z-logo
Premium
Contrasuppressor T cell leukaemia: clonal proliferation of contrasuppressor T cells in a patient with granular lymphocyte‐proliferative disorder
Author(s) -
Saito Hiroshi,
Oshimi Kazuo,
Akahoshi Masako,
Yamauchi Katsumi,
Yamada Osamu,
Mizoguchi Hideaki
Publication year - 1991
Publication title -
british journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1111/j.1365-2141.1991.tb04374.x
Subject(s) - peripheral blood mononuclear cell , cd8 , cd3 , immunology , lymphocytosis , cytotoxic t cell , biology , t lymphocyte , pokeweed mitogen , t cell , microbiology and biotechnology , antigen , immune system , in vitro , biochemistry
Summary In 12 patients with granular lymphocyte‐proliferative disorders (GLPD), we studied the capacity of patient peripheral blood mononuclear cells (PBMC) to promote or suppress polyclonal IgG synthesis by normal non‐T cells in pokeweed mitogen‐containing medium using an enzymelinked immunosorbent assay. During the experiments we found a patient whose PBMC possessed contrasuppressor function. The patient was a 27‐year‐old female with anaemia and lymphocytosis of CD3 + CD8 + granular lymphocytes (GL). Reconstitution experiments using normal donor non‐T cells and CD4 + and CD8 + T cells showed that addition of the patient's CD8 + cells abrogated the suppressor cell function of normal CD8 + T cells. The patient's PBMCs were CD3 + , CD8 + , Ia + , and Vicia villosa lectin‐adherent characteristics which are consistent with those of normal blood contrasuppressor T cells. The T cell receptor β and γ genes were found to be monoclonally rearranged. Ultrastructurally, this patient's GLs exhibited clusters of dense cytoplasmic bodies, which were not detected in the GL of other patients with GLPDs. These results indicate that the clonal proliferation of contrasuppressor T lymphocytes had occurred in this patient.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here