An OKT4+ T‐Cell Population with Suppressor Activity in Sézary Syndrome

This report describes a case of Sézary syndrome with the surface marker phenotype of a mature distinct T‐cell subset OKT3+. OKT4+. OKT8−. OKT17+. OKIal−(+). Functional studies indicated that the patient's peripheral blood cells showed a very low proliferative response to non‐specific milogens (...

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Veröffentlicht in:Scandinavian journal of immunology 1983-11, Vol.18 (5), p.389-398
Hauptverfasser: FARNARIER‐SEIDEL, C., KAPLANSKI, S., GOLSTEIN, M.‐M., JANCOVICI, E., SAYAG, J., DEPIEDS, R.
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Sprache:eng
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Zusammenfassung:This report describes a case of Sézary syndrome with the surface marker phenotype of a mature distinct T‐cell subset OKT3+. OKT4+. OKT8−. OKT17+. OKIal−(+). Functional studies indicated that the patient's peripheral blood cells showed a very low proliferative response to non‐specific milogens (phytohaemagglutinin. concanavalin A. pokeweed mitogen) and failed to differentiate into plasma cells in a pokeweed mitogen—immunoglobulin‐synthesis‐driven system. In coculture with normal cells the leukuemic cells were able to suppress lectin‐induced T‐cell proliferation and B‐cell differentiation in a dose‐dependent manner. Suppressor function was not radiosensitive and did not require the presence of the OKT8+ subset for expression. These Sézary cells thus represent a suppressive T‐cell subset within the OKT4+ population. This subset may well correspond to the recently described OKT4+. OKT17+ normal suppressor cells. These findings would therefore illustrate a pathological and possibly clonal expansion of a normal OKT4+ suppressor T‐ceil subset.
ISSN:0300-9475
1365-3083
DOI:10.1111/j.1365-3083.1983.tb00870.x