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Proposing a Tandem And-Gate Car T Cell Targeting Glioblastoma Multiforme Publisher Pubmed



Sabahi M1, 2 ; Jabbari P3 ; Alizadeh Haghighi M1 ; Soltani S4 ; Soudi S5 ; Rahmani F2, 6 ; Rezaei N3, 7, 8
Authors
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Authors Affiliations
  1. 1. Neurosurgery Research Group (NRG), Student Reaserch Committee, Hamadan University of Medical Sciences, Hamadan, Iran
  2. 2. Neuroimaging Network (NIN), Universal Scientific Education and Research Network (USERN), Tehran, Iran
  3. 3. Network of Immunity in Infection, Malignancy and Autoimmunity (NIIMA), Universal Scientific Education and Research Network (USERN), Tehran, Iran
  4. 4. Student Reaserch Committee, Kermanshah University of Medical Sciences, Kermanshah, Iran
  5. 5. Department of Immunology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran
  6. 6. Students' Scientific Research Center, Tehran University of Medical Sciences, Tehran, Iran
  7. 7. Research Center for Immunodeficiencies, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran
  8. 8. Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran

Source: Medical Hypotheses Published:2020


Abstract

CAR T cell therapy is suggested as an effective method to treat hematological malignancies. However, high recurrence rates and in vivo toxicities have limited their widespread use. In order to reduce toxicity and improve tumor specificity, we propose a CAR T cell targeting glioblastoma multiforme utilizing the synNotch receptor pathway linked to a tandem CAR T cell. The extracellular domain of the synNotch receptor is replaced by a single chain fragment variable specific for the EGF receptor variant III (scfv-EGFRvIII), and covalently bonded to a IL-13Rα2-CD133-tandem CAR. This would produce an AND-gate CAR-T cell, which requires activation of both signals from synNotch receptor binding to EGFRvIII and then binding of the tandem CAR to either of the two IL-13Rα2 or CD133 ligands-specific antigens for glioblastoma stem cells. SynNotch receptor activation along with the 4-1BB costimulatory domain results in CAR T cell expression under the TRE promoter, culminating in a tri-specific and effective tumor stem cell recognition and elimination of glioblastoma multiforme. © 2020 Elsevier Ltd
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