4.8 Review

Potential for Targeting Myeloid Cells in Controlling CNS Inflammation

Journal

FRONTIERS IN IMMUNOLOGY
Volume 11, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2020.571897

Keywords

myeloid cels; multiple sclerosis; chemokines; GM-CSF; miRNAs; nanoparticles; M-CSF

Categories

Funding

  1. NIH [EB-013198, NS-026543]
  2. Johnnie Walker's MS Foundation
  3. David & Amy Fulton Foundation
  4. Crammer Family Foundation
  5. National Multiple Sclerosis Society [RG 4952-A-5]
  6. National Multiple Sclerosis Society Post-Doctoral Fellowship [G-1508-05965]
  7. National Multiple Sclerosis Society Pilot Research Grant [PP-1905-33998]
  8. Cour PharmaceuticalDevelopment Company

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Multiple Sclerosis (MS) is characterized by immune cell infiltration to the central nervous system (CNS) as well as loss of myelin. Characterization of the cells in lesions of MS patients revealed an important accumulation of myeloid cells such as macrophages and dendritic cells (DCs). Data from the experimental autoimmune encephalomyelitis (EAE) model of MS supports the importance of peripheral myeloid cells in the disease pathology. However, the majority of MS therapies focus on lymphocytes. As we will discuss in this review, multiple strategies are now in place to target myeloid cells in clinical trials. These strategies have emerged from data in both human and mouse studies. We discuss strategies targeting myeloid cell migration, growth factors and cytokines, biological functions (with a focus on miRNAs), and immunological activities (with a focus on nanoparticles).

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