[Reperfusion arrhythmia after thrombolysis].
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Biomedical subjects
Publications and source records attributed to K Zeman.
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In 32 workers of Butadiene Division of the Mazovian Refining and Petrochemical Plant cellular immunity parameters were examined. The proposed parameters allowed to select those with defected immunity and monitor the effects of occupational exposure to some xenobiotics on human immune system.
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Splenectomized individuals have been reported to have many immunological abnormalities. We have studied the proliferative response of T cells in AMLR of nine children who had undergone splenectomy after trauma. T cells from splenectomized patients showed increased proliferative response in AMLR as compared with that observed in parallelly studied controls (38.480 +/- 19.700 vs 11.160 +/- 3.760 dpm). The percentage of CD4 cells was diminished in the group of splenectomized patients. We found strong correlation between AMLR and time after splenectomy (r = -0.81, p less than 0.01). Possible mechanism of elevated AMLR following splenectomy and hypotheses on generation of AMLR are discussed.
Activated polymorphonuclear leucocytes (PMNL) secrete a specific factor possessing numerous immunoregulatory properties. The rabbit IgG antibodies against this human granulocyte factor GF (anti-GF-IgG) have significantly changed the regulatory features of GF and the same antibodies alone have also exerted immunoregulatory potency when tested in vitro. Inhibition of mixed lymphocyte reaction (MLR) proliferation after GF treatment was abolished in the presence of anti-GF-IgG. GF displays a potentiating effect on interleukin-1 (IL-1) production by human monocytes in vitro. Anti-GF-IgG did not change the potentiating capacity of GF and these specific antibodies alone also enhanced IL-1 production to the same extent as GF. In peripheral blood mononuclear cell (PBMC) cytotoxicity test, the cytotoxic activity of effector cells was markedly reduced in the presence of GF. Anti-GF-IgG partially abrogated the observed suppression, although their own features indicate a strong inhibitory effect on PBMC cytotoxicity. These contradictory results are difficult to explain but they may enable us to understand the pleiotropic immunoregulatory mechanism of both GF and anti-GF-IgG. The results of the present and recently published studies support the idea that both GF and anti-GF-IgG modify T lymphocyte function at the same receptor level.
In 137 workers of the Mazovian Refining Petrochemical Plant cellular immunity parameters were examined. The following tests were performed: number of E rosette forming cells (T lymphocytes), TG and TM lymphocytes, EAC rosette forming cells (B lymphocytes), MIF generation and suppressor and cytotoxic activity of T lymphocytes. Workers of Asphalt Oxidation Division exhibited most pronounced deviations of the test parameters, as compared to controls.
Using BMA monoclonal antibodies and fluorescent microscope, percentages and absolute numbers of lymphocytes, T cell subsets and NK cells were enumerated in peripheral blood from 126 healthy men. Although absolute numbers of total lymphocytes did not differ according to age, the numbers and percentage of natural killer (NK) cells showed positive interrelationship with age. The percentage but not absolute numbers of cells reacting with BMA 030 (CD3) and BMA 040 (CD4) antibodies were significantly increased only in groups aged of 20-29 yrs and 30-39 yrs. The percentage and number helper/inducer T cells (CD4) were comparable in the four groups of subjects. These results indicate that peripheral lymphocyte populations and T cell subsets and NK cells remarkably vary in healthy men over a wide range of ages.
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Recent data have proved that PMNLs regulate the immune responses in vitro and in vivo. PMNL specific granules contain an immunoregulatory factor termed the granulocyte factor (GF). The glycogen-induced PMNL infiltration to peritoneal cavity of rats significantly diminished the local GvHR. GF, injected subcutaneously three times at a day of challenge, one and two days after, significantly diminished local GvHR as well. GF treatment before parental lymphocyte injection had no effect on the local GvHR in rats. Inactivation of GF using anti-GF IgG antibodies, abolished the inhibitory effect of PMNLs in GvHR.
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The polymorphonuclear leukocytes (PMNLs) depress mixed leukocyte reaction (MLR) in vitro. The active factor involved in inhibition was found to be localized in the specific granules of PMNL. The adherent granulocytes secreted granulocyte factor (GF) which also diminished MLR. The functional activity of GF is reflected by inhibition of responding cell proliferation exclusively during induction of MLR; moreover, GF depresses generation of the specific suppressor cells associated with MLR. The effect of GF is modified using specific antisera.
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On the basis of literary data and of their own series of 264 adult patients, who were in 1978-1982 subjected to invasive haemodynamic examination for congenital heart disease, 162 patients operated on, and 128 patients followed up for long-term periods after surgical treatment of congenital heart disease in adult age, the authors analyse the causes of late recognition of the disease, operative complications and long-term operative results. It is pointed out that a haemodynamically serious congenital heart disease is indicated for surgical correction even in adult age, and that age itself does not represent a limitation to cardiosurgical intervention. In adult age, it is necessary to anticipate a greater number of complications and a more severe post-operative course, but the long-term results are very good.
The adherence of granulocytes induces secretion of specific granule contents. The secreted proteins were termed granulocyte factors (GF). The experiments in vivo provide evidence that GF play an essential role in the stimulation of PFC in BALB/c mice immunized with SRBC when applied before challenge three times (5 micrograms per mouse), but 50 micrograms per mouse given in the same way diminishes the response. To elucidate this discrepancy, the effect of GF on the generation of suppressor cells (SC) and helper cells (HC) in vitro has been investigated. Antigen specific nonadherent SC or HC were induced in vitro using CBA mice spleen cells incubated with 100 micrograms/ml or 0.1 mg/ml of TNP-KLH, respectively, for 4 days. GF in concentrations of 0.1 to 1 microgram/ml abolish antigen specific SC generation. SC and HC activity was tested in cooperative cultures. Antigen specific SC in delayed hypersensitivity (DTH) to BCG were induced in an in vitro system as above using normal BALB/c spleen cells and 100 micrograms/ml PPD. Nonadherent suppressor cells were transferred intravenously into cyclophosphamide (CY)-treated syngeneic recipients. The recipients were immunized to BCG immediately after the cell transfer. DTH was measured by foot-pad reaction. This reaction was positive to PPD in CY treated mice immunized to BCG, while it was suppressed by the transfer of in vitro induced SC. When the SC were induced in the presence of 1 microgram/ml GF, the suppression was abrogated. The higher GF concentrations stimulated SC activities when they were measured in response to a nonrelated antigen and in specific anti-PPD response, but the HC inhibition could not be excluded.(ABSTRACT TRUNCATED AT 250 WORDS)