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In terms of its anatomy and functions, the reproductive system of birds is significantly different from the one found in mammals. It consists of only the left ovary and the left oviduct, which is constantly exposed to ascending infections because of its connection with the cloaca. Hence, the proper functioning of humoral and cell-mediated local immune mechanisms in this system is very important for maintaining its physiological functions. The expression of Toll-like receptors and the presence of T and B lymphocytes have been demonstrated in both the ovary and the oviduct of chickens. CD4⁺ T cell subpopulation is distributed mainly in the lamina propria of the oviduct, whereas in the submucous membrane and muscular layer these cells are found less frequently. CD8⁺ T lymphocytes are equally distributed in all abovementioned layers of the oviduct wall. IgY⁺ B cells are distributed among the epithelial cells, and they are closely connected with the glandular tissue of the oviduct, mainly in the infundibulum, magnum, and uterus regions. IgA⁺ and IgM⁺ B cells are present in the entire oviduct, but mainly in the glandular tissue of the magnum. IgY⁺ B cells have not been detected in the ovary, unlike IgM⁺ B cells, which have been demonstrated in the ovary stroma. In addition to T and B cells, antigen-presenting cells are present in the follicle wall and in the oviduct. During the early stages of reproductive maturation, a decrease in the number of immunocompetent cells is observed in the reproductive system, and the local immnosuppression increases the susceptibility of birds to Salmonella Enteritidis infections. The number of T and B lymphocytes in the mucous membrane of the oviduct decreases with age, which facilitates infections of the reproductive system. Additionally, the local immune mechanisms of the reproductive system in birds involve the transfer of protective IgY, IgA and IgM maternal antibodies to hatching eggs. The local immune mechanisms of the reproductive tract are responsible for preventing infections that disturb the physiological functions of the reproductive system and for protecting eggs from contamination.
Dynamic and activity of myeloperoxidase and serum lysozyme, globulins, total protein in the polar blue foxes infected naturaly with the distemper virus (CDV) was examined. The two step examinations were done. In the first step the value and activity of the above mentioned parameters of unspecific humoral immunity was registered twice in 24 sick and 22 healthy foxes during sickness and just before death. In the second step the examinations were performed on 10 healthy and 12 sick foxes at the day 1, 4, 7, 10 and 13 of the disease e. g. from the appearance of the first clinical signs up to the death of the examined animals. Clinical observations, anatomopathological and virological (direct immunofluorescence test using a conjugate prepared by the Biowet Nitra, Czechoslovakia) tests were performed simultaneously with immunological tests. A complex evaluation of breeding system on 5 farms at the first step and on 3 farms at the second step of studies was also done. It was found that the natural infection of foxes with CDV increases the activity of myeloperoxidase and blood serum lysozyme and decreases the level of serum globulins.
The aim of the study was to determine the immunological state of bitches suffering from pyometra. The study was performed on 87 bitches with open pyometra, 13 bitches with closed pyometra and 17 healthy control bitches. All bitches with pyometra were treated by ovario-hysterectomy. Prior to surgery, blood samples were collected from them to determine: w.b.c., r.b.c., Hb, Ht, differential w.b.c. A NBT reduction test and phagocytic index was also performed on the blood. In addition, the lysozyme activity, total protein level and globulin fraction were evaluated in the serum. C-reactive protein (CRP) was determined in 40 of the bitches. Uterus aspirates were collected from 68 bitches with open pyometra and 13 with closed pyometra for bacteriological examination. The study demonstrated that all immunological parameters in bitches with pyometra were lower compared to those of the control group. Only the CRP level was very high. In bitches with open pyometra the following aerobes were isolated: E. coli (78%), streptococci (13%), staphylococci (6%) and Pseudomonas aeruginosa (3%). No aerobes were isolated in bitches with closed pyometra.
The aim of the study was to conduct serological examinations for the presence of humoral antibodies against CPV-2, using an ELISA test. Moreover, amplification and restriction analysis (PCR-RFLP) of the fragment at 1278 bp (VP-2 gene) strains of CPV-2 biological materials of dogs with diarrhea were performed. The studies were carried out on 377 urban dogs aged from 3 months 17 years. All animals were vaccinated with commercially available live or inactivated vaccines against canine parvovirosis at 8, 12, 16 weeks of age. Most of the dogs were revaccinated yearly. Serological examinations determined that most of the dogs had antibodies against CPV-2 (98%) at 2-3-years-of-age. The least seropositive dogs were below 5 months (89%) and above 10 years (85%). The highest mean titer CPV-2 virus antibody were found between 0.5 - 1 year. 95% animals with diarrhea were positive for canine parvovirosis by use of PCR. Moreover, the RFLP analysis of the VP-2 gene sequence enabled the distinction of 3 restriction patterns of CPV-2 circulating in the dog population. The study indicates the vaccination of dogs provides effective protection against canine parvovirosis infection. The occasional occurrence of CPV-2 in puppies and young dogs can indicate the presence of virulent strains of CPV-2 in the dog population.
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