The role of E receptors in the attachment of thymocytes and T lymphocytes to human target cells (original) (raw)

1983, Clinical immunology and …

Human thymocytes, activated T lymphocytes, and neuraminidase-treated T cells possess the distinct capacity of forming conjugates with various human cell lines. The present study investigated whether E receptors, which endow human T cells with their capacity to bind sheep red blood cells (SRBC), are involved in this phenomenon. Monoclonal antibodies to human T cells and various simple sugars were studied for their effect on the attachment of human T cells to target cells. A-22, a monoclonal antibody to the E receptor, inhibited the formation of E rosettes by T cells and SRBC, and reacted in immunofluorescent-staining assays with the majority of human thymocytes and peripheral T cells, and with T-cell lines capable of forming E rosettes. When human thymus cells were treated with A-22 antibody they showed a reduction of up to 70% in their capacity to attach to the GM-4762 lymphoblast cell line and the K-562 myeloid line. Antibody treatment of the target cells, rather than of the thymus cells, had no effect on the formation of conjugates between thymus cells and target cells. Treatment of thymus cells with various monoclonai antibodies to T cells which do not react with the E receptor had no inhibitory effect. The exposure of human thymus cells to various simple sugars (D-fWinnOSe, n-fucose, galactose, and lactose) markedly reduced their capacity of forming conjugates with target cells. Exposure of neuraminidase-treated peripheral blood lymphocytes and of activated T cells to A-22 antibody inhibited their attachment to human target cells.

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SHEEP RED CELL BINDING TO HUMAN LYMPHOCYTES TREATED WITH NEURAMINIDASE; ENHANCEMENT OF T CELL BINDING AND IDENTIFICATION OF A SUBPOPULATION OF B CELLS

Journal of Experimental Medicine, 1973

Sheep red blood cell rosette formation has been demonstrated in a number of laboratories to be a specific marker for human T cells (1-3). A variety of different methods have been utilized which have shown some differences in the percentages of T cells that form these rosettes. The procedure of Jondal and Wigzell gives values close to 100% for peripheral blood T cells and for thymocytes. Recently double labeling experiments utilizing markers for B cells along with the rosette system have indicated that independent cells are involved although rare double labeled cells may be observed (3). The simplicity and specificity of the procedure have led to wide clinical use of this method and valuable information has been obtained (3, 4).

Specific binding of antigen onto human T lymphocytes

Journal of Clinical Investigation, 1986

Human T lymphocytes sensitized to Candida aibicans (CA) were shown to proliferate in cultures induced with mannan, a ramified polysaccharide extracted from the cell well of CA. We presently describe that, when we used strongly labeled i3Hlmannan, antigen-specific T blast cells were able to bind the labeled mannan on their membrane. The observations that irrelevant blast cells did not bind I3Himannan, and that mannan-specific blast cells did not bind tritiated pneumococcal polysaccharide SiL indicate the specificity of mannan binding. Mannan binding was reversible and saturable. Mannan binding on T blast cells was inhibited by preincubation with monoclonal antibodies to T3 but not to other T cell-related molecules. The characteristics of this receptor suggest its identity with the T cell receptor for antigen. The direct binding of mannan could be either due to a cross-linking of the receptor by multivalent mannan or to a recognition of mannan in association with HLA-DQ molecules, as suggested by partial blocking of mannan binding using anti-HLA-DQ monoclonal antibodies.

