Connective tissue disease-associated early interstitial lung disease diagnostic kit
A technology of pulmonary interstitial lesions and diagnostic kits, applied in disease diagnosis, measuring devices, instruments, etc., can solve problems such as difficult to repeat, difficult to accept by patients, difficult to accept by patients, etc., and achieve the effect of easy operation
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Embodiment 1
[0032] A real case study was conducted on 135 patients with rheumatoid arthritis (RA), and it was confirmed that matrix metalloproteinase 7 (MMP7), interferon-γ (IFN-γ) and chemotaxis in peripheral serum of patients with connective tissue disease pulmonary interstitial lesions Increased levels of factor IP-10. Detection of matrix metalloproteinase 7 (MMP7), interferon-γ (IFN-γ) and chemokine IP-10 levels in peripheral serum of patients can diagnose early pulmonary interstitial lesions in connective tissue diseases. The specific verification process is as follows:
[0033] 135 patients with rheumatoid arthritis (RA) were recruited from the Department of Rheumatology and Immunology of the First Affiliated Hospital of Xiamen University. All were in line with the 1982 American College of Rheumatology diagnostic criteria for RA. All enrolled patients underwent high-resolution lung CT (HRCT) and pulmonary function (PFTs) examinations, and statistics of clinical joint activity indi...
Embodiment 2
[0046] A diagnostic kit for early pulmonary interstitial lesions of connective tissue diseases made according to the experimental results of Example 1 above, including a first ELISA detection component for detecting peripheral serum MMP7 in patients with connective tissue diseases, and a second ELISA for detecting IFN-γ Detection components and a third ELISA detection component to detect IP-10.
[0047] The preparation method of the above-mentioned 96-well detection plate is as follows:
[0048] Coat 200ng / mL antibody on a 96-well plate at 100uL per well, the antibody diluent is PBS, incubate the 96-well plate at 37°C for 2 hours; incubate for two hours, wash the plate once, add 200uL of blocking solution to each well, Block at 37°C for 2 hours, wash the plate once after sealing, and place the plate in a drying room for later use; the composition of the blocking solution is: 1XPBS + 0.5% casein + 2% gelatin + 0.1% preservative (proclin-300).
[0049] The detection process of ...
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