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Biomedical subjects

M Oliver

Publications and source records attributed to M Oliver.

At least 109 records · Page 6Linked to original sources

Defective generation of tetanus-specific antibody-producing B cells after in vivo immunization of Crohn's disease and ulcerative colitis patients.

In vivo booster immunization with tetanus toxoid normally results in the temporal development of circulating populations of B cells that secrete antibody after in vitro culture. In assessing the humoral immunoregulatory status in patients with inflammatory bowel disease, we found that the antibody production by the B cells that spontaneously secrete tetanus-specific immunoglobulin G in vitro, and which occur in the circulation 7 days postimmunization, was highly variable and below normal in the majority of Crohn's disease and ulcerative colitis patients. The decreased in vitro antibody responses correlated with the lack of an increase in the serum antitetanus immunoglobulin G titers, but did not correlate with disease activity, location, or steroid therapy. The majority of patients who did not produce an immunoglobulin G-antitetanus toxoid antibody response similarly failed to produce an immunoglobulin G-antidiphtheria antibody response after immunization. Lymphocytes from the patients who failed to produce normal levels of antitetanus toxoid antibody did, however, proliferate normally when stimulated by tetanus toxoid in vitro. These results suggest there are in vivo humoral immune defects in inflammatory bowel disease.

Adult↗

Ring chromosome 21: characterization of DNA sequences at sites of breakage and reunion.

We have presented studies of an unusual child with an r21 chromosome who lacks the phenotype of Down syndrome. We have sequenced the region of the breakpoint in the normal DNA fragment and have isolated the abnormal breakpoint fragment as a 7.5-kb EcoRI fragment. We have preliminary evidence localizing the breakpoint to a few hundred base pairs of 21q DNA. Since the child lacks the classical phenotype of Down syndrome, further studies of the DNA distal to the breakpoint on the long arm of chromosome 21 may help us to elucidate "genes" important to the phenotype of Down syndrome.

Base Sequence↗

Limited choroidal hemorrhage associated with intracapsular cataract extraction.

In a prospective study, limited choroidal hemorrhage (LCH) was found in 16 of 521 eyes (3.07%) subjected to cataract extraction. It developed in ten of 69 highly myopic eyes (14.49%), three of 64 moderately myopic eyes (4.49%), and three of 388 eyes without clinically significant myopia (0.77%). A positive correlation was found between LCH and vitreous loss in myopic eyes. A cause and effect relationship was not established. Of systemic factors investigated, an association was found between LCH and cardiovascular disease (14 of 16 cases). The ophthalmoscopic appearance and clinical findings support the hypothesis that LCH and expulsive choroidal hemorrhage are manifestations of the same disease processes and share common pathophysiologic mechanisms. The cause in any one case is probably multifactorial.

Aged↗

Congenital glaucoma and incomplete congenital glaucoma in two siblings.

The case histories and eye findings of 2 siblings of a non-sanguinous marriage are reported. The first child, a girl, had the typical findings of a unilateral congenital glaucoma. Her brother had an enlarged unilateral cornea (13 mm) without Descemet breaks, and normal intraocular pressure on repeated follow-up examination over 4 years. Gonioscopy showed numerous iris processes covering the iridocorneal angle. Fundus examination revealed a cup-disc ratio of 0.4 in the affected eye and 0.1 in the normal eye. Patients whose clinical picture resembles that of our second patient should be classified as having incomplete or abortive congenital glaucoma; such patients may develop raised intraocular pressure at a later stage. The term megalocornea should be reserved for eyes with enlarged cornea, normal intraocular pressure, normal iridocorneal angles, no cup-disc asymmetry and no family history of congenital glaucoma.

Cornea↗

Ocular findings in the acquired immunodeficiency syndrome.

A patient with acquired immunodeficiency syndrome is described. Both retinae were severely affected. Vision was reduced to light perception with projection incerta in the right eye and finger counting at 1.5 m in the left eye. Eye involvement is common in this syndrome, appearing at an early stage of the disease. The fundal appearance could thus be of help in diagnosis.

Acquired Immunodeficiency Syndrome↗

Prophylactic laser photocoagulation in hereditary snowflake vitreoretinal degeneration. A family report.

Examination of 37 members of a family revealed that 17 had snowflake vitreoretinal degeneration. All those affected showed some evidence of vitreous degeneration and 13 had retinal changes with differing degrees of severity. Vitreal changes may thus present as an early stage when hardly any retinal pathology is apparent. Peripheral retinal neovascularization was seen in four patients. Rhegmatogenous retinal detachment developed in two eyes and retinal breaks in six additional eyes. Because of the poor surgical prognosis in such cases, prophylactic treatment with argon laser photocoagulation is recommended for any type of retinal break.

