Search PubMed⌕ Search

Biomedical subjects

A Tong

Publications and source records attributed to A Tong.

48 records · Page 3Linked to original sources

Characterization of a T-cell determinant defined by a monoclonal antibody (TH5.2) which is involved in the interleukin-2-producing and proliferative capabilities of T cells.

Utilizing an OKT-4-positive human T-cell lymphoma cell line as immunogen, we have produced a monoclonal antibody (MAb), designated TH5.2, which is capable of augmenting the interleukin-2 (IL-2) production and proliferation of antigen-activated T cells. TH5.2 MAb by itself is not mitogenic for T cells; the enhanced IL-2 production and proliferation requires costimulation with either antigen or mitogen. TH.2 MAb recognizes all peripheral blood T cells at varying intensities, but does not react with monocytes. Using dual-color fluorescence analysis, it was determined that TH5.2 MAb reacts at a higher intensity on Leu-3a-positive T cells compared to Leu-2a-positive cells. Sorting T cells on the basis of fluorescent intensity with TH5.2 MAb demonstrated that the T cells reacting at high TH5.2 intensity were able to respond to mitogen at a higher rate (5-10X), as well as produce higher concentrations of IL-2 in response to mitogen as compared to the low IL-2 intensity cells. Cytotoxically treating peripheral blood mononuclear cells (PBMC) with TH5.2 MAb plus complement, which resulted in an approximate 8% decrease in the total population, significantly reduced the ability of the cells to proliferate to both mitogen and antigen. Addition of recombinant IL-2 to the cultures was able to restore the proliferative capability of the cells. In further analyzing the ability of TH5.2 MAb to augment the proliferative capability of PBMC to antigen and mitogen stimulation in vitro, it was determined that TH5.2 MAb was capable of acting synergistically with antigen or mitogen in increasing the Il-2-producing capability of T cells. Taken together the data suggest that the TH5.2 determinants is involved in the proliferative capability of T cells and is functioning at the level of IL-2 synthesis and/or secretion.

Animals↗

Problems encountered in the immunoassay of alpha-foetoprotein in patients with hepatoma.

Immunoradiometric assays suffer from the phenomenon of paradoxical increase in count rate with increasing dilution of highly concentrated samples--the "hook-effect". This is particularly important for alpha-foetoprotein where in hepatoma may be thousands of times the upper limit of the range of immunoradiometric assays. Using a commercial kit method we have encountered some degree of hook effect in many patients with hepatoma. Significant hooking occurred after 1,000 to 2,000 micrograms/1 but the extent of the effect was sample dependent. Of the samples tested so far, only one patient produced a hook which extended into the standard curve counts range. This resulted in a measured values of 20 micrograms/1 (value on dilution: 100,000 micrograms/1). We recommend that this method should be used routinely in conjunction with a screening method e.g., counterimmunoelectrophoresis and that quantitation of very high values should be by radial immunodiffusion or a method with similar sensitivity.

Carcinoma, Hepatocellular↗

Myelin basic protein binding cells in active multiple sclerosis.

A sensitive, antigen-specific rosetting technique was used to enumerate blood cells that bind myelin basic protein (BP) in MS patients and controls. Sixteen of 23 MS patients in exacerbation but only 7 of 48 in remission formed elevated numbers of rosettes. Five of the latter 7 patients had recovered from an exacerbation within four months of the laboratory evaluation. Eight of 20 patients with progressive MS, all of whom had had disease for more than four years, had BP rosette-forming cells. None of the 16 normal volunteers and 1 of 8 neurological controls had BP rosette-forming cells. These results suggest that BP-binding cells in MS are confined to patients in acute exacerbation or within four months of activity, and those who have had progressive disease for at least four years.

Antigen-Antibody Reactions↗

Utilization of 14C-labelled Escherichia coli by rats.

1. Escherichia coli was grown on 14C-labelled glucose and fractions representing "whole cells", "cell contents" and "cell walls" were administered orally to rats. 2. 14C appearing as 14CO2 in the expired air and as unidentified radioactive products in urine and faeces was measured until the cumulative recovery showed little change with time. 3. All fractions were digested. The digestibility of cell walls was less than that of the other fractions. 4. There was considerable variation among individual rats.

Animals↗

Wound care. Part 3.

Explore the source record for details and available documents.

Aged↗