Abstract
Introduction: Genetic associations of American sarcoidosis susceptibility implicate MHC class II allele, DRB1*1101. We previously reported immune recognition of Mycobacterium peptides from peripheral cells of 26 sarcoidosis subjects, 24 PPD- healthy volunteers, and eight with latent tuberculosis infection. Materials and Methods: In order to further link these genetic and immunologic pillars of sarcoidosis pathogenesis, we performed flow cytometry on these same subjects to identify the cells responsible for immune responses to ESAT-6 and katG peptides, followed by HLA typing to determine allelic associations with recognition. Discussion and Conclusion: Sarcoidosis CD4+ T cells were primarily responsible for the systemic responses. Recognition was inhibited by monoclonal antibody against HLA-DR and HLA-DQ, but not HLA-DP. Immune recognition of ESAT-6 peptide NNALQNLARTISEAG was associated with possession of DRB1*1101. ESAT-6 and katG presented by antigen-presenting cells expressing DRB1*1101-induced Th-1 responses from sarcoidosis T cells, thus providing a mechanistic insight for the association of HLA DRB1*1101 with sarcoidosis, and sarcoidosis T cell interaction with microbial antigens.
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Oswald-Richter, K., Sato, H., Hajizadeh, R., Shepherd, B. E., Sidney, J., Sette, A., … Drake, W. P. (2010). Mycobacterial ESAT-6 and katG are recognized by sarcoidosis CD4+ T Cells when presented by the American sarcoidosis susceptibility allele, DRB1*1101. Journal of Clinical Immunology, 30(1), 157–166. https://doi.org/10.1007/s10875-009-9311-y
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