Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Polypeptide for promoting generation of African swine fever virus antigen specific immune response in swine body and application thereof

一种非洲猪瘟病毒、免疫应答的技术,应用在生物医学领域,能够解决尚未见报道等问题,达到促进免疫应答、促进致敏免疫细胞增殖的效果

Active Publication Date: 2022-02-22
LANZHOU INST OF VETERINARY SCI CHINESE ACAD OF AGRI SCI
View PDF4 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

But so far, no fully effective ASFV subunit vaccine has been reported.

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
  • Polypeptide for promoting generation of African swine fever virus antigen specific immune response in swine body and application thereof
  • Polypeptide for promoting generation of African swine fever virus antigen specific immune response in swine body and application thereof
  • Polypeptide for promoting generation of African swine fever virus antigen specific immune response in swine body and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0056] Solid phase synthesis and purity detection of embodiment 1 polypeptide

[0057] The polypeptide of the present invention is as follows:

[0058] SEQ ID NO.1: SASAINFLL, AP1;

[0059] SEQ ID NO.2: RALKYYQFL, AP2;

[0060] SEQ ID NO.3: YTLLFNHHI, AP3;

[0061] SEQ ID NO.4: SPVMKWEYVDLL, AP4;

[0062] SEQ ID NO.5: YGVEQTHIWPL, AP5;

[0063] The above polypeptides were synthesized by Shanghai Sangon Biological Co., Ltd. The detection wavelength is 214nm. The purity of the final peptide purification product was >98%, and the structure was identified by ESI-MS. The identification results are shown in Figure 1~ Figure 5 ,in figure 1 is the identification chromatogram of AP1, figure 2 is the identification chromatogram of AP2, image 3 is the identification chromatogram of AP3, Figure 4 It is the identification chromatogram of AP4, and the peak time is 14.47min; Figure 5 It is the identification chromatogram of AP5, and the peak time is 12.65min. Depend on Fi...

Embodiment 2

[0064] Embodiment 2 porcine lymphocyte proliferation experiment

[0065] 1. Pigs immunized with inactivated ASFV virus.

[0066] Inactivate the virus with the ASFV popular strain (from the African swine fever regional laboratory of the Lanzhou Veterinary Research Institute of the Chinese Academy of Agricultural Sciences,) (10HID 50 ) immunized five 90-day-old male Landrace pigs, boosted the immunization once a month later, euthanized the pigs 7 days later, and took out the spleen after dissection. Unimmunized healthy pigs were used as negative control group.

[0067] 2. Preparation, culture and proliferation detection of splenocytes.

[0068] 1) Aseptically treat the collected pig spleen with 75% alcohol, wash it three times with PBS, cut the spleen into small pieces, place them in folded sterile gauze (2 layers), and place them in 5 mL of serum-containing 1640 medium Grind the spleen in a plate.

[0069] 2) Then draw the liquid into a 15ml centrifuge tube, centrifuge at 1...

Embodiment 3

[0078] Example 3 Detection of IFN-γ secretion by different subtypes of splenic lymphocytes

[0079] The pig immunization procedure and spleen cell isolation and culture are the same as in Example 2. After obtaining the dispersed splenocytes, prepare a single cell suspension with RPMI1640 complete medium at a concentration of 1×10 6 / ml. Inoculate into a 24-well plate, add 0.2 μg of the polypeptide (AP1-AP5) provided by the present invention to each well, and place in CO 2 Cultivate in the incubator for 60h. Collect the cells in each well, label the cells with porcine CD3, CD4, CD8 and IFN-γ specific antibodies respectively, then wash twice with PBS buffer containing 2% serum, and finally use the washing solution to disperse into a cell suspension, and use the flow Cytometer detection, respectively determine B lymphocytes, CD4 + T lymphocytes, CD8 + T lymphocytes, CD4 + CD8 + The levels of IFN-γ secreted by T lymphocytes and monocyte-macrophages.

[0080] For test resul...

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 provides a polypeptide for promoting generation of African swine fever virus antigen specific immune response by a swine body and application thereof, and belongs to the technical field of biological medicines. The polypeptide comprises one or more of a first polypeptide, a second polypeptide, a third polypeptide, a fourth polypeptide and a fifth polypeptide; and the amino acid sequences of the first polypeptide, the second polypeptide, the third polypeptide, the fourth polypeptide and the fifth polypeptide are respectively as shown in SEQ ID NO.1-SEQ ID NO.5. The polypeptide can significantly promote ASFV sensitization immune cell proliferation, and can promote a pig body to generate ASFV antigen specific immune response by promoting pig CD4 + T and CD8 + T lymphocytes to secrete IFN-gamma. After animals are immunized, immune response of pig bodies can be obviously promoted. The polypeptide or the polypeptide polymer obtained by polymerizing the polypeptide can be used for preparing a subunit vaccine of the African swine fever virus.

Description

[0001] This application is a divisional application with an application date of August 26, 2020, an application number of CN202010873537.4, and an invention title of "A Class of Polypeptides and Applications for Promoting African Swine Fever Virus Antigen-Specific Immune Response in Pigs". technical field [0002] The invention relates to the technical field of biomedicine, in particular to a class of polypeptides for promoting African swine fever virus antigen-specific immune response in pig bodies and applications thereof. Background technique [0003] African swine fever (African Swine fever, ASF) is an acute, hemorrhagic, severe disease caused by African swine fever virus (ASFV) infecting domestic pigs and various wild boars (such as African wild boars, European wild boars, etc.). infectious disease. African swine fever virus mainly infects immune cells such as macrophages and monocytes. After infection, ASFV escapes the host's innate and inherent immune defense system t...

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
Patent Type & Authority Applications(China)
IPC IPC(8): C07K7/06C07K7/08A61K39/39A61P37/04A61K39/12A61P31/20
CPCC07K7/06C07K7/08A61K39/39A61P37/04A61K39/12A61P31/20C12N2710/12034A61K2039/552A61K2039/55516Y02A50/30
Inventor 郑海学毛箬青孙德惠周晓丽朱昱茜张克山杨帆刘华南刘湘涛
Owner LANZHOU INST OF VETERINARY SCI CHINESE ACAD OF AGRI SCI
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products