Tehran University of Medical Sciences

Science Communicator Platform

Stay connected! Follow us on X network (Twitter):
Share this content! On (X network) By
Efficacy of Disease Modifying Therapies in Progressive Ms and How Immune Senescence May Explain Their Failure Publisher



Manouchehri N1 ; Salinas VH1 ; Rabi Yeganeh N2 ; Pitt D3 ; Hussain RZ1 ; Stuve O1, 4
Authors
Show Affiliations
Authors Affiliations
  1. 1. Department of Neurology, The University of Texas Southwestern Medical Center, Dallas, TX, United States
  2. 2. Department of Radiopharmacy, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Department of Neurology, Yale University, New Haven, CT, United States
  4. 4. Neurology Section, VA North Texas Health Care System, Medical Service Dallas, Veterans Affairs Medical Center, Dallas, TX, United States

Source: Frontiers in Neurology Published:2022


Abstract

The advent of disease modifying therapies (DMT) in the past two decades has been the cornerstone of successful clinical management of multiple sclerosis (MS). Despite the great strides made in reducing the relapse frequency and occurrence of new signal changes on neuroimaging in patients with relapsing remitting MS (RRMS) by approved DMT, it has been challenging to demonstrate their effectiveness in non-active secondary progressive MS (SPMS) and primary progressive MS (PPMS) disease phenotypes. The dichotomy of DMT effectiveness between RRMS and progressive MS informs on distinct pathogeneses of the different MS phenotypes. Conversely, factors that render patients with progressive MS resistant to therapy are not understood. Thus far, age has emerged as the main correlate of the transition from RRMS to SPMS. Whether it is aging and age-related factors or the underlying immune senescence that qualitatively alter immune responses as the disease transitions to SPMS, that diminish DMT effectiveness, or both, is currently not known. Here, we will discuss the role of immune senescence on different arms of the immune system, and how it may explain relative DMT resistance. Copyright © 2022 Manouchehri, Salinas, Rabi Yeganeh, Pitt, Hussain and Stuve.
Other Related Docs
11. Aging and Cancer Prognosis, Cancer Immunology: Bench to Bedside Immunotherapy of Cancers# Second Edition (2020)
13. B Cells in Multiple Sclerosis Therapy—A Comprehensive Review, Acta Neurologica Scandinavica (2018)
24. Caspase-1 Inhibition Prevents Glial Inflammasome Activation and Pyroptosis in Models of Multiple Sclerosis, Proceedings of the National Academy of Sciences of the United States of America (2018)
25. The Emerging Role of Lncrnas in Multiple Sclerosis, Journal of Neuroimmunology (2020)
27. Autoimmune Diseases, Clinical Immunology (2022)
29. Cellular Senescence Implication in Mustard Keratopathy, Experimental Eye Research (2023)
36. Introduction to the Neuroimmunology of Multiple Sclerosis, Translational Neuroimmunology: Multiple Sclerosis: Volume 8 (2023)