Literature DB >> 12939720

Monoclonal antibodies for the prevention and treatment of graft-versus-host disease.

Rebecca J Bruner1, Sherif S Farag.   

Abstract

Acute and chronic graft-versus-host disease (GvHD) remain major obstacles to successful allogeneic hematopoietic stem cell transplantation, contributing substantially to morbidity and non-relapse mortality. Better understanding of the immunopathophysiology of GvHD has identified a number of targets for intervention. Among newly developed agents suitable for the prevention and treatment of GvHD, monoclonal antibodies hold much promise. Monoclonal antibodies currently available, such as infliximab and anti-interferon-gamma (anti-IFN-gamma), are capable of blocking of the action of initiating and effector cytokines. Antibodies directed against activated T cells, including daclizumab, visilizumab and ABX-CBL, may offer more specificity than the more broadly acting pan-T-cell-depleting agents. Finally, the clinical investigation of antibodies to adhesion molecules (such as LFA-1), or distal effector mechanisms (such as FasL) may offer another level of specificity. Many of these monoclonal antibodies have already undergone clinical testing. Campath-1H has been used for the prevention of acute GvHD with success. Daclizumab, infliximab, visilizumab, and ABX-CBL have shown promising activity in steroid-resistant acute GvHD in early clinical testing. This review summarizes current experience with monoclonal antibodies in the management of acute and chronic GvHD. Over the next decade, however, the challenge will be to define the relative place of these antibodies in the therapeutic armamentarium for GvHD and their impact on long-term survival.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12939720     DOI: 10.1016/s0093-7754(03)00250-1

Source DB:  PubMed          Journal:  Semin Oncol        ISSN: 0093-7754            Impact factor:   4.929


  6 in total

1.  Diabetes, hypertension, and cardiovascular events in survivors of hematopoietic cell transplantation: a report from the bone marrow transplantation survivor study.

Authors:  K Scott Baker; Kirsten K Ness; Julia Steinberger; Andrea Carter; Liton Francisco; Linda J Burns; Charles Sklar; Stephen Forman; Daniel Weisdorf; James G Gurney; Smita Bhatia
Journal:  Blood       Date:  2006-10-17       Impact factor: 22.113

2.  Human Amniotic Mesenchymal Stem Cells Inhibit aGVHD by Regulating Balance of Treg and T Effector Cells.

Authors:  Ya Gao; Weiru Li; Xiaoyin Bu; Ying Xu; Shengchun Cai; Jinman Zhong; Meixue Du; Haitao Sun; Liping Huang; Yongjian He; Xiumei Hu; Qifa Liu; Hua Jin; Qian Wang; Baohong Ping
Journal:  J Inflamm Res       Date:  2021-08-16

3.  Addition of infliximab to standard acute graft-versus-host disease prophylaxis following allogeneic peripheral blood cell transplantation.

Authors:  Mehdi Hamadani; Craig C Hofmeister; Buffy Jansak; Gary Phillips; Patrick Elder; William Blum; Sam Penza; Thomas S Lin; Rebecca Klisovic; Guido Marcucci; Sherif S Farag; Steven M Devine
Journal:  Biol Blood Marrow Transplant       Date:  2008-07       Impact factor: 5.742

4.  Suppression of established experimental autoimmune uveitis by anti-LFA-1alpha Ab.

Authors:  Yan Ke; Deming Sun; Ping Zhang; Guomin Jiang; Henry J Kaplan; Hui Shao
Journal:  Invest Ophthalmol Vis Sci       Date:  2007-06       Impact factor: 4.799

5.  Sequential development of interleukin 2-dependent effector and regulatory T cells in response to endogenous systemic antigen.

Authors:  Birgit Knoechel; Jens Lohr; Estelle Kahn; Jeffrey A Bluestone; Abul K Abbas
Journal:  J Exp Med       Date:  2005-11-14       Impact factor: 14.307

6.  CD147 blockade as a potential and novel treatment of graft rejection.

Authors:  Jing Luan; Yu Zhao; Yang Zhang; Jinlin Miao; Jia Li; Zhi-Nan Chen; Ping Zhu
Journal:  Mol Med Rep       Date:  2017-08-09       Impact factor: 2.952

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.