Evidence map›Paper›PMID 16412060›Full record

ArticleClinical and experimental immunology2006

NK cells, displaying early activation, cytotoxicity and adhesion molecules, are associated with mild dengue disease.

E L Azeredo, L M De Oliveira-Pinto, S M Zagne, D I S Cerqueira, R M R Nogueira, C F Kubelka

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Clinical and experimental immunology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05611710 (Anakinra for Dengue Patients With Hyperinflammation - a Randomized Double-blind Placebo-controlled Trial), which is not on this map. Cited by 73 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed, 2 pooled it
0.9field-weighted citation impact, top 27% 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.

NCT05611710 phase2active not recruitingnot on this mapstarted 2023, after this paper: background citation

Anakinra for Dengue Patients With Hyperinflammation - a Randomized Double-blind Placebo-controlled Trial

TypeinterventionalSponsorOxford University Clinical Research Unit, VietnamRan2023 to 2027Enrolled160ConditionsDengue, Dengue With Warning Signs, Severe Dengue, AnakinraArmsPlacebo, Anakinra
3 · Its place in the literature

Who cites it

73 citing papers in PubMed, 2 syntheses or guidelines pooled it, 137 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Article
  6. Innate Immune and Inflammatory Responses to Dengue Virus Infection.Current topics in microbiology and immunology · 2026
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Observational
  16. Review
  17. Review
  18. Article
  19. IL-15 induced bystander activation of CD8Frontiers in cellular and infection microbiology · 2022
    Article
  20. Host immune response against DENV and ZIKV infections.Frontiers in cellular and infection microbiology · 2022
    Review

13 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 1 country.

E L AzeredoDepartment of Virology, Oswaldo Cruz Institute, Fiocruz, Rio de Janeiro, Brazil.
L M De Oliveira-Pinto
S M Zagne
D I S Cerqueira
R M R Nogueira
C F Kubelka
Fundação Oswaldo Cruz · BRHospital Universitário Antônio Pedro · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During the innate immune response against infections, Natural Killer (NK) cells are as important effector cells as are Cytotoxic T lymphocytes (CTL) generated after antigenic stimulation in the adaptative response. NK cells increase in numbers, after viral infection or vaccination. We investigated the NK cell and CD8 T lymphocyte status in 55 dengue infected patients. The NK (CD56+CD3-) and CD56+ T cell (CD56+CD3+) rates rise during the acute phase of disease. The majority of NK cells from dengue patients display early markers for activation (CD69, HLA-DR, and CD38) and cell adhesion molecules (CD44, CD11a) during the acute phase of disease. The intracellular cytotoxic granule, TIA-1, is also up-regulated early in NK cells. Most of these markers appear also on CD8+ T lymphocytes but during the late acute phase. Circulating IL-15 is elevated in a significant number of patients during early acute infection and its values were statistically correlated with NK frequencies and cytotoxic markers on NKs. We have therefore shown that dengue virus infection is very likely stimulating a cytotoxic response that may be efficient in controlling the virus in synergism with CD8+ T lymphocytes. Interestingly, the heightened CD56+CD3-, CD56+CD3+, CD56+TIA-1+ and CD56+CD11a+ cell rates are associated with mild dengue clinical manifestations and might indicate a good prognosis of the disease.

Indexed as

AdolescentAdultAntigens, CDAntigens, Differentiation, T-LymphocyteBiomarkersCD11a AntigenCD3 ComplexCD56 AntigenCD69 AntigensCD8-Positive T-LymphocytesCell Adhesion MoleculesCytotoxicity, ImmunologicDengueFemaleHumansHyaluronan ReceptorsAntigens, CDAntigens, Differentiation, T-LymphocyteBiomarkersCD11a AntigenCD3 ComplexCD56 AntigenCD69 AntigensCell Adhesion MoleculesHyaluronan ReceptorsInterleukin-15Lectins, C-TypeReceptors, IgGRNA-Binding ProteinsTIAL1 protein, human

Identifiers

PMID16412060
PMCPMC1809585
OpenAlexW2051335877

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.