Evidence map›Paper›PMID 29672707›Full record

ArticleThe Journal of infectious diseases2018

Longitudinal Study of Cellular and Systemic Cytokine Signatures to Define the Dynamics of a Balanced Immune Environment During Disease Manifestation in Zika Virus-Infected Patients.

Fok-Moon Lum, David C B Lye, Jeslin J L Tan, Bernett Lee, Po-Ying Chia, Tze-Kwang Chua, Siti N Amrun, Yiu-Wing Kam, Wearn-Xin Yee, Wei-Ping Ling and 7 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
6.9field-weighted citation impact, top 3% 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

32 citing papers in PubMed, 52 citations in OpenAlex.

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  16. Host immune response against DENV and ZIKV infections.Frontiers in cellular and infection microbiology · 2022
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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

17 authors at 7 institutions in 2 countries.

Fok-Moon LumSingapore Immunology Network, Agency for Science, Technology, and Research, Singapore.
David C B LyeCommunicable Diseases Centre, Institute of Infectious Diseases and Epidemiology, Tan Tock Seng Hospital, Singapore.
Jeslin J L TanSingapore Immunology Network, Agency for Science, Technology, and Research, Singapore.
Bernett LeeSingapore Immunology Network, Agency for Science, Technology, and Research, Singapore.
Po-Ying ChiaCommunicable Diseases Centre, Institute of Infectious Diseases and Epidemiology, Tan Tock Seng Hospital, Singapore.
Tze-Kwang ChuaSingapore Immunology Network, Agency for Science, Technology, and Research, Singapore.
Siti N AmrunSingapore Immunology Network, Agency for Science, Technology, and Research, Singapore.
Yiu-Wing KamSingapore Immunology Network, Agency for Science, Technology, and Research, Singapore.
Wearn-Xin YeeSingapore Immunology Network, Agency for Science, Technology, and Research, Singapore.
Wei-Ping LingCommunicable Diseases Centre, Institute of Infectious Diseases and Epidemiology, Tan Tock Seng Hospital, Singapore.
Vanessa W X LimCommunicable Diseases Centre, Institute of Infectious Diseases and Epidemiology, Tan Tock Seng Hospital, Singapore.
Vincent J X PangCommunicable Diseases Centre, Institute of Infectious Diseases and Epidemiology, Tan Tock Seng Hospital, Singapore.
Linda K LeeCommunicable Diseases Centre, Institute of Infectious Diseases and Epidemiology, Tan Tock Seng Hospital, Singapore.
Esther W H MokSingapore Immunology Network, Agency for Science, Technology, and Research, Singapore.
Chia-Yin ChongKK Women's and Children's Hospital, Singapore.
Yee-Sin LeoCommunicable Diseases Centre, Institute of Infectious Diseases and Epidemiology, Tan Tock Seng Hospital, Singapore.
Lisa F P NgSingapore Immunology Network, Agency for Science, Technology, and Research, Singapore.
Agency for Science, Technology and Research · SGTan Tock Seng Hospital · SGSingapore Immunology Network · SGKK Women's and Children's Hospital · SGNanyang Technological University · SGNational University Health System · SGSingapore College of Traditional Chinese Medicine · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Since its unexpected reemergence, Zika virus (ZIKV) has caused numerous outbreaks globally. This study characterized the host immune responses during ZIKV infection. Methods: Patient samples were collected longitudinally during the acute, convalescence and recovery phases of ZIKV infection over 6 months during the Singapore outbreak in late 2016. Plasma immune mediators were profiled via multiplex microbead assay, while changes in blood cell numbers were determined with immunophenotyping. Results: Data showed the involvement of various immune mediators during acute ZIKV infection accompanied by a general reduction in blood cell numbers for all immune subsets except CD14+ monocytes. Importantly, viremic patients experiencing moderate symptoms had significantly higher quantities of interferon γ-induced protein 10, monocyte chemotactic protein 1, interleukin 1 receptor antagonist, interleukin 8, and placental growth factor 1, accompanied by reduced numbers of peripheral CD8+ T cells, CD4+ T cells, and double-negative T cells. Levels of T-cell associated mediators, including interferon γ-induced protein 10, interferon γ, and interleukin 10, were high in recovery phases of ZIKV infection, suggesting a functional role for T cells. The identification of different markers at specific disease phases emphasizes the dynamics of a balanced cytokine environment in disease progression. Conclusions: This is the first comprehensive study that highlights specific cellular changes and immune signatures during ZIKV disease progression, and it provides valuable insights into ZIKV immunopathogenesis.

Indexed as

AdolescentAdultAgedCytokinesDisease OutbreaksFemaleHumansImmunoassayLongitudinal StudiesMaleMiddle AgedPlasmaSingaporeT-Lymphocyte SubsetsYoung AdultZika VirusCytokines

Identifiers

PMID29672707
PMCPMC6057545
OpenAlexW2801013503

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.