Adolescent↗

Shallow anterior chamber and uveal effusion after nonperforating trauma to the eye.

Three patients (a 51-year-old man, an 8-year-old boy, and a 70-year-old man) developed shallowing of the anterior chamber and uveal effusion after blunt ocular injuries. After treatment with antibiotics (all three patients), corticosteroids (one patient), a mydriatic-cycloplegic solution (two patients), and antiglaucoma drugs (one patient), the shallowing and uveal effusion resolved. Because resolution occurred within two weeks in all three cases, surgical intervention was unnecessary. Both hypotony, which is common after nonpenetrating ocular injuries, and shallowing of the anterior chamber, which is rare, may result from localized uveal effusion that is clinically undetectable.

Aged↗

Anterior vitrectomy for shallow anterior chamber after cataract extraction.

Pars plana anterior vitrectomy was performed in 9 patients with shallow anterior chamber after cataract extraction. Five patients had choroidal and/or ciliary body effusion (CCBE), and 4 had aphakic pupillary block (APB). Vitrectomy was performed only after medical treatment failed to restore a normal anterior chamber depth. In all patients the anterior chamber restored during surgery and remained so thereafter, although in patients with CCBE, the fundal pathology subsided days or even months later. The only surgical complication was a longstanding cystoid macular oedema in one patient. Pars plana vitrectomy would appear to have advantages over other surgical techniques, in similar circumstances.

Aged↗

Development of glutamate binding sites and their regulation by calcium in rat hippocampus.

The postnasal development of the Na-independent [3H]glutamate binding sites, which exhibit some characteristics of postsynaptic glutamate receptors, has been studied in rat hippocampal membranes. The amount of binding sites (expressed in pmol/hippocampus) represents 4% of the adult level at postnatal day (PND) 4, increases very rapidly until PND 9, and then increases at a slower rate reaching 80% of the adult value at PND 23. In contrast, the density of binding sites (expressed in pmol/mg protein) exhibits a maximum at PND 9 and slowly decreases to reach the adult value at PND 23. These changes seen to be only quantitative since the affinity (about 450nM) and Hill coefficient (about 1.0) of these binding sites remain constant throughout development. Calcium ions have been shown to markedly stimulate [3H]glutamate binding in adult hippocampal membranes. This effect appears on PND 9--10 and increases rapidly until PND 16 when it is similar to that seen in the adult rat. We also determined the minimum age at which long-term potentiation (LTP) of synaptic transmission could be detected in the CA1 field of hippocampal slice preparations following repetitive electrical stimulation of the Schaffer-commissural pathways. LTP was only rarely detected at PND 8 whereas it could be reliably obtained after PND 9. These results indicate that the postnatal development of Na-independent glutamate binding sites closely parallels synapse formation in the hippocampus, further supporting the idea that the binding sites are associated with a physiological receptor. They also show that the appearance of the stimulatory effect of calcium on glutamate binding occurs at a time when several forms of synaptic plasticity appear in the hippocampus. In particular the correlation of the development of LTP with the calcium-stimulation of glutamate binding suggests that these phenomena have similar cellular mechanisms.

Aging↗

Argon laser photocoagulation of symptomatic flap tears and retinal breaks of fellow eyes.

A series of 95 eyes (93 patients) with retinal breaks, high-risk candidates for rhegmatogenous retinal detachment, were treated prophylactically with argon laser photocoagulation (ALP). Group A comprised 74 eyes with flap symptomatic tears. In 28 of these (subgroup A (1)) the size of the tear was smaller than 1 disc diameter and greater than 1/3 disc diameter. In 46 eyes (subgroup A (2)) the size of the tear was at least 1 disc diameter but not greater than 3 disc diameters. Group B comprised 21 fellow eyes with 34 retinal breaks in patients who had retinal detachment in the other eye. One patient of subgroup A (1) developed a rhegmatogenous retinal detachment 6 days after ALP treatment. One patient of group B developed a retinal detachment after cataract extraction. This detachment was unrelated to the previously treated retinal break. In the series of group A the mean follow-up period was 27.8 months. From previously reported follow-up data it is probable that at least in the case of flap symptomatic tears our results can be considered conclusive. There were no complications related to the prophylactic treatment of dangerous retinal breaks with ALP. This form of treatment is accurate, easy to use, and comfortable for the patient. ALP would appear to be superior to xenon arc photocoagulation and cryopexy.

Argon↗