LSNME/SW1

An experimental COVID-19 mRNA/exosome vaccine.

Phase of research

Potential treatment - pre-clinical evidence

How it helps

Vaccine

Drug status

Experimental

2
Supporting references
0
Contradictory references
0
AI-suggested references
0
Clinical trials

General information

LSNME/SW1 is an experimental COVID-19 vaccine formulation based on exosomes derived from the 293F cell line, which are loaded with mRNA encoding SARS-CoV-2 Spike protein and mRNA encoding a fusion protein of SARS-CoV-2 Nucleocapsid, Spike fragments, Membrane, and Envelope proteins and the human Lamp1 protein (Tsai et al., 2021).

 


Supporting references

Link Tested on Impact factor Notes Publication date
Exosome-mediated mRNA delivery in vivo is safe and can be used to induce SARS-CoV-2 immunity
Spike protein Envelope protein Nucleocapsid protein Membrane protein Cell-based therapy Animal model In vitro Mixed substance Extracellular vesicles
293F cells; C57BL/6J mice 5.16

mRNA-loaded in exosomes derived from 293F cells were injected intramuscularly in mice. The formulation elicited humoral and cellular (CD4+ and CD8+) immune responses to both Spike and Nucleocapsid proteins. The Spike-reactive T-cell response was Th-1 biased. The formulation was not toxic and did not induce adverse reactions in mice.

Oct/01/2021
Exosome-mediated mRNA delivery in vivo is safe and can be used to induce SARS-CoV-2 immunity
Spike protein RNA Envelope protein Nucleocapsid protein Membrane protein Cell-based therapy Animal model In vitro Mixed substance Extracellular vesicles
293F cells; C57BL/6J mice 5.16

mRNA-loaded in exosomes derived from 293F cells were injected intramuscularly in mice. The formulation elicited humoral and cellular (CD4+ and CD8+) immune responses to both Spike and Nucleocapsid proteins. The Spike-reactive T-cell response was Th-1 biased. The formulation was not toxic and did not induce adverse reactions in mice. 

Oct/01/2021