Immune Netw.  2016 Feb;16(1):44-51. 10.4110/in.2016.16.1.44.

Dendritic Cell-based Immunotherapy for Rheumatoid Arthritis: from Bench to Bedside

Affiliations
  • 1Department of Biological Science, Sungkyunkwan University, Suwon 16419, Korea. ysbae04@skku.edu
  • 2Department of Medicine, Surgery and Obstetrics, Faculty of Animal Science and Veterinary Medicine, Patuakhali Science and Technology University, Khanpura, Babugonj-8210, Barisal, Bangladesh.

Abstract

Dendritic cells (DCs) are professional antigen presenting cells, and play an important role in the induction of antigen-specific adaptive immunity. However, some DC populations are involved in immune regulation and immune tolerance. These DC populations are believed to take part in the control of immune exaggeration and immune disorder, and maintain immune homeostasis in the body. Tolerogenic DCs (tolDCs) can be generated in vitro by genetic or pharmacological modification or by controlling the maturation stages of cytokine-derived DCs. These tolDCs have been investigated for the treatment of rheumatoid arthritis (RA) in experimental animal models. In the last decade, several in vitro and in vivo approaches have been translated into clinical trials. As of 2015, three tolDC trials for RA are on the list of ClinicalTrial.gov (www.clinicaltrials.gov). Other trials for RA are in progress and will be listed soon. In this review, we discuss the evolution of tolDC-based immunotherapy for RA and its limitations and future prospects.

Keyword

Tolerogenic dendritic cell (tolDC); Immunotherapy; Tolerance; Rheumatoid arthritis (RA); Mouse collagen-induced arthritis (CIA); Clinical study; Treg; Limitation; Future

MeSH Terms

Adaptive Immunity
Antigen-Presenting Cells
Arthritis, Rheumatoid*
Dendritic Cells
Homeostasis
Immune System Diseases
Immune Tolerance
Immunotherapy*
Models, Animal

Cited by  1 articles

Generation, Characteristics and Clinical Trials of Ex Vivo Generated Tolerogenic Dendritic Cells
Sang-Hyun Kim, Ho-Hyun Jung, Chong-Kil Lee
Yonsei Med J. 2018;59(7):807-815.    doi: 10.3349/ymj.2018.59.7.807.


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