Literature DB >> 20881491

New generation CD3 monoclonal antibodies: are we ready to have them back in clinical transplantation?

Sylvaine You1, Lucienne Chatenoud.   

Abstract

PURPOSE OF REVIEW: The continuing problem of late graft loss and immunosuppressive drug toxicity forces us to explore new treatments for the induction of transplant tolerance. Monoclonal antibodies targeting molecules implicated in lymphocyte activation, in particular CD3/TCR, constitute a promising strategy. RECENT
FINDINGS: Promising results were obtained from the use of antibodies targeting CD3/TCR, coreceptors or costimulatory pathways as tolerance-promoting tools in experimental transplantation. These antibodies do not uniformly depress the immune system but act in an antigen-specific manner by preferentially targeting effector T cells while preserving regulatory T cells. However, translation to the clinic proved to be more difficult than expected. New generation CD3 antibodies, currently used in phase II/III trials in autoimmunity, constitute a promising approach as, beside their immunosuppressive effect, they also express potent tolerogenic capacities. Importantly, CD3 therapy is effective especially when applied in primed hosts, highlighting the importance of the therapeutic window for tolerance induction.
SUMMARY: Further investigations are required for adapting to the clinic monoclonal antibodies as substitutes for current immunosuppression. Our aim is to show that development of new therapeutic strategies/molecules may come from transversal-type research, in particular from experience in autoimmunity, as immune responses leading to autoimmunity and graft rejection involve similar pathways.

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Year:  2010        PMID: 20881491     DOI: 10.1097/MOT.0b013e3283402bd8

Source DB:  PubMed          Journal:  Curr Opin Organ Transplant        ISSN: 1087-2418            Impact factor:   2.640


  6 in total

1.  Anti-CD3ε mAb improves thymic architecture and prevents autoimmune manifestations in a mouse model of Omenn syndrome: therapeutic implications.

Authors:  Veronica Marrella; Pietro L Poliani; Elena Fontana; Anna Casati; Virginia Maina; Barbara Cassani; Francesca Ficara; Manuela Cominelli; Francesca Schena; Marianna Paulis; Elisabetta Traggiai; Paolo Vezzoni; Fabio Grassi; Anna Villa
Journal:  Blood       Date:  2012-06-21       Impact factor: 22.113

2.  Anti-TCRβ mAb induces long-term allograft survival by reducing antigen-reactive T cells and sparing regulatory T cells.

Authors:  Y Miyahara; M Khattar; P M Schroder; B Mierzejewska; R Deng; R Han; W W Hancock; W Chen; S M Stepkowski
Journal:  Am J Transplant       Date:  2012-03-15       Impact factor: 8.086

3.  Autologous dendritic cells prolong allograft survival through Tmem176b-dependent antigen cross-presentation.

Authors:  M Segovia; C Louvet; P Charnet; A Savina; G Tilly; L Gautreau; L Carretero-Iglesia; G Beriou; I Cebrian; T Cens; L Hepburn; E Chiffoleau; R A Floto; I Anegon; S Amigorena; M Hill; M C Cuturi
Journal:  Am J Transplant       Date:  2014-04-14       Impact factor: 8.086

4.  TCR Signaling Emerges from the Sum of Many Parts.

Authors:  Michael S Kuhns; Mark M Davis
Journal:  Front Immunol       Date:  2012-06-25       Impact factor: 7.561

5.  MicroRNA expression profiles in human CD3+ T cells following stimulation with anti-human CD3 antibodies.

Authors:  Isabel Garcia Sousa; Manuela Maragno do Almo; Kelly Cristina Rodrigues Simi; Maryani Andressa Gomes Bezerra; Rosângela Vieira Andrade; Andréa Queiroz Maranhão; Marcelo Macedo Brigido
Journal:  BMC Res Notes       Date:  2017-03-14

6.  Delayed anti-CD3 therapy results in depletion of alloreactive T cells and the dominance of Foxp3+ CD4+ graft infiltrating cells.

Authors:  R Goto; S You; M Zaitsu; L Chatenoud; K J Wood
Journal:  Am J Transplant       Date:  2013-06-10       Impact factor: 8.086

  6 in total

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