Cell-cell interactions in the T cell proliferative response. I. Analysis of the cell types involved and evidence for nonspecific T cell recruitment.
Open Access
- 1 August 1980
- journal article
- research article
- Published by Oxford University Press (OUP) in The Journal of Immunology
- Vol. 125 (2) , 491-500
- https://doi.org/10.4049/jimmunol.125.2.491
Abstract
In the antigen-induced T cell proliferative response, it has been firmly established that antigen-specific T cell activation signals are provided by a specialized antigen-presenting cell (APC). However, the number of responding T cell populations involved has not been clearly delineated. This problem can be analyzed by plotting the logarithm of the number of cultured cells against the logarithm of the response. This yields a straight line, the slope of which indicates the minimum number of interacting cell populations that are required to give the response. In the antigen-induced T cell proliferative response, this number is 3. Based on their ability to shift the slopes of the log cell number-log response line, two of the populations were identified to be T cells. The third cell, which was present in irradiated spleens, possessed certain properties of the APC. Of the two T cells, one was antigen-specific and the other could come from normal unprimed animals. The frequency of antigen-specific proliferating T cells in primed animals was estimated to be only 1 in 1.3 x 10(3), and a large proportion of the proliferation was shown to be due to unprimed cells. Furthermore, without the need to use antigen-pulsed macrophages, this slope analysis demonstrated convincingly that the successful interaction between APCs and proliferating T lymphocytes is determined by products of the I-region immune response genes.This publication has 14 references indexed in Scilit:
- Immunoregulatory circuits among T-cell sets. Identification of a subpopulation of T-helper cells that induces feedback inhibition.The Journal of Experimental Medicine, 1978
- Antigen presentation in the murine T lymphocyte proliferative response. II. Ir‐GAT‐controlled T lymphocyte responses require antigen‐presenting cells from a high responder donorEuropean Journal of Immunology, 1978
- ADHERENT CELL-FUNCTION IN MURINE T-LYMPHOCYTE ANTIGEN RECOGNITION .1. MACROPHAGE-DEPENDENT T-CELL PROLIFERATION ASSAY IN MOUSE1978
- Initiator and recruited T lymphocytes are distinct subclasses of T lymphocytesEuropean Journal of Immunology, 1978
- Evidence for an immunoglobulin-dependent antigen-specific helper T cell.Proceedings of the National Academy of Sciences, 1977
- Antigen presentation in the murine T-lymphocyte proliferative response. I. Requirement for genetic identity at the major histocompatibility complexThe Journal of Experimental Medicine, 1977
- T-lymphocyte-enriched murine peritoneal exudate cells. IV. Genetic control of cross-stimulation at the T-cell level.The Journal of Experimental Medicine, 1977
- SUBPOPULATIONS OF LYMPHOCYTES TO PRODUCE VARIOUS LYMPHOKINES .1. FUNCTION OF SUBPOPULATIONS SEPARATED BY VELOCITY SEDIMENTATION1977
- LYMPHOCYTE SPECIFICITY TO PROTEIN ANTIGENS .1. CHARACTERIZATION OF ANTIGEN-INDUCED INVITRO T-CELL-DEPENDENT PROLIFERATIVE RESPONSE WITH LYMPH-NODE CELLS FROM PRIMED MICE1977
- Separation of helper T cells from suppressor T cells expressing different Ly components. I. Polyclonal activation: suppressor and helper activities are inherent properties of distinct T-cell subclasses.The Journal of Experimental Medicine, 1976