Publication | Open Access
Human T lymphocyte subpopulations defined by Fc receptors and monoclonal antibodies. A comparison.
422
Citations
23
References
1980
Year
Adaptive Immune SystemT-regulatory CellImmunologyImmunologic MechanismAntigen ProcessingT CellsImmune SystemImmunotherapyLymphocyte BiologyIsolated SubpopulationsRegulatory T Cell BiologyT Cell SubsetsAllergyAutoimmune DiseaseFc ReceptorsAutoimmunityT Cell ImmunityCellular Immune ResponseMonoclonal AntibodiesMedicine
Human T cell subpopulations have been defined on the basis of differential expression of either Fc receptors or specific cell-surface antigens. The study aimed to characterize T cell subpopulations bearing Fcγ and Fcμ receptors using monoclonal antibodies against T cells, monocytes, and Ia antigens. Monoclonal antibodies targeting T cells, monocytes, and Ia antigens were employed to isolate and analyze Tγ and Tμ subpopulations. The results showed that the Tμ population contained both inducer (OKT4+) and cytotoxic/suppressor (OKT5+) cells similar to unfractionated T cells, whereas the Tγ subset was largely Ia– monocytes (OKM1+) with few T lymphocytes (OKT3+), and reciprocal studies revealed that OKT4+ and OKT5+ subsets were mainly Tμ, indicating little correlation between Fc receptor–defined and monoclonal antibody–defined T cell subsets.
Human T cell subpopulations have been defined on the basis of differential expression of either Fc receptors or specific cell-surface antigens. In this study, we utilized a series of monoclonal antibodies reactive with T cells, monocytes, and Ia antigens to characterize isolated subpopulations of T cells bearing receptors for the Fc portion of IgG (T gamma) and subpopulations of T cells bearing receptors for the Fc portion of IgM T mu. The results showed that the T mu population contained both inducer (OKT4+) and cytotoxic/suppressor (OKT5+) populations and was similar to the unfractionated T cell population, whereas the T gamma subset contained few T lymphocytes (OKT3+) and was not enriched for either T cell subset defined by these monoclonal antibodies. Rather, the T gamma population was comprised largely of Ia- cells possessing a monocyte antigen (OKM1+). In reciprocal studies, it was found that both isolated OKT4+ and OKT5+ T cell subsets contained few T gamma cells, whereas both subsets were mainly comprised of T mu cells. We conclude that there is little correlation between T cell subsets defined by these monoclonal antibodies and those defined by Fc receptors.
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