Composition for preventing or treating sepsis or septic shock comprising adk protein as active ingredient
a technology for sepsis or septic shock and active ingredients, which is applied in the direction of peptide/protein ingredients, antibacterial agents, transferases, etc., can solve the problems of sepsis, severe disease, and infection throughout the whole body, and achieve excellent therapeutic effects, inhibit binding effect, and enhance viability
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example 1
Isolation of Dendritic Cells and Cloning of Recombinant ADK
[0043]1.1 Isolation and Induction of Dendritic Cells
[0044]Femoral bone marrow was extracted from 6- to 8-week old C57BL / 6 mice using a syringe configured to extract a bone marrow. The extracted bone marrow was washed, and red blood cells were then removed with ammonium chloride. The isolated cells were cultured at 37° C. for 8 days under a 5% CO2 atmosphere in a 6-well plate whose wells contained an RPMI 1640 medium (supplemented with 10% fetal bovine serum (FBS), 2 mM L-glutamine, 100 U / ml penicillin / streptomycin, 50 μM mercaptoethanol, 0.1 mM non-essential amino acids, 1 mM sodium pyruvate, 20 ng / ml GM-CSF, and 20 ng / ml IL-4). GM-CSF and IL-4 were used to induce differentiation of the cells into dendritic cells.
[0045]1.2 Cloning of Recombinant ADK (Rv0733)
[0046]An ADK (Rv0733) region was amplified by a polymerase chain reaction (PCR) using the genomic DNA of Mycobacterium tuberculosis as a template (primers: 5′-CATATGAGAGT...
example 2
Analysis of Expression of Surface Molecules by ADK in Dendritic Cells
[0047]To determine an effect of ADK on expression of surface molecules in dendritic cells, this experiment was performed, as follows. Dendritic cells were treated respectively with ADK at concentrations of 1, 5 or 10 μg / ml or LPS at concentrations of 50 ng / ml for 24 hours, and then recovered. LPS was a substance known to promote the maturation of dendritic cells. To analyze the expression of the surface molecules in the dendritic cells, the dendritic cells were stained with cell surface molecule-specific antibodies such as anti-CD11c-FITC, anti-CD80-PE, anti-CD86-PE, anti-MHC I-PE, and anti-MHC II-PE antibodies for 30 minutes, and then washed with PBS. The stained dendritic cells were fixed in 4% paraformaldehyde, and analyzed using a flow cytometer FACSCalibur (Becton Dickinson, San Jose, Calif.). The results are shown in FIG. 2. As shown in FIG. 2, it was revealed that, when the dendritic cells were treated with ...
example 3
Analysis of Effect of ADK on Secretion of Cytokines in Dendritic Cells
[0048]To determine an effect of ADK on secretion of cytokines in dendritic cells, this experiment was performed, as follows. The dendritic cells were pre-treated with ADK at a concentration of 1, 5 or 10 μg / ml for an hour, treated with LPS at a concentration of 50 ng / ml for 24 hours, and the culture broth was recovered. Thereafter, the secretion levels of cytokines (TNF-α, IL-6, IL-1β, and IL-12 p70) were measured from the recovered culture broth using ELISA. The results are shown in FIG. 3.
[0049]As shown in FIG. 3, it was revealed that the secretion of the cytokines increased by LPS was reduced with an increasing concentration of ADK used for pretreatment of the dendritic cells.
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