Your browser doesn't support javascript.
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add filters

Database
Language
Document Type
Year range
1.
International Journal of Pharmaceutical Research ; 12(2):2654-2667, 2020.
Article in English | Scopus | ID: covidwho-855058

ABSTRACT

Objective: to determine the level of blood markers of cellular Human Cluster of Differentiation 147 (CD147) by ELISA assay. Immunological system, establishing the profile in patientsSARS-CoV-2 invades host cells via a novel route: CD147-spike protein. Methods: a case-control study including 30 patients (10 female) with SARS-CoV-2 repertory disorder whose follow-up was carried out at the outpatient clinic of the intensive care unit Service at Al Hussain Hospital, southern of Iraq, Patients were divided into three subgroups based on the onset of symptoms within the first 6 days of the acute phase of disease: subgroup A, subgroup B, and C. according to the type of drugs. Main systemic subgroup. Treatment group included 60 outpatients (25 female) being submitted to follow-up at the same hospital for non-inflammatory diseases. For determined the plasmatic levels of Human Cluster of Differentiation 147 (CD147), groups of S proteins Results: To start with, in vitro antiviral tests showed Meplazumab, infliximab and Etrolizumab an foe of CD147 adapted neutralizer, essentially hindered the infections from attacking host cells in comparison to controls, patients with presented concentrations of CD147 products (determined by plasmatic levels of S protein circulating in blood. Conclusion: our results indicate the presence of molecular SARS-CoV-2 invades respiratory cells determined by assay in patients which confirm a decrease in the defense capacity of the cellular system against toxicity induced by drugs in these patients. © 2020, Advanced Scientific Research. All rights reserved.

2.
International Journal of Pharmaceutical Research ; 12:2264-2278, 2020.
Article in English | Scopus | ID: covidwho-820344

ABSTRACT

Background: Verify the differences in the values of lung function test parameters in patients with COVID19 and the control subject also to demonstrate the relationship between the inflammatory values and the respiratory function test parameters in patients. Distinguishing CD4 + / CD8 + T-lymphocyte in SARS CoV-2 disease as immune cells relative with levels of alpha-tumor necrosis factor (TNF-α) are critical to the formation of granuloma and TNF-alpha inhibitors compact on a third-line dealing alternative for COVID19 patients who do not respond to conventional treatment and usage. In responders with the acute phase of respirational tract syndrome. Objective: To assess the impacts of treatment with the utilization of Infliximab as inhibitor and anti-TNF-α on respiratory tracts, insusceptible cellular, and experimental attributes of patients. Strategies: Seventeen patients with CoV-2 SARS were assessed from conventional treatment with purification bronchial test, spirometer, and CT scan can rapidly to checks initiate infliximab usage. These examinations were rehashed three weeks after each drug dose. Results: Treatment infliximab inhibitor of cytokines storm, especially activity TNF-α, was very much endured without antagonistic techniques, aside from one patient who set up a possibly unsafe occasion with liver poisonousness. Thirteen patients were named respondents, TNF-α focus kicked with high lists, diminished CD4/CD8 proportion deviation, decline CD4+ T cells interconnecting the CD38, CD69, and CD147 initiation markers, and the quantity of monocytes, ESR, neutrophil, lymphocytes, and platelets (p ≤0.05 for each parameter). The extent of T administrative cells (T-regs), characterized by FoxP3 with CD4+/CD+8 T-cells, diminished in near responders. End: a period in three weeks of treatment in with SARS-CoV-2 patients by a dose of Infliximab brought about indications of diminished CD4+ /T-cell in the respiratory tract and diminished in count monocytosis in the respondents' pulmonary system. © 2020, Advanced Scientific Research. All rights reserved.

SELECTION OF CITATIONS
SEARCH DETAIL