Human leukocyte antigen gene detection kit for screening skin drug adverse reactions caused by salazosulfapyridine
A leukocyte antigen and detection kit technology, which is applied in biological testing, microbial measurement/inspection, material inspection products, etc., can solve problems such as unseen kit reports
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Embodiment 1
[0046] Example 1: Collection and extraction of genes
[0047] Sulfasalazine-induced DRESS patients were from Huashan Hospital Affiliated to Fudan University, Shanghai, China.
[0048] The diagnostic criteria were determined by Bocquet et al. (Bocquet, H., M.Bagot and J.C.Roujeau, Drug-induced pseudolymphoma and drug hypersensitivity syndrome (Drug Rash with Eosinophilia and Systemic Symptoms: DRESS). Semin Cutan Med Surg, 1996.15(4):p .250-7.) proposed that skin eruption, hematological abnormal changes (eosinophilia greater than 1500 / mm3 and abnormal lymphocytes) and system involvement symptoms (lymph node enlargement, diameter greater than 2cm or hepatitis transaminase More than 2 times the normal value, interstitial nephritis, interstitial pneumonia or carditis) three conditions are diagnosed as DRESS. Under the premise of informed consent, participants participated in the research of this subject, collected blood, and signed an informed consent form. All enrolled patients...
Embodiment 2
[0050] Example 2: Detection of HLA genotyping
[0051] The present invention adopts PCR-SSO method (recommended Kit-One Lambda, CA, USA) for HLA genotyping. Its principle is to amplify the polymorphic region of HLA first, carry out isotopic or non-isotopic labeling on the PCR products during the amplification process, and then design a series of oligonucleotide probes for the PCR amplification products according to the principle of base pairing and immobilize them in Finally, the PCR product was hybridized with the probe on the membrane, and autoradiography was used to judge the result according to the signal. HLA genotyping was performed according to the standard steps of the kit. (i.e. DNA samples, substrates, Taq enzymes, primers are mixed and mixed, added to the amplification plate, amplified according to the conditions in the kit instructions, and the amplified products are hybridized, stained and read). Results were analyzed by HLA Fusion software (One lambda, CA, US...
Embodiment 3
[0052] Example 3: HLA-B*13:01 is associated with DRESS caused by sulfasalazine
[0053] Statistics: SPSS16.0 was used to calculate Odds Ratio (OR) and its 95% confidence interval. If necessary, Haldane's correction was used, and chi-square test was used for statistical analysis. The statistical significance level was set at P less than 0.05.
[0054] Results: A total of 6 patients with DRESS caused by sulfasalazine were collected (Table 1), and 30 patients were in the sulfasalazine-resistant group. The positive ratio of HLA-B*13:01 in sulfasalazine-induced DRESS patients was significantly different from that in normal control group and sulfasalazine-resistant group (Table 2). HLA-B*13:01 binding model with sulfasalazine see figure 1 (Schematic diagram of the binding model of sulfasalazine to HLA-B*13:01).
[0055] Table 1. Clinical features and HLA types of DRESS induced by sulfasalazine
[0056]
[0057] Table 2. HLA-B*13:01 positive ratio of sulfasalazine-induced DRESS...
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