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The experiments were carried out on mice (Balb/c, 6 weeks old) exposed to restraint stress. Animals were restrained for 12 h per day at nighttime and released at daytime for 2 consecutive days. Some mice were immunized i.p. immediately before the stress with 4xl08 sheep red blood cell (SRBC). Sodium diethyldithiocarbamate (DTC, 20 mg/kg) was administered i.p. twice e.g. 4 and 2 days prior to restraint stress. Calf thymus extract (TFX, 10 mg/kg) was injected i.p. four times at 24 h intervals prior to exposure to stress. It was found that restraint stress led to thymic atrophy which was reflected in the decreased total number of thymocytes, weight index of the thymus, and caused depletion of thymocytes. In addition, it was found that restraint stress reduced humoral response to SRBC which was reflected in the decreased number of splenocytes producing anti-SRBC antibodies (PFC) and serum haemagglutynin titres (19S+7S and 7S). The total number of spleen cells and weight index of the spleen in stressed mice were also diminished. The suppressing effect of stress was observed for 10 days. Pretreatment with DTC or TFX partially counteracted the immunosuppresive effects of restraint stress. Administration of DTC or TFX retarded the stress-induced thymic atrophy and promoted the restoration of the synthesis of anti-SRBC haemagglutinins and the number of PFC. Regeneration of the thymus gland occured more rapidly in stressed mice previously treated with TFX. On the other hand, the stronger effect of restoring the humoral response to SRBC was observed for DTC.
The aim of the work was to compare selected nonspecific immunological parameters in silver and polar foxes. It was found that out of three mitogens (Con A, La and PWM) only Con A stimulated the strongest lymphocyte proliferation in both species of foxes. Mean stimulation indices and the absolute values of incorporated thymidine were significantly higher in polar foxes. The average percentages of phagocytes and the fatal indices of neutrophils were comparable in both species of foxes, while the mean value of the phagocyte index was much higher in the silver fox. However, in polar foxes a higher concentration of lysozyme in the blood serum was found. The differences in the parameters may influence the susceptibility of these foxes to some infections already at the level of nonspecific primary response.
The aim of the study was to observe the time course of the immune response in pigeons after immunization with a live (attenuated) vaccine, Zoosal T, and an autogenous bacterin (inactivated vaccine). The tube agglutination test and the ELISA test were used to measure the dynamics of serum antibodies to Salmonella, determine the white blood cell (WBC) count, and evaluate the leukogram of immunized pigeons. In order to evaluate the cellular response in immunized birds, a leukocyte migration inhibition (LMI) procedure was developed and tested. Histological changes were determined in pigeons immunized with ZOOSAL T and the experimental vaccine. The tests revealed a relationship between the beginning of the immune response as evaluated by tube agglutination and ELISA tests and by the MIF test. After immunization with ZOOSAL T, when the cellular response, as measured by the LMI test, appeared at day 14 and amounted to 32% migration inhibition, there was also a significant increase in antibody titers in the agglutination test (70.00) and an increase in ELISA OD values (0.259). After a single administration of the experimental vaccine, the agglutination antibody titers at day 21 of the experiment increased markedly (93.33), as did ELISA OD value, which increased until day 35 (to 0.345). Leukocyte migration inhibition reached the highest value (26%) at day 28, which shows that the immune response after single immunization increased more slowly than in group B. At day 7 after repeat vaccination with the autogenous bacterin, there was a significant increase in agglutination antibody titers (320.00). Similar patterns of changes were observed in the ELISA test. High OD values appeared at day 7 after revaccination (0.985) and persisted during the subsequent days of the experiment (28 days after revaccination: OD = 0.931) The cellular response appeared as early as 24 hours after revaccination (39% migration inhibition) and increased very rapidly, reaching 76% inhibition at day 3. Subsequently, there was a slow decline, but 2 weeks after repeat vaccination, the percentage of migration inhibition was still 22% (tab. 1, 2, 5). Our study demonstrated that the experimental vaccine based on an isolated strain of Salmonella Typhimurium var. Copenhagen, containing carbomer and Ginseng extract (Radix panax ginseg), administered twice to domestic pigeons induced a humoral and cellular immune response that was twice as strong as the response induced by the commercial vaccine ZOOSAL T.
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