A monoclonal antibody to human B lymphoblastoid cells activates human and murine T lymphocytes

Cellular immunology, 1989

A B lymphoblastoid cell line can provide a comitogenic, accessory signal for mitogen-treated T cells. In a study evaluating the antigenic determinant of such cells that mediate this effect, a monoclonal antibody (I57) was raised against the Daudi cell line. This antibody was found to interact with a 30-kDa protein on these cells and had agonistic properties. It enhanced the B lymphoblastoid accessory cell and interleukin 1 (IL-1)-dependent stimulation of PHA-treated murine thymocytes. The stimulatory effect of I57 on PHA-treated thymocytes was more pronounced at high, supraoptimal concentrations of the lectin. This was in contrast with the effect of IL-1 that failed to stimulate these cells treated with PHA at high concentrations. I57 also enhanced stimulation of thymocytes treated with IL-2 alone or with both PHA and IL-2. I57 exhibited by itself mitogenic activity for human T cells. These cells, treated with IL-2, were further stimulated by I57. I57 seems to be different from othe...

Immunoregulation of the proliferative response of lymphocytes by soluble E receptors

Clinical Immunology and Immunopathology, 1980

The role played by soluble human T-lymphocyte receptors for sheep erythrocytes (E) upon the proliferative response of lymphocytes was investigated. Preparations containing soluble E receptors, e.g., normal human serum dialysate (NHSD) and leukocyte dialysate containing transfer factor (TF) were added to cultures performed in the presence of normal human serum. In most of the cultures stimulated by allogeneic cells or by phytohemagglutinin (PHA), the addition of these preparations induced inhibition of the [3H]thymidine uptake. Previous absorption with E abolished or diminished significantly this inhibitory effect. Addition of NHSD absorbed with E restored the proliferative response in mixed leukocyte cultures performed in medium containing dialyzed normal human serum instead of NHS. The immunoregulation exerted by soluble E receptors upon the proliferative response of human lymphocytes seems to be more clearly expressed in the response to allogeneic cells than in the response to PHA.

Activation of Human T Cells by Neuraminidase-Galactose Oxidase-Treated Erythrocytes Involving CD2 (T11) and its Complementary Structure

Scandinavian Journal of Immunology, 1988

Human T lymphocyte proliferation induced by neuraminidase-galactose oxidase (NAGO)treated autologous erythrocytes (HENAGO) plus polyethylene glycol (PEG) has previously been shown to be independent of accessory cells. Here, we show that the response to HENAGO+PEG was accompanied by interleukin 2 (IL-2) release and was inhibited by anti-IL-2 and anti-IL-2 receptor antibodies, HENAGO alone initiated DNA synthesis together with phorbol ester (12-Otetradecanoyl-phorbol-13-acetate; TPA), To elucidate the nature of the stimulatory signals NAGO-treated sheep erythrocytes (SENAGO) were used in additional experiments. In parallel to the superior rosetting capacity of SE compared to HE, SENAGO were by themselves stimulatory, and the response was further enhanced by PEG or TPA, Antibody L180/1, specific for the Til (CD2) target structure (TUTS) on SE, homologous to the human CD2 ligand LFA-3, abolished the response to SENAGO alone or when combined with PEG or TPA, The results suggest that ENAGO induce T-cell response through CD2-LFA-3-T11TS interaction, and via otiier surface antigens bound by the oxidatively induced aldehyde groups on E G. Ocklind,

Cell to Cell Interaction in the Immune Response: V. Target Cells for Tolerance Induction

Journal of Experimental Medicine, 1970

Collaboration between thymus-derived lymphocytes, and nonthymus-derived antibody-forming cell precursors occurs during the immune response of mice to sheep erythrocytes (SRBC). The aim of the experiments reported here was to attempt to induce tolerance in each of the two cell populations to determine which cell type dictates the specificity of the response. Adult mice were rendered specifically tolerant to SRBC by treatment with one large dose of SRBC followed by cyclophosphamide. Attempts to restore to normal their anti-SRBC response by injecting lymphoid cells from various sources were unsuccessful. A slight increase in the response was, however, obtained in recipients of thymus or thoracic duct lymphocytes and a more substantial increase in recipients of spleen cells or of a mixture of thymus or thoracic duct cells and normal marrow or spleen cells from thymectomized donors. Thymus cells from tolerant mice were as effective as thymus cells from normal or cyclophosphamide-treated ...

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