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10.2217/nnm-2020-0269

http://scihub22266oqcxt.onion/10.2217/nnm-2020-0269
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33252301!ä!33252301

suck abstract from ncbi


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pmid33252301      Nanomedicine+(Lond) 2020 ; 15 (29): 2883-2894
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  • Nanomedicinal delivery of stimulator of interferon genes agonists: recent advances in virus vaccination #MMPMID33252301
  • Chattopadhyay S; Hu CJ
  • Nanomedicine (Lond) 2020[Dec]; 15 (29): 2883-2894 PMID33252301show ga
  • The discovery of stimulator of interferon genes (STING) and their agonists as primary components that link antiviral innate and adaptive immunity has motivated growing research on STING agonist-mediated immunotherapy and vaccine development. To overcome the delivery challenge in shuttling highly polar STING agonists, typically in the form of cyclic dinucleotides, to target cells and to STING proteins in cellular cytosol, numerous nanoformulation strategies have been implemented for effective STING activation. While many STING-activating nanoparticles are developed to enhance anticancer immunotherapy, their adoption as vaccine adjuvant has vastly propelled antiviral vaccination efforts against challenging public health threats, including HIV, influenza and coronaviruses. In light of the COVID-19 pandemic that has thrusted vaccine development into the public spotlight, this review highlights advances in nanomedicinal STING agonist delivery with an emphasis on their applications in antiviral vaccination.
  • |*COVID-19 Drug Treatment[MESH]
  • |*Pandemics[MESH]
  • |Antiviral Agents/therapeutic use[MESH]
  • |COVID-19 Vaccines/immunology/*therapeutic use[MESH]
  • |COVID-19/pathology/virology[MESH]
  • |Humans[MESH]
  • |Immunity, Innate/*drug effects[MESH]
  • |Immunotherapy/trends[MESH]
  • |Nanoparticles/chemistry/therapeutic use[MESH]
  • |SARS-CoV-2/immunology/pathogenicity[MESH]


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