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Biomedical subjects

O Abramsky

Publications and source records attributed to O Abramsky.

At least 163 records · Page 9Linked to original sources

Visual evoked potentials in experimental allergic encephalomyelitis.

We have compared the clinical signs, brain pathology and visually evoked responses (VEP) of guinea pigs with experimental allergic encephalomyelitis (EAE). Animals immunized with myelin basic protein had a milder disease, both from the clinical and histological points of views, compared to those immunized with crude white matter extract. However, VEP findings were quite similar in both groups. The VEP of the majority of animals from both groups showed changes before or at the same time that neurological signs appeared. Electrophysiological responses were usually characterized by abnormal wave shapes and prolonged latencies. Recovery of the VEP usually preceded the recovery from clinical signs. In contrast, the severity and incidence of brain tissue pathology was not correlated to either clinical signs or VEP changes. Possible explanations of the electrophysiological, clinical and histopathological changes and their time-course are discussed.

Animals↗

Alpha-fetoprotein suppresses experimental allergic encephalomyelitis.

Experimental allergic encephalomyelitis (EAE), induced in guinea pigs by immunization with myelin basic protein (MBP) or whole CNS homogenate was successfully treated, as well as partially prevented, by daily administration of fetal alpha-fetoprotein (alpha FP). alpha FP which is produced in high quantities during pregnancy can inhibit both the cell-mediated immune response to MBP and the binding of MBP antibody to the antigen in vitro. It has a non-specific immunosuppressive effect on both the cellular and humoral responses. It is suggested that the ability of alpha FP to suppress an experimental autoimmune disease, as presented in this model of EAE, indicates that clinical remissions of human autoimmune disease during pregnancy may be attributed to the effect of this natural substance.

Animals↗

Ictal hemiparesis.

2 cases of ictal hemiparesis in adults are presented. The clinical picture was recurrent transient hemiparesis with contralateral focal hemispheric discharge. The etiology in such cases seems to be a stimulation of the second somatosensory and/or the supplementary motor areas. Emphasis is placed on the fact that, while transient ischemic attacks in adults are readily diagnosed, some cases might be subject to misdiagnosis, being actually due to inhibitory fits.

Aged↗

Binding of myasthenia gravis antibodies to different acetylcholine receptor preparations.

A group of myasthenia gravis (MG) patients was studied in order to demonstrate the differential ability of acetylcholine receptor (AChR) antibodies to bind to AChRs from different sources. Four different AChR sources were used: human muscle, denervated rat muscle, normal rat muscle and the electric organ of the electric ray, Torpedo californica. We demonstrated that AchR antibodies from MG patients tested reacted best with receptors from human muscle, and least with the electric ray receptor. The patients were classified into three categories, each representing an antibody level pattern. THe most common pattern was that in which the antibody level for human AchR is highest, followed by decreasing values for AchRs of denervated rat muscle, normal rat muscle, and that of the electric organ of the electric ray. No correlation was found between the patient-specific antibody pattern and a clinical description of the MG patient.

Animals↗

Radioimmunoassay for detection of anti-oligodendrocyte antibodies.

A solid phase radioimmunoassay (RIA) for detection and quantitation of rabbit anti-oligodendrocyte antibody has been developed using bovine oligodendroglia preparation. The assay is simple, rapid, reproducible and economical. It is approximately 150 x as sensitive as immunofluorescence. Specificity has been established by using different bovine tissue antigens as substrate and absorption studies. This assay represents a potentially powerful tool for the detection and quantitation of anti-oligodendroglial antibodies and oligodendroglial antigens in serum and CSF of man and experimental animals.

Animals↗

Antiacetylcholine receptor antibody in neonatal myasthenia gravis.

Maternal titers to antiacetylcholine receptor antibody (anti-AChR Ab) were higher in two mothers with myasthenia gravis (MG) who had infants with neonatal MG than the nearly normal values in two mothers with MG who had unaffected infants. In one unaffected infant, another IgG antibody crossed the placenta, but an IgM antibody did not. In neonates there seems to be a correlation between the concentration of anti-AChR Ab and the presence and severity of the neonatal syndrome. The absence of fetal symptoms of MG and the delayed onset or worsening of some cases of neonatal MG may be due to high fetal levels of alpha-fetoprotein and its decline in concentration in infants after birth.

Acetylcholine↗

Influence of alpha-fetoprotein on the in vitro and in vivo immune response to acetylcholine receptor.

Alpha-fetoprotein (AFP) derived from amniotic fluid and both maternal and umbilical cord sera but not from hepatoma, blocks the binding of serum acetylcholine receptor (AChR) antibody from patients with myasthenia gravis (MG) and animals with experimental autoimmune MG (EAMG) to AChR preparations as measured by a radioimmunoassay. AFP also inhibits the AChR and mitogen induced in vitro proliferative response of lymphocytes obtained from animals with EAMG. Laboratory animals repeatedly injected with AFP fail to develop EAMG in response to sensitization with AChR. Animals with established EAMG show clinical improvement in response to AFP treatment. AChR antibodies are suppressed in such AFP-treated animals. AFP is present in increased amounts during pregnancy and thus could contribute to remissions during the second half of pregnancy in patients with MG. The rapid decrease in levels of AFP during the post-partum period may also be partly responsible for relapses seen during this period. AFP may also be responsible for the appearance of transitory neonatal MG only sometime after birth and in only a minority of cases.

Amniotic Fluid↗

Myasthenia gravis following viral infection.

The pathogenesis of myasthenia gravis is autoimmune, the real etiology, however, remains unknown. Virus has been suggested as an etiological agent of the disease. In this study we present 5 myasthenic patients, whose symptoms began a few weeks after a proven viral infection. The possibility of viral infection as etiology of myasthenia gravis is raised, and the mechanisms discussed.

Adolescent↗