Induction of obliterative airway disease by anti-HLA class I antibodies
- PMID: 16095491
- DOI: 10.1111/j.1600-6143.2005.00999.x
Induction of obliterative airway disease by anti-HLA class I antibodies
Abstract
Anti-HLA class I Abs are associated with the development of bronchiolitis obliterans syndrome (BOS) after lung transplantation. BOS is characterized histologically by fibrosis and airway epithelial cell apoptosis. We have previously shown that anti-HLA class I Abs induce proliferation, growth factor production and apoptosis in airway epithelial cells in vitro. Thus, this study was designed to determine whether anti-HLA class I Abs alone could induce obliterative airway disease (OAD) in heterotopic murine tracheal allografts. Toward this, HLA-A*0201-transgenic tracheal allografts were transplanted into Rag1-deficient mice treated with the W6/32 anti-HLA class I mAb. Allografts were harvested at days +30, +45, +60 and +90. Allografts displayed epithelial metaplasia by day +45, epithelial destruction and mild cellular infiltration by day +60 and complete lumen obliteration and moderate cellular infiltration by day +90. Anti-HLA class I Abs induced the production of several growth factors and growth factor receptors and apoptosis of parenchymal cells in the allograft. In addition, anti-HLA class I Abs induced macrophages and granulocytes infiltration. The results from this study demonstrate that anti-HLA class I Abs play an important role in the pathogenesis of OAD by inducing growth factor production, apoptosis and chemotaxis of inflammatory cells.
Similar articles
-
Interplay between immune responses to HLA and non-HLA self-antigens in allograft rejection.Hum Immunol. 2013 Nov;74(11):1478-85. doi: 10.1016/j.humimm.2013.07.002. Epub 2013 Jul 19. Hum Immunol. 2013. PMID: 23876679 Free PMC article. Review.
-
Indirect recognition and antibody production against a single mismatched HLA-A2-transgenic molecule precede the development of obliterative airway disease in murine heterotopic tracheal allografts.Transplantation. 2002 Jan 27;73(2):186-93. doi: 10.1097/00007890-200201270-00006. Transplantation. 2002. PMID: 11821728
-
Different kinetics of obliterative airway disease development in heterotopic murine tracheal allografts induced by CD4+ and CD8+ T cells.Transplantation. 2002 Sep 15;74(5):646-51. doi: 10.1097/00007890-200209150-00010. Transplantation. 2002. PMID: 12352880
-
Anti-HLA class I antibody binding to airway epithelial cells induces production of fibrogenic growth factors and apoptotic cell death: a possible mechanism for bronchiolitis obliterans syndrome.Hum Immunol. 2003 May;64(5):521-9. doi: 10.1016/s0198-8859(03)00038-7. Hum Immunol. 2003. PMID: 12691702
-
Molecular mechanisms of chronic rejection following transplantation.Immunol Res. 2005;32(1-3):179-85. doi: 10.1385/IR:32:1-3:179. Immunol Res. 2005. PMID: 16106068 Review.
Cited by
-
Interplay between immune responses to HLA and non-HLA self-antigens in allograft rejection.Hum Immunol. 2013 Nov;74(11):1478-85. doi: 10.1016/j.humimm.2013.07.002. Epub 2013 Jul 19. Hum Immunol. 2013. PMID: 23876679 Free PMC article. Review.
-
C4d deposition and cellular infiltrates as markers of acute rejection in rat models of orthotopic lung transplantation.Transplantation. 2008 Jul 15;86(1):123-9. doi: 10.1097/TP.0b013e31817b0b57. Transplantation. 2008. PMID: 18622289 Free PMC article.
-
An important role for autoimmunity in the immunopathogenesis of chronic allograft rejection.Int J Immunogenet. 2012 Oct;39(5):373-80. doi: 10.1111/j.1744-313X.2012.01112.x. Epub 2012 Apr 10. Int J Immunogenet. 2012. PMID: 22486939 Free PMC article. Review.
-
HLA and lung transplantation.Front Med. 2019 Jun;13(3):298-313. doi: 10.1007/s11684-018-0636-x. Epub 2019 Jun 11. Front Med. 2019. PMID: 29974325 Review.
-
The link between major histocompatibility complex antibodies and cell proliferation.Transplant Rev (Orlando). 2011 Oct;25(4):154-66. doi: 10.1016/j.trre.2011.04.001. Epub 2011 Jul 30. Transplant Rev (Orlando). 2011. PMID: 21803559 Free PMC article. Review.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Research Materials