TY - JOUR
T1 - HLA-DRB5*0101 and -DRB1*1501 expression in the multiple sclerosis-associated HLA-DR15 haplotype
AU - Prat, Elisabetta
AU - Tomaru, Utano
AU - Sabater, Lidia
AU - Park, Deric M.
AU - Granger, Rebekah
AU - Kruse, Niels
AU - Ohayon, Joan M.
AU - Bettinotti, Maria P.
AU - Martin, Roland
N1 - Funding Information:
Elisabetta Prat was supported by a postdoctoral fellowship from the US National Multiple Sclerosis Society. We thank Dr. Ricardo Pujol-Borrell (Badalona, Spain) for kindly providing thymic tissues and advice on the analysis, Dr. Eduard Palou (Badalona, Spain) for tissue typing, Dr. William W. Kwok (Seattle, WA) and Dr. G. Nepom (Seattle, WA) for kindly providing HLA-DRB1*1501 and -DRB5*0101 plasmids and BLS cells, Dr. Cedric S. Raine for CNS tissues, Deborah Kauffman and James W. Naegle (DNA Sequencing Facility, NINDS, NIH). Anti-DR2a and -DR2b Ab were kindly provided by Dr. Jar-How Lee at One Lambda Inc. (Canoga Park, CA).
PY - 2005/10
Y1 - 2005/10
N2 - The HLA region, and particularly the DR15 haplotype (containing the two DRB* genes DRB1*1501 and DRB5*0101 and the tightly linked DQ alleles DQA*0102 and DQB1*0602, which together form the DQw6 molecule) in Caucasians, shows the strongest genetic association with multiple sclerosis (MS). In the DR15 haplotype, two β-chains HLA-DRB1*1501 and -DRB5*0101 are co-expressed resulting in two different surface HLA-DR αβ heterodimers, DR2b and DR2a. Most previous studies focused on DRB1*1501, however, both DR2a and DR2b may contribute to MS pathogenesis via antigen presentation to myelin-specific T lymphocytes. We therefore analyzed the expression of the two DR15 genes in various antigen presenting cells (APCs), central nervous system and thymic tissues. Transcript levels were higher for DRB5*0101 in all cell types and tissues. Both HLA-DR heterodimers were expressed at significant levels on the cell surface, where they showed a differential expression pattern in different APCs. They were similarly regulated after stimulation with interferon-γ and interleukin-4. Finally, immunohistochemistry experiments indicated that both molecules were expressed in thymic tissue. Our results encourage future research to investigate the potential functional relevance of both genes for the pathogenesis of MS.
AB - The HLA region, and particularly the DR15 haplotype (containing the two DRB* genes DRB1*1501 and DRB5*0101 and the tightly linked DQ alleles DQA*0102 and DQB1*0602, which together form the DQw6 molecule) in Caucasians, shows the strongest genetic association with multiple sclerosis (MS). In the DR15 haplotype, two β-chains HLA-DRB1*1501 and -DRB5*0101 are co-expressed resulting in two different surface HLA-DR αβ heterodimers, DR2b and DR2a. Most previous studies focused on DRB1*1501, however, both DR2a and DR2b may contribute to MS pathogenesis via antigen presentation to myelin-specific T lymphocytes. We therefore analyzed the expression of the two DR15 genes in various antigen presenting cells (APCs), central nervous system and thymic tissues. Transcript levels were higher for DRB5*0101 in all cell types and tissues. Both HLA-DR heterodimers were expressed at significant levels on the cell surface, where they showed a differential expression pattern in different APCs. They were similarly regulated after stimulation with interferon-γ and interleukin-4. Finally, immunohistochemistry experiments indicated that both molecules were expressed in thymic tissue. Our results encourage future research to investigate the potential functional relevance of both genes for the pathogenesis of MS.
KW - Antigen presenting cells
KW - Antigen presenting molecules
KW - MHC
KW - Multiple sclerosis
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U2 - 10.1016/j.jneuroim.2005.04.027
DO - 10.1016/j.jneuroim.2005.04.027
M3 - Article
C2 - 16111772
AN - SCOPUS:24144492777
SN - 0165-5728
VL - 167
SP - 108
EP - 119
JO - Journal of Neuroimmunology
JF - Journal of Neuroimmunology
IS - 1-2
ER -