Evidence map›Paper›PMID 28754958›Full record

ArticleScientific reports2017

A study on the risk of fungal infection with tofacitinib (CP-690550), a novel oral agent for rheumatoid arthritis.

Yong Chen, Fang-Yuan Gong, Zhen-Jun Li, Zheng Gong, Zhe Zhou, Shu-Yan Ma, Xiao-Ming Gao

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 2 pooled it
1.8field-weighted citation impact, top 16% 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

18 citing papers in PubMed, 2 syntheses or guidelines pooled it, 39 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. The infection risks of JAK inhibition.Expert review of clinical immunology · 2022
    Article
  10. The emerging role of neutrophil extracellular traps in fungal infection.Frontiers in cellular and infection microbiology · 2022
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Risks of Ruxolitinib inOpen forum infectious diseases · 2017
    Article
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

7 authors at 2 institutions in 1 country.

Yong ChenInstitute of Biology and Medical Sciences (IBMS), School of Biology and Basic Medical Sciences, Soochow University, Suzhou, China.
Fang-Yuan GongInstitute of Biology and Medical Sciences (IBMS), School of Biology and Basic Medical Sciences, Soochow University, Suzhou, China. gongfangyuan@suda.edu.cn.
Zhen-Jun LiSuzhou Kowloon Hospital, Shanghai Jiao Tong University School of Medicine, Suzhou, China.
Zheng GongInstitute of Biology and Medical Sciences (IBMS), School of Biology and Basic Medical Sciences, Soochow University, Suzhou, China.
Zhe ZhouInstitute of Biology and Medical Sciences (IBMS), School of Biology and Basic Medical Sciences, Soochow University, Suzhou, China.
Shu-Yan MaInstitute of Biology and Medical Sciences (IBMS), School of Biology and Basic Medical Sciences, Soochow University, Suzhou, China.
Xiao-Ming GaoInstitute of Biology and Medical Sciences (IBMS), School of Biology and Basic Medical Sciences, Soochow University, Suzhou, China. xmgao@suda.edu.cn.
Soochow University · CNShanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tofacitinib (CP-690550), an oral Janus kinase inhibitor, has shown significant efficacy in the treatment of rheumatoid arthritis through blocking the signaling pathways of pro-inflammatory cytokines. However, recent evidence suggests that long-term tofacitinib treatment is associated with increased risk of infection (e.g. tuberculosis) in patients. In the present study, we illustrate that tofacitinib administration significantly reduced the survival rate of mice given lethal or sub-lethal dose challenge with Candida albicans. This was related to the ability of tofacitinib to reverse TNFα- and IFNγ-enhanced candidacidal activity of murine polymorph nuclear cells (PMNs) and also to suppress chemokine CXCL5 expression and PMN infiltration in the infected tissues of mice. More importantly, tofacitinib significantly antagonized the ability of TNFα, IFNγ and GM-CSF to boost human PMNs in phagocytosis and direct killing of C. albicans in vitro. It also down-regulated reactive oxygen production and neutrophil extracellular trap formation by human PMNs stimulated with yeast-derived β-glucans in the presence of TNFα, IFNγ or GM-CSF. Our data emphasizes a significantly increased risk for opportunistic fungal infection associated long-term tofacitinib treatment in humans, likely through antagonizing the PMN-boosting effect of pro-inflammatory cytokines.

Indexed as

Administration, OralAdultAnimalsArthritis, RheumatoidCandida albicansCandidiasisDisease SusceptibilityFemaleHumansMice, Inbred BALB CNeutrophil ActivationNeutrophilsPhagocytosisPiperidinesPyrimidinesPyrrolesPiperidinesPyrimidinesPyrrolestofacitinib

Identifiers

PMID28754958
PMCPMC5533717
OpenAlexW2737740473

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.