Advertisement
Journal Home
Search for

Volume 35, Issue 8, Pages 653-661 (December 2009)


View previous. 3 of 15 View next.

Clinical applications of rituximab in allogeneic stem cell transplantation: Anti-tumor and immunomodulatory effects

Voravit RatanatharathornaCorresponding Author Informationemail address, Steven Pavleticb, Joseph P. Ubertia

Received 19 June 2009; received in revised form 15 July 2009; accepted 18 July 2009. published online 17 August 2009.

Summary 

Rituximab is a chimeric monoclonal antibody directed against CD20, a B-cell antigen expressed on B-cell lymphoma. It is widely used as single agent for the treatment of follicular lymphoma or in conjunction with other combination therapy as frontline or salvage therapy. Its efficiency in B-cell depletion has lead to other applications such as therapy for autoimmune diseases, GVHD and other immunologic complications in allogeneic stem cell transplantation. Clinical responses to rituximab unveiled the role of B-cells in the pathogenesis of these disorders. Attenuation of pathogenic antibody production partly explained the clinical response in patients with autoimmune disease and chronic GVHD, but other immune mechanisms might be operative as well. Expansion of regulatory T-cells (Tregs) following rituximab therapy indicated the interaction of T- and B-cells in chronic GVHD. Therefore, effort to maintain expansion of Tregs might be important for long-term control of these diseases. Other B-cell targeting strategy directing against B-cell-activating factor (BAFF) or its receptor could be considered in conjunction with rituximab. Recent CIBMTR data on reduced cumulative incidence of acute GVHD in patients who had prior rituximab also suggest the early role of B-cells in allogeneic transplantation, thus opening the opportunity for further immune modulation to prevent acute GVHD.

a Blood and Marrow Stem Cell Transplantation Program, Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, MI 48201, USA

b National Institute of Health, Bethesda, MD 20814, USA

Corresponding Author InformationCorresponding author. Tel.: +1 313 576 8785; fax: +1 313 576 8766.

PII: S0305-7372(09)00111-X

doi:10.1016/j.ctrv.2009.07.004


View previous. 3 of 15 View next.

Advertisement