Evidence map›Paper›PMID 34215212›Full record

ArticleBMC infectious diseases2021

Comparative cytokine profiling identifies common and unique serum cytokine responses in acute chikungunya and dengue virus infection.

Rama Dhenni, Benediktus Yohan, Bachti Alisjahbana, Anton Lucanus, Silvita Fitri Riswari, Dewi Megawati, Sotianingsih Haryanto, Dekrit Gampamole, Rahma F Hayati, Kartika Sari and 3 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in BMC infectious diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 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

13 authors at 5 institutions in 2 countries.

Rama DhenniEijkman Institute for Molecular Biology, Jakarta, Indonesia.
Benediktus YohanEijkman Institute for Molecular Biology, Jakarta, Indonesia.
Bachti AlisjahbanaFaculty of Medicine, Universitas Padjadjaran, Bandung, Indonesia.
Anton LucanusSchool of Anatomy, Physiology and Human Biology, University of Western Australia, Perth, Australia.
Silvita Fitri RiswariFaculty of Medicine, Universitas Padjadjaran, Bandung, Indonesia.
Dewi MegawatiFaculty of Medicine and Health Sciences, Warmadewa University, Denpasar, Bali, Indonesia.
Sotianingsih HaryantoSiloam Hospital, Jambi, Indonesia.
Dekrit GampamoleBethesda Hospital, Tomohon, Indonesia.
Rahma F HayatiEijkman Institute for Molecular Biology, Jakarta, Indonesia.
Kartika SariFaculty of Medicine and Health Sciences, Warmadewa University, Denpasar, Bali, Indonesia.
Ni Putu Diah WitariFaculty of Medicine and Health Sciences, Warmadewa University, Denpasar, Bali, Indonesia.
Khin Saw Aye MyintEijkman Institute for Molecular Biology, Jakarta, Indonesia.
R Tedjo SasmonoEijkman Institute for Molecular Biology, Jakarta, Indonesia. sasmono@eijkman.go.id.ORCID http://orcid.org/0000-0003-0986-2590
Eijkman Institute for Molecular Biology · IDWarmadewa University · IDPadjadjaran University · IDJambi University · IDThe University of Western Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInfection by chikungunya (CHIKV) and dengue virus (DENV) can cause a wide spectrum of clinical features, many of which are undifferentiated. Cytokines, which broadly also include chemokines and growth factors, have been shown to play a role in protective immunity as well as DENV and CHIKV pathogenesis. However, differences in cytokine response to both viruses remain poorly understood, especially in patients from countries where both viruses are endemic. Our study is therefore aimed to provide a comparative profiling of cytokine response induced by acute DENV and CHIKV infections in patients with similar disease stages and in experimental in vitro infections.

methodsBy using multiplex immunoassay, we compared host cytokine profiles between acute CHIKV and DENV infections by analysing serum cytokine levels of IL-1α, IL-4, IL-5, IL-8, IL-13, RANTES, MCP-3, eotaxin, PDGF-AB/BB, and FGF-2 from the sera of acute chikungunya and dengue fever patients. We further investigated the cytokine profile responses using experimental in vitro CHIKV and DENV infections of peripheral blood mononuclear cells (PBMCs).

resultsWe found that both CHIKV and DENV-infected patients had an upregulated level of IL-8 and IL-4, with the highest IL-4 level observed in DENV-2 infected patients. Higher IL-8 level was also correlated with lower platelet count in dengue patients. IL-13 and MCP-3 downregulation was observed only in chikungunya patients, while conversely PDGF-AB/BB and FGF-2 downregulation was unique in dengue patients. Age-associated differential expression of IL-13, MCP-3, and IL-5 was also observed, while distinct kinetics of IL-4, IL-8, and FGF-2 expression between CHIKV and DENV-infected patients were identified. Furthermore, the unique pattern of IL-8, IL-13 and MCP-3, but not IL-4 expression was also recapitulated using experimental in vitro infection in PBMCs.

conclusionsTaken together, our study identified common cytokine response profile characterized by upregulation of IL-8 and IL-4 between CHIKV and DENV infection. Downregulation of IL-13 and MCP-3 was identified as a unique cytokine response profile of acute CHIKV infection, while distinct downregulation of PDGF-AB/BB and FGF-2 characterized the response from acute DENV infection. Our study provides an important overview of the host cytokine responses between CHIKV and DENV infection, which is important to further understand the mechanism and pathology of these diseases.

Indexed as

AdolescentAdultAgedChikungunya FeverChikungunya virusChildChild, PreschoolCross-Sectional StudiesCytokinesDengueDengue VirusFemaleHumansIndonesiaInfantMaleCytokinesChikungunyaCytokineDengueHost response

Identifiers

PMID34215212
PMCPMC8254284
OpenAlexW3174851123

What OpenQuestion holds

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LicenceCC BY
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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.