A detection kit for severe sepsis and acute liver failure
A sepsis, kit technology, applied in the field of immunology
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Embodiment 1
[0041] Example 1 Poor prognosis of acute severe liver failure patients with suppressed differentiation of monocyte subsets in vitro
[0042] Using the detection kit of the present invention, by detecting patient 1, male, 58 years old, his mononuclear cell differentiation ability (such as figure 1 As shown), the basic situation of the patient: the onset of the disease manifested as fatigue, poor appetite, yellow urine for 1 week, exacerbation with confusion for 1 day, no previous history of liver disease, prothrombin activity PTA was 27%, in line with acute severe liver disease Diagnostic criteria for failure. After the patient's first peripheral blood sample was collected (the first day after admission), 200 microliters of whole blood was collected and placed in a 96-well peripheral blood plate with a total of 3 wells, placed at 37°C, 5% CO 2 Incubate in the incubator of the whole blood sample, take the blood sample at 0 hours, double-stain with the flow cytometry antibody ...
Embodiment 2
[0043] Example 2 Patients with acute severe liver failure who successfully differentiated monocyte subsets in vitro have a good prognosis (survival):
[0044] Using the detection kit of the present invention, by detecting patient 2, male, 45 years old, the basic situation of the patient: the onset of the disease showed anorexia with dark urine color for 1 week, HBV was found to be positive 20 years ago, and the prothrombin activity PTA was 38%. Peripheral blood at 37°C, 5% CO 2 After incubation in the incubator for 36 hours, the component reagents in the diagnostic kit were detected and analyzed by flow cytometry, which showed that the mononuclear cells were successfully differentiated (Mo2 / Mo1 > 1). The analysis results showed that the prognosis was good, and the patient was finally treated by medical survived.
Embodiment 3
[0045] Example 3 Severe sepsis patients (liver is the first organ to fail) with poor prognosis in vitro monocyte subgroup differentiation suppression
[0046] Using the detection kit of the present invention, by detecting patient 3, male, 45 years old, his mononuclear cell differentiation ability (such as figure 2 As shown), the basic situation of the patient: the onset of anorexia accompanied by dark urine for 3 weeks, HBV positive was detected 20 years ago, and the prothrombin activity PTA was 34%. Due to liver failure, it was in line with severe sepsis blood standard. After the patient’s first peripheral blood sample was collected, 200 microliters of whole blood was taken and seeded into a 96-well peripheral blood plate, with a total of 3 wells, placed at 37°C, 5% CO 2 Incubate in the incubator of the whole blood sample, take the blood sample at 0 hours, double-stain with the flow cytometry antibody CD14 FITC and CD16 PE, and make the figure (1). During the incubation p...
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