment of Virology, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.
Mya Myat Ngwe TunDepartment of Virology, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.
Rohitha MuthugalaDepartment of Virology, National Hospital Kandy, Kandy, Sri Lanka.
Takeshi NabeshimaKenya Research Station, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.
Jean Claude BalingitDepartment of Virology, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.
Lakmali RajamanthriDepartment of Virology, National Hospital Kandy, Kandy, Sri Lanka.
Dulani JayawardanaDepartment of Virology, National Hospital Kandy, Kandy, Sri Lanka.
Shanthi AttanayakeDepartment of Virology, National Hospital Kandy, Kandy, Sri Lanka.
Shingo InoueKenya Research Station, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.
Yuki TakamatsuDepartment of Virology, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.
Takeshi UranoCenter for Vaccines and Therapeutic Antibodies for Emerging Infectious Diseases, Shimane University, Izumo, Japan.
Kouichi MoritaDepartment of Virology, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.
Nagasaki University · JPTeaching Hospital Kandy · LKShimane University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In 2017, Sri Lanka experienced its largest dengue epidemic and reported severe and unusual presentations of dengue with high morbidity. This outbreak was associated with the reemergence of dengue virus-2 (DENV-2), with the responsible strain identified as a variant of the previously circulating DENV-2 cosmopolitan genotype. In this study, we characterized the DENV-2 cosmopolitan genotype from patients during this epidemic. Also, we identified host factors that contributed to the severity of dengue infection in patients infected with this particular virus. Ninety-one acute serum samples from patients at the National Hospital in Kandy were randomly selected. Of these, 40.2% and 48.9% were positive for dengue IgM and IgG, respectively. NS1 antigen levels were significantly higher in primary infections. The severe dengue (SD) and dengue with warning signs (DWWS) groups exhibited significantly higher viral genome and infectivity titers than the dengue without warning signs (DWoWS) group. The highest viremia level was observed in SD patients. As for host cytokine response, interferon α (IFN-α) levels were significantly higher in the DWoWS group than in the DWWS and SD groups, whereas interleukin (IL)-12p40 and tumor necrosis factor α (TNF-α) levels in SD patients were significantly higher than in the other two groups. The TNF-α, IL-4, and monocyte chemoattractant protein-1 concentrations were positively correlated with NS1 antigen levels. From whole-genome analysis, NS4 had the highest frequency of amino acid variants, followed by the E gene. Our study suggests that viremia levels and immune responses contributed to SD outcomes, and these findings may help in identifying an effective therapeutic strategy against SD infection.

Indexed as

DengueDengue VirusSevere DengueAntibodies, ViralDisease OutbreaksGenotypeHumansImmunoglobulin MSri LankaTumor Necrosis Factor-alphaViremiaAntibodies, ViralImmunoglobulin MTumor Necrosis Factor-alpha

Identifiers

PMID37696512
PMCPMC10551097
OpenAlexW4386608353

What OpenQuestion holds

Textmetadata
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.