Literature DB >> 21391897

The use of monoclonal antibodies for the treatment of graft-versus-host disease following allogeneic stem cell transplantation.

Alessandro Busca1.   

Abstract

INTRODUCTION: Graft-versus-host disease (GVHD) remains the leading cause of morbidity and mortality after allogeneic hematopoietic stem cell transplantation (HSCT). Steroids along with calcineurin inhibitors remain the standard initial therapy, however, less than half of the patients completely respond and there is no uniformly accepted therapy for patients with steroid-resistant GVHD. AREAS COVERED: This paper reviews the current role and ongoing development of mAbs in the treatment of GVHD. Various mAbs to cell surface antigens on GVHD effector cells have been investigated for the treatment of acute GVHD: these include anti-TNF-α antibodies, IL-2 receptor antagonists, anti-CD3 and anti-CD52 mAbs, while anti-CD20 mAb has been extensively investigated in the setting of chronic GVHD. Overall, response rates have been reported to be greater than 60%, although it should be emphasized that the long-term survival still remains suboptimal, mainly due to the detrimental side effects of infectious complications, progressive GVHD and relapse of underlying malignancy. EXPERT OPINION: Future challenges will include more appropriate definition of these agents in the therapeutic scenario of GVHD. Combinations of mAbs or mAb combined with newer immunosuppressive drugs might potentially achieve greater success, especially if used early in the disease process.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21391897     DOI: 10.1517/14712598.2011.566852

Source DB:  PubMed          Journal:  Expert Opin Biol Ther        ISSN: 1471-2598            Impact factor:   4.388


  7 in total

Review 1.  New and emerging therapies for acute and chronic graft versus host disease.

Authors:  LaQuisa Hill; Amin Alousi; Partow Kebriaei; Rohtesh Mehta; Katayoun Rezvani; Elizabeth Shpall
Journal:  Ther Adv Hematol       Date:  2017-11-28

Review 2.  Have we improved in preventing and treating acute graft-versus-host disease?

Authors:  Lia Perez; Claudio Anasetti; Joseph Pidala
Journal:  Curr Opin Hematol       Date:  2011-11       Impact factor: 3.284

3.  A molecular and computational diagnostic approach identifies FOXP3, ICOS, CD52 and CASP1 as the most informative biomarkers in acute graft-versus-host disease.

Authors:  Maria Cuzzola; Maurizio Fiasché; Pasquale Iacopino; Giuseppe Messina; Massimo Martino; Giuseppe Console; Roberta Fedele; Daniela Massi; Anna Grazia Recchia; Giuseppe Irrera; Fortunato Morabito
Journal:  Haematologica       Date:  2012-04-04       Impact factor: 9.941

4.  TNF-α priming enhances CD4+FoxP3+ regulatory T-cell suppressive function in murine GVHD prevention and treatment.

Authors:  Antonio Pierini; William Strober; Caitlin Moffett; Jeanette Baker; Hidekazu Nishikii; Maite Alvarez; Yuqiong Pan; Dominik Schneidawind; Everett Meyer; Robert S Negrin
Journal:  Blood       Date:  2016-06-30       Impact factor: 22.113

Review 5.  The possible diagnostic and prognostic use of systemic chemokine profiles in clinical medicine—the experience in acute myeloid leukemia from disease development and diagnosis via conventional chemotherapy to allogeneic stem cell transplantation.

Authors:  Håkon Reikvam; Hanne Fredly; Astrid Olsnes Kittang; Oystein Bruserud
Journal:  Toxins (Basel)       Date:  2013-02-18       Impact factor: 4.546

6.  In vivo depletion of lymphotoxin-alpha expressing lymphocytes inhibits xenogeneic graft-versus-host-disease.

Authors:  Eugene Y Chiang; Ganesh Kolumam; Krista M McCutcheon; Judy Young; Zhonghua Lin; Mercedesz Balazs; Jane L Grogan
Journal:  PLoS One       Date:  2012-03-12       Impact factor: 3.240

Review 7.  Advance in Targeted Immunotherapy for Graft-Versus-Host Disease.

Authors:  Lingling Zhang; Jianhua Yu; Wei Wei
Journal:  Front Immunol       Date:  2018-05-16       Impact factor: 7.561

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.