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CD137 and CD137L signals are main drivers of type 1, cell-mediated immune responses.
Dharmadhikari, Bhushan; Wu, Meihui; Abdullah, Nur Sharalyn; Rajendran, Sakthi; Ishak, Nur Diana; Nickles, Emily; Harfuddin, Zulkarnain; Schwarz, Herbert.
Affiliation
  • Dharmadhikari B; Department of Physiology, and Immunology Programme, National University of Singapore , Singapore.
  • Wu M; Department of Physiology, and Immunology Programme, National University of Singapore , Singapore.
  • Abdullah NS; Department of Physiology, and Immunology Programme, National University of Singapore , Singapore.
  • Rajendran S; Department of Physiology, and Immunology Programme, National University of Singapore , Singapore.
  • Ishak ND; Department of Physiology, and Immunology Programme, National University of Singapore , Singapore.
  • Nickles E; Department of Physiology, and Immunology Programme, National University of Singapore , Singapore.
  • Harfuddin Z; Department of Physiology, and Immunology Programme, National University of Singapore, Singapore; NUS Graduate School for Integrative Sciences and Engineering, National University of Singapore, Singapore.
  • Schwarz H; Department of Physiology, and Immunology Programme, National University of Singapore, Singapore; NUS Graduate School for Integrative Sciences and Engineering, National University of Singapore, Singapore.
Oncoimmunology ; 5(4): e1113367, 2016 Apr.
Article in En | MEDLINE | ID: mdl-27141396
ABSTRACT
CD137 is expressed on activated T cells and NK cells, among others, and is a potent co-stimulator of antitumor immune responses. CD137 ligand (CD137L) is expressed by antigen presenting cells (APC), and CD137L reverse signaling into APC enhances their activity. CD137-CD137L interactions as main driver of type 1, cell-mediated immune responses explains the puzzling observation that CD137 agonists which enhance antitumor immune responses also ameliorate autoimmune diseases. Upon co-stimulation by CD137, Th1 CD4+ T cells together with Tc1 CD8+ T cells and NK cells inhibit other T cell subsets, thereby promoting antitumor responses and mitigating non-type 1 auto-immune diseases.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Oncoimmunology Year: 2016 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Oncoimmunology Year: 2016 Document type: Article Affiliation country: