Literature DB >> 33651184

Checkpoint Molecules in Rheumatology-or the Benefits of Being Exhausted.

Stinne Ravn Greisen1,2, Bent Deleuran3,4.   

Abstract

PURPOSE OF REVIEW: This review will focus on the most common co-inhibitory molecules, emphasizing the importance of these in relation to rheumatic disease. RECENT
FINDINGS: Checkpoint molecules are pivotal in determining the outcome of antigen activation. Checkpoint molecules consist of co-stimulatory and co-inhibitory molecules, where the first activates and the latter inhibits the antigen presentation process. Studies show that increased activity of co-inhibitory molecules is associated with a good prognosis in rheumatic diseases. Opposite, when cancer patients are treated with antibodies blocking the inhibitory pathways, autoimmune diseases, including arthritis, develop as immune-related adverse events (IrAE). This emphasizes the importance of these pathways in autoimmune disease. Co-inhibitory molecules are becoming increasingly interesting as future treatment targets in rheumatic conditions. Treatments with antibodies blocking these pathways result in IrAE, often manifesting as autoimmune rheumatic diseases. Therefore, a need to get acquainted with these molecules is growing so we can cope with future challenges in rheumatic diseases.

Entities:  

Keywords:  Autoimmunity; Co-inhibitory molecules; Exhausted T cells; Rheumatic diseases

Year:  2021        PMID: 33651184     DOI: 10.1007/s11926-021-00991-2

Source DB:  PubMed          Journal:  Curr Rheumatol Rep        ISSN: 1523-3774            Impact factor:   4.592


  78 in total

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5.  Association of a BTLA gene polymorphism with the risk of rheumatoid arthritis.

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Review 6.  Defining 'T cell exhaustion'.

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Journal:  Nat Rev Immunol       Date:  2019-09-30       Impact factor: 53.106

Review 7.  Molecular and cellular insights into T cell exhaustion.

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Journal:  Nat Rev Immunol       Date:  2013-03-08       Impact factor: 53.106

9.  PD-1 blockade partially recovers dysfunctional virus-specific B cells in chronic hepatitis B infection.

Authors:  Loghman Salimzadeh; Nina Le Bert; Charles-A Dutertre; Upkar S Gill; Evan W Newell; Christian Frey; Magdeleine Hung; Nikolai Novikov; Simon Fletcher; Patrick Tf Kennedy; Antonio Bertoletti
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Authors:  Eoin F McKinney; James C Lee; David R W Jayne; Paul A Lyons; Kenneth G C Smith
Journal:  Nature       Date:  2015-06-29       Impact factor: 49.962

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