Literature DB >> 29424301

Novel Therapeutic Approaches in Rheumatoid Arthritis: Role of Janus Kinases Inhibitors.

Felice Rivellese1,2, Antonio Lobasso1, Letizia Barbieri1, Bianca Liccardo1, Amato de Paulis1,3, Francesca Wanda Rossi1,3.   

Abstract

Rheumatoid Arthritis (RA) is a chronic inflammatory disease characterized by synovial inflammation and hyperplasia, autoantibody production, cartilage and bone destruction and several systemic features. Cardiovascular, pulmonary, psychological, and muscle involvement are the main comorbidities of RA and are responsible for the severity of the disease and long-term prognosis. Pharmacological treatment of rheumatic diseases has evolved remarkably over the past years. In addition, the widespread adoption of treat to target and tight control strategies has led to a substantial improvement of outcomes, so that drug-free remission is nowadays a realistic goal in the treatment of RA. However, despite the availability of multiple therapeutic options, up to 40% of patients do not respond to current treatments, including biologics. Small-molecule therapies offer an alternative to biological therapies for the treatment of inflammatory diseases. In the past 5 years, a number of small-molecule compounds targeting Janus Kinases (JAKs) have been developed. Since JAKs are essential for cell signaling in immune cells, in particular controlling the response to many cytokines, their inhibitors quickly became a promising class of oral therapeutics that proved effective in the treatment of RA. Tofacitinib is the first Janus Kinase (JAK) inhibitor approved for the treatment of RA, followed more recently by baricitinib. Several other JAK inhibitors, are currently being tested in phase II and III trials for the treatment of a different autoimmune diseases. Most of these compounds exhibit an overall acceptable safety profile similar to that of biologic agents, with infections being the most frequent adverse event. Apart from tofacitinib, safety data on other JAK inhibitors are still limited. Long-term follow-up and further research are needed to evaluate the general safety profile and the global risk of malignancy of these small molecules, although no clear association with malignancy has been reported to date. Here, we will review the main characteristics of JAK inhibitors, including details on their molecular targets and on the clinical evidences obtained so far in the treatment of RA. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Entities:  

Keywords:  Rheumatoid arthritis; chronic disease; drug free remission; hyperplasia; inflammation; janus kinase inhibitors.

Mesh:

Substances:

Year:  2019        PMID: 29424301     DOI: 10.2174/0929867325666180209145243

Source DB:  PubMed          Journal:  Curr Med Chem        ISSN: 0929-8673            Impact factor:   4.530


  7 in total

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2.  Baricitinib, a Janus kinase inhibitor, in the treatment of rheumatoid arthritis: a systematic literature review and meta-analysis of randomized controlled trials.

Authors:  Sumit Kunwar; Christopher E Collins; Florina Constantinescu
Journal:  Clin Rheumatol       Date:  2018-07-13       Impact factor: 2.980

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Review 4.  Mast Cells in Early Rheumatoid Arthritis.

Authors:  Felice Rivellese; Francesca Wanda Rossi; Maria Rosaria Galdiero; Costantino Pitzalis; Amato de Paulis
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5.  Takinib Inhibits Inflammation in Human Rheumatoid Arthritis Synovial Fibroblasts by Targeting the Janus Kinase-Signal Transducer and Activator of Transcription 3 (JAK/STAT3) Pathway.

Authors:  Paul M Panipinto; Anil K Singh; Farheen S Shaikh; Ruby J Siegel; Mukesh Chourasia; Salahuddin Ahmed
Journal:  Int J Mol Sci       Date:  2021-11-22       Impact factor: 5.923

6.  Folate receptor-targeting mesoporous silica-coated gold nanorod nanoparticles for the synergistic photothermal therapy and chemotherapy of rheumatoid arthritis.

Authors:  Xiangyu Li; Yufei Hou; Xiangxue Meng; Ge Li; Fei Xu; Lesheng Teng; Fengying Sun; Youxin Li
Journal:  RSC Adv       Date:  2021-01-18       Impact factor: 3.361

7.  Pyridinone Derivatives as Interesting Formyl Peptide Receptor (FPR) Agonists for the Treatment of Rheumatoid Arthritis.

Authors:  Letizia Crocetti; Claudia Vergelli; Gabriella Guerrini; Maria Paola Giovannoni; Liliya N Kirpotina; Andrei I Khlebnikov; Carla Ghelardini; Lorenzo Di Cesare Mannelli; Elena Lucarini; Igor A Schepetkin; Mark T Quinn
Journal:  Molecules       Date:  2021-10-30       Impact factor: 4.411

  7 in total

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