Evidence map›Paper›PMID 34609725›Full record

ReviewDrugs2021

Bruton's Tyrosine Kinase Inhibition as an Emerging Therapy in Systemic Autoimmune Disease.

Stefan F H Neys, Jasper Rip, Rudi W Hendriks, Odilia B J Corneth

Open access · hybridAbstract readReview
In one paragraph

Review in Drugs, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
5.3field-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

30 citing papers in PubMed, 51 citations in OpenAlex.

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  20. Multiple Sclerosis: Inflammatory and Neuroglial Aspects.Current issues in molecular biology · 2023
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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

4 authors at 1 institution in 1 country.

Stefan F H NeysDepartment of Pulmonary Medicine, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.
Jasper RipDepartment of Pulmonary Medicine, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.
Rudi W Hendriks *Department of Pulmonary Medicine, Erasmus MC, University Medical Center, Rotterdam, The Netherlands. r.hendriks@erasmusmc.nl.ORCID http://orcid.org/0000-0003-2291-0382
Odilia B J Corneth *Department of Pulmonary Medicine, Erasmus MC, University Medical Center, Rotterdam, The Netherlands. o.corneth@erasmusmc.nl.
Erasmus MC · NL

Funding

ReumaNederland 19-1-201
6 · The paper itself

Abstract

Systemic autoimmune disorders are complex heterogeneous chronic diseases involving many different immune cells. A significant proportion of patients respond poorly to therapy. In addition, the high burden of adverse effects caused by "classical" anti-rheumatic or immune modulatory drugs provides a need to develop more specific therapies that are better tolerated. Bruton's tyrosine kinase (BTK) is a crucial signaling protein that directly links B-cell receptor (BCR) signals to B-cell activation, proliferation, and survival. BTK is not only expressed in B cells but also in myeloid cells, and is involved in many different signaling pathways that drive autoimmunity. This makes BTK an interesting therapeutic target in the treatment of autoimmune diseases. The past decade has seen the emergence of first-line BTK small-molecule inhibitors with great efficacy in the treatment of B-cell malignancies, but with unfavorable safety profiles for use in autoimmunity due to off-target effects. The development of second-generation BTK inhibitors with superior BTK specificity has facilitated the investigation of their efficacy in clinical trials with autoimmune patients. In this review, we discuss the role of BTK in key signaling pathways involved in autoimmunity and provide an overview of the different inhibitors that are currently being investigated in clinical trials of systemic autoimmune diseases, including rheumatoid arthritis and systemic lupus erythematosus, as well as available results from completed trials.

Indexed as

Agammaglobulinaemia Tyrosine KinaseAutoimmune DiseasesAutoimmunityB-LymphocytesClinical Trials as TopicHumansLymphocyte ActivationReceptors, Antigen, B-CellSignal TransductionAgammaglobulinaemia Tyrosine KinaseReceptors, Antigen, B-Cell

Identifiers

PMID34609725
PMCPMC8491186
OpenAlexW3203276822

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.