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B7 immune checkpoint family members as putative therapeutics in autoimmune disease: An updated overview.

Katayoun DolatkhahNazila AlizadehHanieh Mohajjel-ShojaMahdi Abdoli ShadbadKhalil HajiasgharzadehLeili Aghebati-MalekiAmir BaghbanzadehNegar HosseinkhaniNoora Karim AhangarBehzad Baradaran
Published in: International journal of rheumatic diseases (2022)
Autoimmune diseases, especially among young people in the US, are one of the leading causes of morbidity and death. The immune responses are the fundamental pathogenicity of autoimmune disorders. The equilibrium between stimulatory and inhibitory signals is critical for the stimulation, migration, survival, and T cell-related immune responses. The B7 family can substantially regulate T cell-mediated immune responses. Nevertheless, recent breakthroughs in immune checkpoint blockade in cancer immunotherapy have facilitated autoimmune diseases, especially among the prone populations. In the current study, we tried to concisely review the role of the B7 family in regulating immune reactions and the influence of immune checkpoint inhibitors on autoimmunity development.
Keyphrases
  • immune response
  • multiple sclerosis
  • dendritic cells
  • toll like receptor
  • drug induced
  • escherichia coli
  • staphylococcus aureus
  • pseudomonas aeruginosa
  • free survival
  • genetic diversity