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    Journey of an mRNA Vaccine
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    Journey of an mRNA Vaccine

    6972

    The SARS-CoV-2 virus (the virus that causes COVID-19) has a spike protein that it uses like a tool to break into and infect cells. On its own, the spike protein is harmless and can be used as a tool to train your immune system to defend against the virus.

    Step 1: Scientists make copies of mRNA with instructions that tell the human body how to make only the outer spike protein of SARS-CoV-2.

    Step 2: mRNA is packaged inside tiny globules called lipid nanoparticles. Lipids (fatty acids) are used as the vehicle because they: Protect the mRNA from breaking down Help it pass through cell membranes and into the body's cells

    Step 3: The vaccine's mRNA instructions pass into muscle cells (near where a vaccine injection is given), and those muscle cells make copies of the spike protein.

    Step 4: Though the spikes are harmless, the body’s immune system recognizes them as antigens (foreign substances) and produces targeted antibodies to defend against them.

    Step 5: The body eliminates the vaccine material. Special white blood cells called memory cells "remember" the spike protein and which antibodies to make if they happen upon the spike again.

    Step 6: If SARS-CoV-2 (and its telltale spike proteins) enter a vaccinated person's body, the immune system reacts with antibodies that defend against infection more swiftly than it otherwise could if it had never seen the spike protein.

    Featured in Pathways: Vaccine Science.”
    Public NoteAn infographic showing the steps in an mRNA vaccine’s journey.
    Internal Note
    Keywords
    SourceNational Institute of General Medical Sciences.
    Date
    Credit LineNational Institute of General Medical Sciences.
    Investigator
    Record TypeIllustration
    Topic Area(s);#Chemistry, Biochemistry, and Pharmacology;#Injury and Illness;#
    Previous Uses
    StatusActive

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Low54 KB 11/7/2023 9:22 AMCrowley, Rachel (NIH/NIGMS) [E]
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Thumbnail3 KB 11/7/2023 9:22 AMCrowley, Rachel (NIH/NIGMS) [E]
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High3332 KB 11/7/2023 9:22 AMCrowley, Rachel (NIH/NIGMS) [E]

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