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Janus Kinase Inhibitor Baricitinib Modulates Human Innate and Adaptive Immune System

Overview of attention for article published in Frontiers in immunology, June 2018
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  • In the top 25% of all research outputs scored by Altmetric
  • Good Attention Score compared to outputs of the same age (75th percentile)
  • Good Attention Score compared to outputs of the same age and source (76th percentile)

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7 X users
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1 patent

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103 Dimensions

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Title
Janus Kinase Inhibitor Baricitinib Modulates Human Innate and Adaptive Immune System
Published in
Frontiers in immunology, June 2018
DOI 10.3389/fimmu.2018.01510
Pubmed ID
Authors

Satoshi Kubo, Shingo Nakayamada, Kei Sakata, Yukihiro Kitanaga, Xiaoxue Ma, Seunghyun Lee, Akina Ishii, Kaoru Yamagata, Kazuhisa Nakano, Yoshiya Tanaka

Abstract

The purpose of this study was to elucidate the mechanism of action of baricitinib on Janus kinase (JAK)/signal transducer and activator of transcription (STAT) signaling, which involves in human innate and adaptive immune system. The effects of baricitinib were evaluated using human monocyte-derived dendritic cells (MoDCs), plasmacytoid dendritic cells (pDCs), B cells, and T cells. Baricitinib concentration-dependently suppressed the expression of CD80/CD86 on MoDCs and the production of type-I interferon (IFN) by pDCs. Baricitinib also suppressed the differentiation of human B cells into plasmablasts by B cell receptor and type-I IFN stimuli and inhibited the production of interleukin (IL)-6 from B cells. Human CD4+ T cells proliferated after T cell receptor stimulation with anti-CD3 and anti-CD28 antibody; however, such proliferation was suppressed by baricitinib in a concentration-dependent manner. In addition, baricitinib inhibited Th1 differentiation after IL-12 stimulation and Th17 differentiation by TGF-β1, IL-6, IL-1β, and IL-23 stimulation. Tofacitinib showed similar effects in these experiments. In naive CD4+ T cells, IFN-α and IFN-γ induced phosphorylation of STAT1, which was inhibited by baricitinib and tofacitinib. Furthermore, IL-6-induced phosphorylation of STAT1 and STAT3 was also inhibited by JAK inhibitors. In conclusion, the results indicated that baricitinib suppresses the differentiation of plasmablasts, Th1 and Th17 cells, as well as innate immunity, such as the T cell stimulatory capacity of dendritic cells. Thus, JAK inhibitors can be potentially clinically effective not only in rheumatoid arthritis but other immune-related diseases.

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X Demographics

X Demographics

The data shown below were collected from the profiles of 7 X users who shared this research output. Click here to find out more about how the information was compiled.
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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 93 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 93 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 11 12%
Student > Ph. D. Student 8 9%
Student > Bachelor 8 9%
Student > Postgraduate 6 6%
Student > Doctoral Student 6 6%
Other 22 24%
Unknown 32 34%
Readers by discipline Count As %
Medicine and Dentistry 15 16%
Biochemistry, Genetics and Molecular Biology 11 12%
Agricultural and Biological Sciences 7 8%
Immunology and Microbiology 6 6%
Pharmacology, Toxicology and Pharmaceutical Science 5 5%
Other 10 11%
Unknown 39 42%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 8. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 21 July 2022.
All research outputs
#4,661,764
of 25,385,509 outputs
Outputs from Frontiers in immunology
#5,027
of 31,537 outputs
Outputs of similar age
#83,421
of 342,889 outputs
Outputs of similar age from Frontiers in immunology
#168
of 727 outputs
Altmetric has tracked 25,385,509 research outputs across all sources so far. Compared to these this one has done well and is in the 81st percentile: it's in the top 25% of all research outputs ever tracked by Altmetric.
So far Altmetric has tracked 31,537 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 8.4. This one has done well, scoring higher than 83% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 342,889 tracked outputs that were published within six weeks on either side of this one in any source. This one has done well, scoring higher than 75% of its contemporaries.
We're also able to compare this research output to 727 others from the same source and published within six weeks on either side of this one. This one has done well, scoring higher than 76% of its contemporaries.