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10.1038/s41467-021-21634-1

http://scihub22266oqcxt.onion/10.1038/s41467-021-21634-1
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33649323!7921634!33649323
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suck abstract from ncbi


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pmid33649323      Nat+Commun 2021 ; 12 (1): 1346
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  • S-Trimer, a COVID-19 subunit vaccine candidate, induces protective immunity in nonhuman primates #MMPMID33649323
  • Liang JG; Su D; Song TZ; Zeng Y; Huang W; Wu J; Xu R; Luo P; Yang X; Zhang X; Luo S; Liang Y; Li X; Huang J; Wang Q; Huang X; Xu Q; Luo M; Huang A; Luo D; Zhao C; Yang F; Han JB; Zheng YT; Liang P
  • Nat Commun 2021[Mar]; 12 (1): 1346 PMID33649323show ga
  • SARS-CoV-2 is the underlying cause for the COVID-19 pandemic. Like most enveloped RNA viruses, SARS-CoV-2 uses a homotrimeric surface antigen to gain entry into host cells. Here we describe S-Trimer, a native-like trimeric subunit vaccine candidate for COVID-19 based on Trimer-Tag technology. Immunization of S-Trimer with either AS03 (oil-in-water emulsion) or CpG 1018 (TLR9 agonist) plus alum adjuvants induced high-level of neutralizing antibodies and Th1-biased cellular immune responses in animal models. Moreover, rhesus macaques immunized with adjuvanted S-Trimer were protected from SARS-CoV-2 challenge compared to vehicle controls, based on clinical observations and reduction of viral loads in lungs. Trimer-Tag may be an important platform technology for scalable production and rapid development of safe and effective subunit vaccines against current and future emerging RNA viruses.
  • |Animals[MESH]
  • |Antibodies, Neutralizing/immunology[MESH]
  • |Antibodies, Viral/immunology[MESH]
  • |Blotting, Western[MESH]
  • |COVID-19 Serotherapy[MESH]
  • |COVID-19 Vaccines/*therapeutic use[MESH]
  • |COVID-19/*immunology/*prevention & control/therapy[MESH]
  • |Enzyme-Linked Immunosorbent Assay[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Immunity, Cellular/physiology[MESH]
  • |Immunization, Passive[MESH]
  • |Immunohistochemistry[MESH]
  • |Macaca mulatta[MESH]
  • |Mice[MESH]
  • |Mice, Inbred BALB C[MESH]
  • |Microscopy, Electron[MESH]


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