Your browser doesn't support javascript.
loading
Transient lymphocyte decrease due to adhesion and migration following catumaxomab (anti-EpCAM x anti-CD3) treatment in vivo
Dettmar, K; Seitz-Merwald, I; Lindemann, C; Schroeder, P; Seimetz, D; Atz, J.
Afiliación
  • Dettmar, K; Fresenius Biotech GmbH. Munich. Germany
  • Seitz-Merwald, I; Fresenius Biotech GmbH. Munich. Germany
  • Lindemann, C; EUFETS GmbH. Germany
  • Schroeder, P; EUFETS GmbH. Germany
  • Seimetz, D; Fresenius Biotech GmbH. Munich. Germany
  • Atz, J; Fresenius Biotech GmbH. Munich. Germany
Clin. transl. oncol. (Print) ; 14(5): 376-381, mayo 2012. ilus, tab
Artículo en Inglés | IBECS | ID: ibc-126912
Biblioteca responsable: ES1.1
Ubicación: BNCS
ABSTRACT

INTRODUCTION:

In patients, a transient decrease in peripheral blood lymphocyte counts was observed following intraperitoneal administration of the trifunctional monoclonal antibody catumaxomab (anti-human EpCAM x anti-human CD3). The aim of this study was to clarify the observed effect in a preclinical mouse model and to analyse the related mechanism of action in vitro. MATERIALS AND

METHODS:

A related antibody, BiLu (antihuman EpCAM x anti-mouse CD3), was administered to mice and blood leukocytes were analysed. In vitro studies measured activation and cytokine secretion from human peripheral blood mononuclear cells (PBMC). For the analysis of T cell adhesion, PBMC were preincubated with catumaxomab and then co-cultured with human endothelial cells (HUVEC); T cell adhesion was assessed in the presence or absence of endothelial cell preactivation by TNFα. Adherent T cells were determined by flow cytometry.

RESULTS:

Treatment of mice with BiLu resulted in a dosedependent transient decrease in CD3+ T cells (both CD4+ and CD8+) that returned to the normal range within 48 h. Catumaxomab physiologically activated T cells in vitro (increased CD69 expression) and induced cytokine release (TNFα, IFNγ). TNFα increased expression of adhesion molecules CD54 and CD62E on endothelial cells. Furthermore, catumaxomab dose-dependently enhanced adhesion of T cells to endothelial cells. Adhesion was further increased when endothelial cells were preactivated with TNFα.

CONCLUSIONS:

Catumaxomab increases adhesion of T cells to endothelial cells due to antibody-mediated activation of T cells and production of T cell cytokines that up-regulate endothelial cell adhesion molecules. These results provide a mechanistic rationale for the transient, reversible decrease in lymphocyte counts observed following catumaxomab administration in patients, which is likely to be due to redistribution of lymphocytes (AU)
Asunto(s)
Buscar en Google
Colección: Bases de datos nacionales / España Base de datos: IBECS Asunto principal: Miembro 7 de la Superfamilia de Receptores de Factores de Necrosis Tumoral Tipo de estudio: Estudio pronóstico Límite: Animales Idioma: Inglés Revista: Clin. transl. oncol. (Print) Año: 2012 Tipo del documento: Artículo Institución/País de afiliación: EUFETS GmbH/Germany / Fresenius Biotech GmbH/Germany
Buscar en Google
Colección: Bases de datos nacionales / España Base de datos: IBECS Asunto principal: Miembro 7 de la Superfamilia de Receptores de Factores de Necrosis Tumoral Tipo de estudio: Estudio pronóstico Límite: Animales Idioma: Inglés Revista: Clin. transl. oncol. (Print) Año: 2012 Tipo del documento: Artículo Institución/País de afiliación: EUFETS GmbH/Germany / Fresenius Biotech GmbH/Germany
...