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W pracy przedstawiono analizę częstości występowania wirusa TT w surowicy krwi chorych z przewlekłym zapaleniem wątroby typu B, C i o nieustalonej etiologii, a także w kontrolnej grupie krwiodawców. Dodatkowo zbadano częstość infekcji TTV u chorych szczególnie narażonych na zakażenia wirusami przenoszonymi drogą parenteralną. Dokonano także, w wybranych przypadkach, analizy sekwencji nukleotydów w genomie wirusa TT.
Introduction: The scientists look for etiopatogenic factors of multiple sclerosis among viruses and bacteria. Genetic and immunologic agents are being taken into consideration. It is more than likely that there are numerous genes that take part in a development of the disease. The influence of various factors at the same time should be considered on account of possible multifactorial etiology of the disease. Aim and material: The aim of the studies was to analyse of MSRV pol, gag, env sequences, TCRB genes and karyotypes in patients with multiple sclerosis. The experimental material was peripheral blood lymphocytes from 130 MS patients and 50 healthy individuals. Methods: Classical (GTG) and molecular cytogenetic techniques (FISH) were used in the experiments. Results: 1) MSRV pol, gag and env sequences were found in both MS patients and controls. 2) The copy number of MSRV sequences was significantly greater in MS patients than in normal individuals. 3) The number of spontaneous micronuclei was significantly greater in MS patients compared to control. 4) Various chromosomal aberrations including translocations between chromosomes 7 and 14 were observed in patients with MS. 5) Translocation of constant and variable TCRB regions, deletion of constant TCRB region at 7 chromosome, duplication of constant TCRB region at chromosome 10, amplification of constant and variable TCRB regions in MS patients with aberrant chromosomes 7 and 14 were also found. Conclusions: 1) Evident difference in MSRV pol, gag and env copy number between MS patients and control suggests that MSRV may play some role in the etiology of multiple sclerosis (latent viral infection). 2) The presence of chromosome aberrations and high amount of micronuclei in MS patients shows that the instability in MS genome often occurs.
Among of the potential agents causing multiple sclerosis MSRV virus (multiple sclerosis-associated retrovirus) is often taken into consideration. Aims of the study were (1) an assessment of MSRV potential role in MS, and (2) test of genome instability in MS patients. The material was peripheral blood lymphocytes from 92 patients with MS, 12 patients with myasthenia and 20 healthy persons. The FISH studies with labeled PCR products of pol gag and env MSRV genes in nuclei, chromosomes and chromatin fi - bers were done. Classical cytogenetic techniques were introduced into karyotypes and micronuclei analyses. MSRV pol, gag and env sequences were found in both MS patients and controls. The copy number of MSRV pol sequence was signifi cantly greater in MS patients (6ñ24 copies on nucleus) than in myasthenia (4ñ5 copies) and normal individuals (3ñ6 copies). MSRV gag sequence was found in a range of 5ñ20, 4ñ5, and 2ñ4 copies in MS patients, patients with myasthenia and healthy donors, respectively. MSRV env was found in a range of 6ñ22, 4ñ5, and 2ñ4 copies in MS patients, patients with myasthenia and healthy donors, respectively. Moreover, the number of spontaneous micronuclei was signifi cantly greater in MS patients compared to control. In patients with MS diversity of chromosome aberrations was observed. In conclusion, evident difference in MSRV pol, gag and env copy number between MS patients and control suggests that MSRV may play some role in the etiology of multiple sclerosis (latent viral infection). The presence of chromosome aberrations and high amount of micronuclei in MS patients shows that the instability in MS genome often occurs. Scientifi c work has been supported by Ministry of Scientifi c Research and Information Technology funds (Grant No 2 PO5A 139 28).
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