T4 cell activation by immobilized phytohemagglutinin: differential capacity to induce IL-2 responsiveness and IL-2 production.
Open Access
- 15 October 1988
- journal article
- research article
- Published by Oxford University Press (OUP) in The Journal of Immunology
- Vol. 141 (8) , 2593-2600
- https://doi.org/10.4049/jimmunol.141.8.2593
Abstract
Soluble mitogens, such as PHA induce accessory cell (AC)-dependent T cell proliferation. One function of the AC is to create a stimulatory matrix. Therefore, experiments were carried out to determine whether PHA immobilized onto microtiter plates could stimulate T cells in the absence of AC. Peripheral blood T4 cells were cultured under limiting dilution conditions with either soluble or immobilized PHA with or without rIL-1 beta, rIL-2, r-TNF-alpha, an anti-CD28 mAb (9.3), or irradiated EBV-transformed B cells as AC. The frequency of proliferating T4 cells was assessed by examining wells microscopically, and the frequency of T4 cells producing IL-2 was assessed by examining the ability of supernatants to support CTLL-2 proliferation. The percentage of T4 cells growing and producing IL-2 was determined by a maximum likelihood procedure. Immobilized, but not soluble, PHA induced a mean of 20.0 +/- 2.6% of T4 cells to grow in the complete absence of AC in medium supplemented with rIL-2. Whereas rIL-1 beta, rTNF-alpha, and 9.3 were unable to support T4 cell growth in the absence of rIL-2, each enhanced the percentage of T4 cells responding to immobilized PHA in the presence of rIL-2. In contrast, both soluble and immobilized PHA were unable to induce T4 cell IL-2 production in the absence of AC, even when cultures were supplemented with rIL-1 beta or 9.3. In the presence of AC, a small percentage of T4 cells (5.4 to 11.7%) was stimulated to produce detectable amounts of IL-2 by either immobilized or soluble PHA. Moreover, in the presence of AC, a very small population (approximately 1%) of PHA-stimulated T4 cells proliferated without supplemental rIL-2. The data indicate that a matrix of immobilized PHA is sufficient for some T4 cells to be activated to respond to IL-2, whereas others require additional signals provided by rIL-1 beta, rTNF alpha, 9.3, or AC. In contrast, neither soluble nor immobilized PHA is sufficient to induce T cell IL-2 production. This response requires signals provided by intact AC.This publication has 35 references indexed in Scilit:
- The accessory cell function of human alveolar macrophages in specific T cell proliferation.The Journal of Immunology, 1984
- Phenotype of the accessory cell necessary for mitogen-stimulated T and B cell responses in human peripheral blood: delineation by its sensitivity to the lysosomotropic agent, L-leucine methyl ester.The Journal of Immunology, 1983
- Antigen presentation by human monocytes: evidence for stimulant processing and requirement for interleukin 1.The Journal of Immunology, 1983
- The accessory function of phagocytic cells in human T cell and B cell responses.The Journal of Immunology, 1982
- Phorbol ester tumor promoter modulation of alloantigen-specific T lymphocyte responses.The Journal of Immunology, 1982
- A phorbol ester (TPA) can replace macrophages in human lymphocyte cultures stimulated with a mitogen but not with an antigen.The Journal of Immunology, 1982
- Relationship of cell cycle to recovery of IL 2 activity from human mononuclear cells, human and mouse T cell lines.The Journal of Immunology, 1981
- Limiting dilution assays for the determination of immunocompetent cell frequencies. I. Data analysis.The Journal of Immunology, 1981
- Monoclonal antibodies identifying a novel T-Cell antigen and Ia antigens of human lymphocytesImmunogenetics, 1980
- "Panning" for lymphocytes: a method for cell selection.Proceedings of the National Academy of Sciences, 1978