Literature DB >> 12952218

Monocyte-derived dendritic cells in chronic lymphocytic leukemia.

Françoise Vuillier1, Guillaume Dighiero.   

Abstract

Chronic lymphocytic leukemia (CLL) results from the accumulation of small mature, slowly dividing, monoclonal B lymphocytes. The clinical course of this disease is heterogeneous, with some patients progressing rapidly with early death whilst others exhibit a more stable, possibly, non-progressing disease lasting many years. Despite progress in therapy, relapse invariably occurs and the disease remains incurable. The clinical management of CLL is therefore challenging and considerable effort has been directed towards novel therapeutic strategies aimed at reducing the disease relapse rate. Recent insights into the role of dendritic cells as the pivotal antigen-presenting cells that initiate immune responses may provide the basis for generating more effective antitumor immune responses. Consequently, dendritic cells constitute an attractive approach in the context of CLL. However, understanding the relation between dendritic cells and the cellular immune response is crucial to elucidation of how to manipulate immune responses. After summarizing general properties of dendritic cells, this review focus on the approaches exploiting monocyte-derived dendritic cells in CLL, which should help design of novel treatment strategies in this disease.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12952218     DOI: 10.1080/1042819031000079087

Source DB:  PubMed          Journal:  Leuk Lymphoma        ISSN: 1026-8022


  2 in total

1.  Dendritic cells from chronic lymphocytic leukemia patients are normal regardless of Ig V gene mutation status.

Authors:  Davorka Messmer; Gloria Telusma; Tarun Wasil; Bradley T Messmer; Steven Allen; Kanti R Rai; Nicholas Chiorazzi
Journal:  Mol Med       Date:  2004 Jul-Dec       Impact factor: 6.354

2.  Type 1-polarized dendritic cells loaded with autologous tumor are a potent immunogen against chronic lymphocytic leukemia.

Authors:  Je-Jung Lee; Kenneth A Foon; Robbie B Mailliard; Ravikumar Muthuswamy; Pawel Kalinski
Journal:  J Leukoc Biol       Date:  2008-04-21       Impact factor: 6.011

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.