Human rotavirus vaccine and preparation method thereof

A rotavirus and vaccine technology, applied in the field of vaccines, can solve problems such as easy to produce immune tolerance, difficult to enhance immunity, and unable to effectively activate the complement system

Active Publication Date: 2015-01-07
BRAVOVAX +1
View PDF8 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

But this kind of polysaccharide vaccine has the following problems: (1) in young animals or infants, only weak immune response can be produced, or even no immune response, and the immune response will increase with age; (2) produce low-affinity antibodies (3) only produce short-lived immune response, do not have immune memory and immune enhancement effect during repeated vaccination; (4) easy to produce immune tolerance; (5) common adjuvant is not easy to play the role of immune enhancement to this antigen Effect, the 23-valent polysaccharide vaccine has a protection rate of 50-70% for invasive pulmonary chain infection, and can only be used for vaccination of people over 2 years old, while the peak age of onset of pneumonia is 6-12 months old; (6) has Polysaccharides with repeating structures are T cell-independent type 2 immunogens. Without the participation of T cells, they cannot induce immune memory effects, and the antibodies that stimulate the body are mainly IgM and IgG2, which cannot effectively activate the complement system
[0021] However, the above-mentioned traditional polysaccha

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Human rotavirus vaccine and preparation method thereof
  • Human rotavirus vaccine and preparation method thereof
  • Human rotavirus vaccine and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0109] 1. Preparation of magnetic nanospheres

[0110] 1. Take 2.24g FeSO 4 -7H 2 O and 3.24 g FeCl 3 -6H 2 O dissolved in 10 mL and 15 mL of dddH 2 In O, mix well after dissolving, add 100mL of dddH filtered to remove oxygen 2 O;

[0111] 2. In N 2 Stir for 5 minutes under the protection of the solution, add 50mL1mol / L NaOH solution at one time, adjust the pH of the solution to 9-10, increase the stirring speed to 200-250r / min, and continue stirring for 30min;

[0112] 3. Transfer the reaction vessel to a 65-70°C water bath and continue to 2 Stirring and aging under the protection of 30min;

[0113] 4. After the reaction, set the volume to 100mL, and observe the synthesis of magnetic particles under a microscope;

[0114] 5. Dissolve 400mgPLGA in 10mLEA solvent as the oil phase (O), add 3mL of the above magnetic particle solution as the inner water phase (W 1 ), using an ultrasonic cell breaker (120W, 60s) to carry out colostrum in an ice-water bath to prepare colos...

Embodiment 2

[0165] The difference between this example and Example 1 is that the carrier protein of the human rotavirus vaccine is rotavirus carrier protein and tetanus toxoid carrier protein.

[0166] The composition analysis results of the prepared human rotavirus vaccine are consistent with the results obtained in Example 1 within the range of theoretical error.

Embodiment 3

[0168] The difference between this example and Example 1 is that the carrier protein of the human rotavirus vaccine is rotavirus carrier protein and Haemophilus influenzae surface protein HiD.

[0169] The composition analysis results of the prepared human rotavirus vaccine are consistent with the results obtained in Example 1 within the range of theoretical error.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention discloses a human rotavirus vaccine. The human rotavirus vaccine is a combined vaccine which is formed by polyvalent pneumococcal polysaccharide and two or more than two of carrier proteins by virtue of connectors, wherein the connectors are magnetic nano-microspheres; one of the carrier proteins is a rotavirus protein. A preparation method of the human rotavirus vaccine comprises a step of respectively coupling the polyvalent pneumococcal polysaccharide and two or more than two of carrier proteins (one of the carrier proteins is the rotavirus protein) with the magnetic nano-microspheres. The human rotavirus vaccine is simple in preparation process; by adopting the human rotavirus vaccine using the nano-microspheres as the connector, the mice Th1-type immune response, and the immune persistence, specificity and affinity of the polysaccharide specific antibody can be increased; in addition, the mice can be induced so as to produce rotavirus antibodies; the human rotavirus vaccine has the prevention effect of two vaccines; therefore, the human rotavirus vaccine has very wide application prospect.

Description

technical field [0001] The invention relates to a vaccine, in particular to a human rotavirus vaccine and a preparation method thereof, belonging to the field of biotechnology. Background technique [0002] 1. The harm of microorganisms to the human body and countermeasures [0003] Microorganisms usually refer to those biological groups whose individual volume diameter is generally less than 1mm. They have a simple structure, most of which are single cells, and some do not even have a cell structure. To clarify their morphology and structure; Among them, pathogenic microorganisms refer to pathogenic microorganisms that can cause diseases of humans, animals and plants. The pathogenicity of a pathogen depends on its ability to invade the host and reproduce in vivo and resist host resistance without being eliminated by it. The pathogenicity of microorganisms has species characteristics, and the degree of pathogenicity is called virulence. The establishment of infectious dis...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
IPC IPC(8): A61K39/385A61K39/39A61K39/295A61K47/48A61P31/14A61P31/04A61K39/15
CPCA61K39/092A61K39/385A61K2039/55505A61K2039/57A61K2039/6037A61K2039/6068A61K2039/6075A61K2039/627A61K2039/70
Inventor 李东鲍路伟史晋吴克
Owner BRAVOVAX
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products