2020
DOI: 10.1016/j.ymthe.2019.11.020
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Genetically Engineered Cell-Derived Nanoparticles for Targeted Breast Cancer Immunotherapy

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Cited by 166 publications
(138 citation statements)
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“…For example, a new synthetic polyvalent antibody redirected exosome (SMART-EXO) was produced by using the transmembrane domain of human platelet-derived growth factor receptor to display two different types of monoclonal antibodies on the surface of an exosome. By targeting the CD3 receptor on the surface of T cells, SMART-EXOs with the breast cancer-related HER2 receptor and EGFR receptor can activate CTLs, which then exhibit highly potent and specific anti-tumor activity both in vitro and in vivo [163,164]. In addition, antigens can also be artificially transfected into exosomes.…”
Section: Exosomes: Underlying Targets For the Regulation Of Cancer Immentioning
confidence: 99%
“…For example, a new synthetic polyvalent antibody redirected exosome (SMART-EXO) was produced by using the transmembrane domain of human platelet-derived growth factor receptor to display two different types of monoclonal antibodies on the surface of an exosome. By targeting the CD3 receptor on the surface of T cells, SMART-EXOs with the breast cancer-related HER2 receptor and EGFR receptor can activate CTLs, which then exhibit highly potent and specific anti-tumor activity both in vitro and in vivo [163,164]. In addition, antigens can also be artificially transfected into exosomes.…”
Section: Exosomes: Underlying Targets For the Regulation Of Cancer Immentioning
confidence: 99%
“…A platform called synthetic multivalent antibodies retargeted exosome (SMART-Exo) was designed to redirect and activate T lymphocytes toward cancer cells. SMART-Exo displaying anti-CD3 together with anti-EGFR [174] or anti-HER2 antibodies [161] enabled simultaneous activation and redirection of T cells toward EGFR-or HER2-expressing breast cancer cells, respectively. The SMART-Exo therapy promoted antitumor immune responses both in vitro and in vivo [161,174] (Fig.…”
Section: Exosomes As Therapeutic Agents For Cancer Immunotherapymentioning
confidence: 99%
“…They also authenticated caffold-mediated delivery of miR-219/miR-338 could enhance myelin formation after spinal cord injury (SCI) which can inhibit myelin formation by a phenomenon that MBP expression was more extensive in scaffolds that incorporated miR-219/miR-338 (73). Similarly, maybe transfection of miR-219/miR-338 into synthetic multivalent antibodies retargeted exosome which can control cellular immunity (74) to enhance axonal remyelination after nerve injuries in the central nervous system (CNS) to treat epileptic depression.…”
Section: Exosomes Are Expected To Be a Nano-therapeutic Agent For Depmentioning
confidence: 89%