Abstract
The nature of Ia antigens which appear on human T cells after activation and the stimuli required for their expression was examined utilizing a monoclonal antibody reactive with the Ia antigen framework. T cells were purified using monoclonal antibodies directed either at the entire T-cell population (OKT3) or the T-cell inducer subset (OKT4). By indirect immunofluorescence, it was shown that the human T-cell population contains no detectable Ia+ cells in the resting state. In contrast, in excess of 60% of the T-cell population expresses Ia antigen after alloactivation in the mixed lymphocyte culture. Moreover, these Ia antigens are expressed within both the OKT4+ and OKT4- subsets. Similarly, phytohemagglutinin and concanavalin A induced approximately 20% of peripheral T cells to express Ia antigen and the expression of these antigens is not restricted to either OKT4 subset. In contrast, only the inducer T-cell population which proliferates maximally to soluble antigen expresses Ia antigens after activation by tetanus toxoid. Thus, the expression of human Ia antigens on unique T-cell subsets depends upon the activation stimuli utilized and ability of the individual subset to respond to a given stimulus. Additional studies indicated that Ia antigens appear on previously Ia- T cells after activation and do not result from clonal expansion of a small subset of Ia+ T cells.
MeSH Terms
Antigen-Antibody Reactions
Antigens, Surface/analysis,genetics
Clone Cells/immunology
Epitopes
Genes, MHC Class II
Humans
Lymphocyte Activation
T-Lymphocytes/immunology
Chemicals
Antigens, Surface
Epitopes
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Reinherz E L
Kung P C
Pesando J M
Ritz J
Goldstein G
Schlossman S F
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18 references, click to expand
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