Evidence map›Paper›PMID 32671251›Full record

ArticleHeliyon2020

Impaired NK cell activation during acute dengue virus infection: A contributing factor to disease severity.

Snehal Shabrish, Niteen Karnik, Vishal Gupta, Priya Bhate, Manisha Madkaikar

Open access · goldAbstract read
In one paragraph

Article in Heliyon, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.2field-weighted citation impact, top 52% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
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

5 authors at 2 institutions in 1 country.

Snehal ShabrishDepartment of Paediatric Immunology and Leukocyte Biology, ICMR-National Institute of Immunohaematology (NIIH), 13th floor, Multistoreyed building, KEM Hospital Campus, Parel, Mumbai 400 012, India.
Niteen KarnikDepartment of Medicine, KEM Hospital, Parel, Mumbai 400 012, India.
Vishal GuptaDepartment of Medicine, KEM Hospital, Parel, Mumbai 400 012, India.
Priya BhateDepartment of Medicine, KEM Hospital, Parel, Mumbai 400 012, India.
Manisha MadkaikarDepartment of Paediatric Immunology and Leukocyte Biology, ICMR-National Institute of Immunohaematology (NIIH), 13th floor, Multistoreyed building, KEM Hospital Campus, Parel, Mumbai 400 012, India.
College of Medicine & JNM Hospital · INNational Institute of Immunohaematology · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dengue viral (DENV) infection has a broad clinical spectrum ranging from classical febrile illness to life-threatening disease. Literature suggests that spectrum of illness could be due to differences in innate immune-responses; however, the knowledge is still at infancy. Amongst the various cells involved in innate immune responses, NK cells play a central role, particularly in anti-viral immunity. Thus in this study we have evaluated the role of NK-cells during acute-DENV infection and its influence on severity of disease, by analyzing activation, cytotoxic receptors, cytolytic granule contents and degranulation markers on NK-cells during different stages of infection. Based on the clinical manifestations and severity of the disease, DENV patients were classified into patients with dengue without warning signs (DF), dengue with warning signs (DFWS) and severe dengue (SD) patients. During acute-DENV infection, though there was no alteration in frequency of NK-cells, significant increase in frequency of CD56

Indexed as

Hematological systemImmunologyImmunopathogenesisInfectious diseaseMicrobiologyNK cell responsePublic healthSevere dengue viral infectionVirology

Identifiers

PMID32671251
PMCPMC7339061
OpenAlexW3040593132

What OpenQuestion holds

Textmetadata
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.