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Immune checkpoint failures in inflammatory myopathies: An overview

Overview of attention for article published in Autoimmunity Reviews, June 2018
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Title
Immune checkpoint failures in inflammatory myopathies: An overview
Published in
Autoimmunity Reviews, June 2018
DOI 10.1016/j.autrev.2018.01.026
Pubmed ID
Authors

Sandrine Herbelet, Jan L De Bleecker

Abstract

Dermatomyositis (DM), polymyositis (PM), inclusion bosy myositis (IBM), immune mediated necrotizing myopathy (IMNM) and overlap myositis (OM) are classified as inflammatory myopathies (IM) with involvement of autoimmune features such as autoreactive lymphocytes and autoantibodies. Autoimmunity can be defined as a loss in self-tolerance and attack of autoantigens by the immune system. Self-tolerance is achieved by a group of immune mechanisms occurring in central and periphal lymphoid organs and tissues, called immune checkpoints, that work in synergy to protect the body from harmful immune reactions. Autoimmune disorders appear when immune checkpoints fail. In this review, the different immune checkpoint failures are discussed in DM, PM, IBM and IMNM. Exploring research contribution in each of these immune checkpoints might help to highlight research perspectives in the field and obtain a more complete picture of IM disease pathology.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 37 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 37 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 6 16%
Student > Postgraduate 6 16%
Student > Ph. D. Student 5 14%
Student > Master 5 14%
Student > Bachelor 4 11%
Other 4 11%
Unknown 7 19%
Readers by discipline Count As %
Medicine and Dentistry 16 43%
Biochemistry, Genetics and Molecular Biology 4 11%
Immunology and Microbiology 3 8%
Neuroscience 3 8%
Agricultural and Biological Sciences 2 5%
Other 1 3%
Unknown 8 22%