Evidence map›Paper›PMID 24945350›Full record

ArticlePLoS neglected tropical diseases2014

Invariant NKT cell response to dengue virus infection in human.

Ponpan Matangkasombut, Wilawan Chan-In, Anunya Opasawaschai, Pisut Pongchaikul, Nattaya Tangthawornchaikul, Sirijitt Vasanawathana, Wannee Limpitikul, Prida Malasit, Thaneeya Duangchinda, Gavin Screaton and 1 more

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.9field-weighted citation impact, top 7% 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

20 citing papers in PubMed, 29 citations in OpenAlex.

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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

11 authors at 5 institutions in 2 countries.

Ponpan MatangkasombutDepartment of Microbiology, Faculty of Science, Mahidol University, Bangkok, Thailand; Systems Biology of Diseases Research Unit, Faculty of Science, Mahidol University, Bangkok, Thailand; Center of Emerging and Neglected Infectious Diseases, Mahidol University, Bangkok, Thailand.
Wilawan Chan-InDepartment of Microbiology, Faculty of Science, Mahidol University, Bangkok, Thailand.
Anunya OpasawaschaiDepartment of Microbiology, Faculty of Science, Mahidol University, Bangkok, Thailand.
Pisut PongchaikulDepartment of Microbiology, Faculty of Science, Mahidol University, Bangkok, Thailand.
Nattaya TangthawornchaikulMedical Biotechnology Unit, National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Pathumthani, Thailand.
Sirijitt VasanawathanaDepartment of Pediatrics, Khon Kaen Hospital, Khon Kaen, Thailand.
Wannee LimpitikulDepartment of Pediatrics, Songkhla hospital, Songkhla, Thailand.
Prida MalasitCenter of Emerging and Neglected Infectious Diseases, Mahidol University, Bangkok, Thailand; Medical Biotechnology Unit, National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Pathumthani, Thailand; Dengue Hemorrhagic Fever Research Unit, Office for Research and Development, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Thaneeya DuangchindaCenter of Emerging and Neglected Infectious Diseases, Mahidol University, Bangkok, Thailand; Medical Biotechnology Unit, National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, Pathumthani, Thailand.
Gavin ScreatonDivision of Immunology and Inflammation, Department of Medicine, Hammersmith campus, Imperial College London, London, United Kingdom.
Juthathip MongkolsapayaCenter of Emerging and Neglected Infectious Diseases, Mahidol University, Bangkok, Thailand; Dengue Hemorrhagic Fever Research Unit, Office for Research and Development, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailand; Division of Immunology and Inflammation, Department of Medicine, Hammersmith campus, Imperial College London, London, United Kingdom.
Mahidol University · THHammersmith Hospital · GBNational Center for Genetic Engineering and Biotechnology · THKhon Kaen University · THNational Science and Technology Development Agency · TH

Funding

Medical Research Council G0400720Medical Research Council G0600000Medical Research Council G0801508Wellcome Trust 095541
6 · The paper itself

Abstract

backgroundDengue viral infection is a global health threat without vaccine or specific treatment. The clinical outcome varies from asymptomatic, mild dengue fever (DF) to severe dengue hemorrhagic fever (DHF). While adaptive immune responses were found to be detrimental in the dengue pathogenesis, the roles of earlier innate events remain largely uninvestigated. Invariant natural killer T (iNKT) cells represent innate-like T cells that could dictate subsequent adaptive response but their role in human dengue virus infection is not known. We hypothesized that iNKT cells play a role in human dengue infection.

methodsBlood samples from a well-characterized cohort of children with DF, DHF, in comparison to non-dengue febrile illness (OFI) and healthy controls at various time points were studied. iNKT cells activation were analyzed by the expression of CD69 by flow cytometry. Their cytokine production was then analyzed after α-GalCer stimulation. Further, the CD1d expression on monocytes, and CD69 expression on conventional T cells were measured.

resultsiNKT cells were activated during acute dengue infection. The level of iNKT cell activation associates with the disease severity. Furthermore, these iNKT cells had altered functional response to subsequent ex vivo stimulation with α-GalCer. Moreover, during acute dengue infection, monocytic CD1d expression was also upregulated and conventional T cells also became activated.

conclusioniNKT cells might play an early and critical role in the pathogenesis of severe dengue viral infection in human. Targeting iNKT cells and CD1d serve as a potential therapeutic strategy for severe dengue infection in the future.

Indexed as

Immunity, InnateLymphocyte ActivationAdolescentAntigens, CDAntigens, CD1dAntigens, Differentiation, T-LymphocyteCase-Control StudiesCD69 AntigensChildChild, PreschoolCytokinesDengueDengue VirusFemaleFlow CytometryGalactosylceramidesalpha-galactosylceramideAntigens, CDAntigens, CD1dAntigens, Differentiation, T-LymphocyteCD1D protein, humanCD69 AntigensCytokinesGalactosylceramidesLectins, C-Type

Identifiers

PMID24945350
PMCPMC4063705
OpenAlexW2071288084

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.