A class of peptides that promote the production of African swine fever virus antigen-specific immune responses in pigs and their applications
An African swine fever virus and immune response technology, applied in the field of biomedicine, can solve problems that have not been reported yet, and achieve the effect of promoting immune response and promoting the proliferation of sensitized immune cells
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Embodiment 1
[0055] Solid phase synthesis and purity detection of embodiment 1 polypeptide
[0056] The polypeptide of the present invention is as follows:
[0057] SEQ ID NO.1: SASAINFLL, AP1;
[0058] SEQ ID NO.2: RALKYYQFL, AP2;
[0059] SEQ ID NO.3: YTLLFNHHI, AP3;
[0060] SEQ ID NO.4: SPVMKWEYVDLL, AP4;
[0061] SEQ ID NO.5: YGVEQTHIWPL, AP5;
[0062] 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. For the identification results, see Figure 1 to 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 Figur...
Embodiment 2
[0063] Embodiment 2 porcine lymphocyte proliferation experiment
[0064] 1. Pigs immunized with inactivated ASFV virus.
[0065] 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.
[0066] 2. Preparation, culture and proliferation detection of splenocytes.
[0067] 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.
[0068] 2) Then draw the liquid into a 15ml centrifuge tube, centrifuge at 1...
Embodiment 3
[0077] Example 3 Detection of IFN-γ secretion by different subtypes of splenic lymphocytes
[0078] 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.
[0079] For test resul...
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