A kind of 2019-ncov subunit vaccine composition and its immunization method

A 2019-ncov, subunit vaccine technology, applied in biochemical equipment and methods, microorganisms, pharmaceutical formulations, etc., can solve problems that have not yet been raised, and achieve the effects of improving immune resistance, inhibiting invasion, and improving efficiency

Active Publication Date: 2021-09-03
陈宛莎
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0009] To the best of our knowledge, no intranasal administration of a coronavirus capsid subunit vaccine has been proposed so far, which would be an effective means of conferring protection against infection

Method used

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  • A kind of 2019-ncov subunit vaccine composition and its immunization method
  • A kind of 2019-ncov subunit vaccine composition and its immunization method
  • A kind of 2019-ncov subunit vaccine composition and its immunization method

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0085] Example 1 Computer simulation specific process of S glycoprotein binding to human ACE2 receptor

[0086] The 2019-nCoV virus S glycoprotein is a precursor protein consisting of approximately 1,300 amino acids, which can be cleaved into an amino (N)-terminal receptor-binding subunit S1 (approximately 700 amino acids) and a carboxy (C)-terminal Fusion subunit S2 (about 600 amino acids). The S1 subunit contains the receptor ACE2-binding domain (RBD), and the S2 subunit contains a hydrophobic fusion peptide and two heptad repeat regions. The 2019-nCoV glycoprotein has two distinct protease cleavage sites: the S1 / S2 cleavage site is located between residues 660-675 of the precursor protein, while the S2' cleavage site is on the S2 subunit. Therefore, the key site that interferes with the binding of the S1 subunit of 2019-nCoV to the human ACE2 receptor is before residues 660-675.

[0087] We report the computer simulation structure of the 2019-nCoV glycoprotein binding to ...

Embodiment 2

[0093] The preparation of embodiment 2 gel emulsifier

[0094] Weigh 3.0 g of dipalmitoylphosphatidylcholine into a 50 mL beaker, add 1.2 g of oleic acid and mix together to form a uniform paste.

[0095] Add 0.72 g of arginine to 30 mL of distilled deionized water and add it to dipalmitoylphosphatidylcholine oleic acid paste and heat to 45 °C. Mixed by magnetic stirring, the mixture forms a transparent and stable gel. Store the gel.

[0096] Take 100 mL of gel, add 2 mg of synthesized and purified glycoprotein, stir magnetically for 3 minutes, shake in an ultrasonic water bath for 15 minutes, dispense into vials of 20 μg per mL, for 1 person, and store in a refrigerator at 4°C.

Embodiment 3

[0097] The preparation of embodiment 3 liposomes

[0098] 120 g dipalmitoylphosphatidylcholine and 24 g oleic acid were added together and mixed well until a white homogeneous paste was observed.

[0099] Then 2 mg of arginine was dissolved in 60 mL of phosphate-buffered saline (ionic strength = 0.15, pH = 7.4).

[0100] The arginine salt solution was added to the paste and heated to 40°C for 1 hour, or until a slightly cloudy solution was observed.

[0101] Take 100 mL of liposome suspension, add 2 mg of synthesized and purified glycoprotein, stir magnetically for 3 minutes, shake in an ultrasonic water bath for 15 minutes, dispense into vials of 20 μg per mL, for 1 person, and store in a refrigerator at 4°C.

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Abstract

The invention belongs to the technical field of medicine, and in particular relates to a 2019‑nCoV subunit vaccine composition and an immunization method thereof. The vaccine composition provided by this application is a surface glycoprotein subunit vaccine of a fusion protein composed of one or more surface glycoprotein subunits obtained from 2019-nCoV virus strains and TAT transmembrane sequences, supplemented by non-toxic pyridine Glucopyranosyl lipid is used as an adjuvant, coated with liposomes or exosomes, which has the advantages of high antigen presentation efficiency and no toxic or irritating effects on the human body.

Description

technical field [0001] The invention belongs to the technical field of drugs and vaccine compositions, and in particular relates to a 2019-nCoV subunit vaccine composition and an immunization method thereof. Background technique [0002] Coronaviruses belong to the genus Coronaviridae of the Coronaviridae family and are a class of large, enveloped, positive-strand RNA viruses. The genome size of coronaviruses is about 27 to 32 kilobases, the longest among known RNA viruses. Coronaviruses mainly infect the upper respiratory tract or gastrointestinal tract of mammals and birds, and can cause diseases of the upper respiratory tract, gastrointestinal tract and central nervous system in humans and other animals. Commonly found in livestock and domestic pets, coronaviruses can cause severe infectious disease and pose a threat to agriculture. For example, avian infectious bronchitis virus (IBV) mainly causes respiratory disease in chickens and seriously affects the poultry indust...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61K39/215A61P31/14
CPCA61K39/12A61K2039/54A61K2039/543A61K2039/55572A61P31/14C12N2770/20034
Inventor 陈宛莎
Owner 陈宛莎
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