Skip to content
2000
Volume 4, Issue 1
  • ISSN: 1566-5240
  • E-ISSN: 1875-5666

Abstract

The MHC class I molecule, HLA-B27 can be expressed as a number of non-conventional forms, in addition to conventional HLA-B27 heterodimers presenting peptide. This has lead to new avenues of research to explain the association of this molecule with SpA. Surprisingly, HLA-B27 transgenic animal models implicated CD4+ T cells, which conventionally interact with MHC class II molecules, not MHC class I molecules, in the pathogenesis of SpA. One hypothesis to explain these finding is that non-conventional forms of HLA-B27, specifically HLA-B27 homodimers, might mimic MHC class II molecules and be recognised by CD4+ T cells. We investigated whether CD4+ T cells from AS patients can interact with HLA-B27, discovering that indeed CD4+ T cells can interact with various forms of HLA-B27. Here we discuss how such interactions between HLA-B27 and CD4+ T cells could occur in vivo and potential contributions of such interactions to the pathogenesis of SpA.

Loading

Article metrics loading...

/content/journals/cmm/10.2174/1566524043479257
2004-02-01
2025-09-04
Loading full text...

Full text loading...

/content/journals/cmm/10.2174/1566524043479257
Loading

  • Article Type:
    Review Article
Keyword(s): HLA-B27; homodimers; hypothesis; T cells
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test