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Expansion of effector T cells associated with decreased PD-1 expression in patients with indolent B cell lymphomas and chronic lymphocytic leukemia.
Tonino, Sanne H; van de Berg, Pablo J; Yong, Si La; ten Berge, Ineke J; Kersten, Marie José; van Lier, René A W; van Oers, Marinus H; Kater, Arnon P.
Afiliação
  • Tonino SH; Department of Hematology, Academic Medical Center, Amsterdam, The Netherlands. s.h.tonino@amc.nl
Leuk Lymphoma ; 53(9): 1785-94, 2012 Sep.
Article em En | MEDLINE | ID: mdl-22397719
ABSTRACT
In patients with chronic lymphocytic leukemia (CLL), numbers of CD8 + CD45RA +/- CD27- effector T cells are expanded. We investigated whether this expansion is also present in other B cell malignancies and the possible mechanism underlying these changes. Whereas an increase in total CD4+and CD8+ T cell numbers was found only in CLL, numbers of CD4+ and CD8+ effector T cells were significantly increased in both CLL and indolent lymphoma, but not aggressive lymphoma and myeloma. Interestingly, PD-1 expression was decreased on effector T cells and inversely correlated with effector T cell numbers, suggesting a functional role for PD-1 in regulating T cell homeostasis. In vitro experiments revealed impaired up-regulation of PD-1 upon T cell activation in the presence of malignant but also healthy B cells. Our data suggest that in CLL and indolent lymphoma, the malignant B cells affect PD-1 expression on effector T cells, resulting in an expansion of these subsets.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfócitos T / Leucemia Linfocítica Crônica de Células B / Linfoma de Células B / Proliferação de Células / Receptor de Morte Celular Programada 1 Tipo de estudo: Risk_factors_studies Limite: Aged / Humans / Middle aged Idioma: En Ano de publicação: 2012 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfócitos T / Leucemia Linfocítica Crônica de Células B / Linfoma de Células B / Proliferação de Células / Receptor de Morte Celular Programada 1 Tipo de estudo: Risk_factors_studies Limite: Aged / Humans / Middle aged Idioma: En Ano de publicação: 2012 Tipo de documento: Article