Application of citric acid in preparation of medicine for preventing and/or treating autoimmune diseases
An autoimmune disease, citric acid technology, applied in the application field of medicine, can solve the problems of abnormal liver and kidney function, accompanying infection, etc., and achieve the effect of inhibiting cell differentiation, reducing the incidence rate, and reducing the score of arthritis
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Embodiment 1
[0029] Serum and urine citric acid levels are significantly reduced in patients with rheumatoid arthritis
Embodiment approach
[0031] (1) Collection of urine samples and serological samples
[0032] Serum and urine were collected from healthy controls (HC, n=36) and patients with rheumatoid arthritis (RA, n=42). In this study, 42 patients with rheumatoid arthritis who were treated at Peking University People's Hospital from March 2018 to May 2018 were consecutively included. All patients met the 1987 American College of Rheumatology classification criteria for rheumatoid arthritis or early rheumatoid arthritis. (ERA) criteria or the 2010 American College of Rheumatology / European League Against Rheumatism classification criteria for rheumatoid arthritis, and 36 sex- and age-matched healthy volunteers were included.
[0033]1) Instruct the subjects to take clean midstream urine, keep 45mL, divide into three 15mL sterile centrifuge tubes, and send them to the laboratory for storage in a -80°C refrigerator within 1 hour.
[0034] 2) On the day when the urine sample was collected, blood was collected veno...
Embodiment 2
[0044] citric acid inhibition T cells differentiate into pro-inflammatory cells Th17 and promote their differentiation into anti-inflammatory T cells Treg
[0045] method of execution
[0046] (1) Sorting T cells: separate the lymph node or spleen of the mouse, and place the lymph node in 1640 medium containing 10% fetal bovine serum, cut it into pieces with scissors, and grind it with a filter to make a single cell suspension. Spleen: Place the spleen in 1640 medium containing 10% fetal bovine serum, and grind it with a filter to make a single cell suspension. Add 6 mL of erythrocyte lysate, mix evenly by inversion, and place at room temperature for 10 min. Normal temperature, 1800rpm, centrifuge for 8min, discard the supernatant. Lymph node and spleen cells were washed twice with PBS buffer, filtered with a blue cap flow tube, and placed on ice for later use.
[0047] (2) Sorting by flow cytometry T cells (CD4+CD62L+CD44-).
[0048] (3) Coat anti-CD3 and anti-CD28 ...
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