Literature DB >> 14980810

Anti-CD40 ligand monoclonal antibody induces a permissive state, but not tolerance, for murine peripheral nerve allografts.

Michael J Brenner1, Thomas H H Tung, Susan E Mackinnon, Terence M Myckatyn, Daniel A Hunter, Thalachallour Mohanakumar.   

Abstract

Anti-CD40 ligand monoclonal antibody prevents the interaction between CD40 and its T-cell-based ligand, thereby resulting in selective inhibition of T cell costimulation without pan-T-cell suppression. This antibody has found application in several animal models of solid organ transplantation. This study investigated use of anti-CD40 ligand antibody to promote acceptance of nerve allografts. In Experiment 1, 40 BALB/cj mice with tibial nerve transplants were administered anti-CD40 ligand antibody, a control antibody, or no treatment. In Experiment 2, 40 BALB/cj mice underwent the same regimen as in Experiment 1, but were later challenged with a second nerve allograft 3 weeks after discontinuation of treatment. Animals treated with anti-CD40 ligand antibody in Experiment 1 exhibited improved functional recovery and greater mean fiber count, fiber density, and percent nerve fiber than animals treated with control antibody or no antibody (P < 0.05). These permissive effects on nerve regeneration were associated with immune unresponsiveness on Elispot assay. The benefit of anti-CD40 ligand therapy did not persist after withdrawal of treatment (Experiment 2). Active blockade of the CD40 costimulatory pathway with murine anti-CD40 ligand antibody therefore induces a permissive state conducive to nerve regeneration across allografts but does not establish long-term tolerance.

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Year:  2004        PMID: 14980810     DOI: 10.1016/j.expneurol.2003.10.002

Source DB:  PubMed          Journal:  Exp Neurol        ISSN: 0014-4886            Impact factor:   5.330


  7 in total

1.  Dynamic quantification of host Schwann cell migration into peripheral nerve allografts.

Authors:  Elizabeth L Whitlock; Terence M Myckatyn; Alice Y Tong; Andrew Yee; Ying Yan; Christina K Magill; Philip J Johnson; Susan E Mackinnon
Journal:  Exp Neurol       Date:  2010-07-12       Impact factor: 5.330

2.  Experience with nerve allograft transplantation.

Authors:  Ida K Fox; Susan E Mackinnon
Journal:  Semin Plast Surg       Date:  2007-11       Impact factor: 2.314

3.  The role of T helper cell differentiation in promoting nerve allograft survival with costimulation blockade.

Authors:  Wilson Z Ray; Rahul Kasukurthi; Esther M Papp; Amy M Moore; Andrew Yee; Daniel A Hunter; Nancy L Solowski; Thalachallour Mohanakumar; Susan E Mackinnon; Thomas H Tung
Journal:  J Neurosurg       Date:  2010-02       Impact factor: 5.115

4.  Role of timing in assessment of nerve regeneration.

Authors:  Michael J Brenner; Arash Moradzadeh; Terence M Myckatyn; Thomas H H Tung; Allen B Mendez; Daniel A Hunter; Susan E Mackinnon
Journal:  Microsurgery       Date:  2008       Impact factor: 2.425

5.  Multiple costimulatory blockade in the peripheral nerve allograft.

Authors:  Chau Y Tai; Renata V Weber; Susan E Mackinnon; Thomas H Tung
Journal:  Neurol Res       Date:  2009-06-30       Impact factor: 2.448

6.  Treatment modality affects allograft-derived Schwann cell phenotype and myelinating capacity.

Authors:  Ayato Hayashi; Arash Moradzadeh; Alice Tong; Cindy Wei; Sami H Tuffaha; Daniel A Hunter; Thomas H Tung; Alexander Parsadanian; Susan E Mackinnon; Terence M Myckatyn
Journal:  Exp Neurol       Date:  2008-04-25       Impact factor: 5.330

7.  A double-transgenic mouse used to track migrating Schwann cells and regenerating axons following engraftment of injured nerves.

Authors:  Ayato Hayashi; Jason W Koob; Daniel Z Liu; Alice Y Tong; Daniel A Hunter; Alexander Parsadanian; Susan E Mackinnon; Terence M Myckatyn
Journal:  Exp Neurol       Date:  2007-06-19       Impact factor: 5.330

  7 in total

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