Contrary to expectations based on in vitro experiments, we previously found that pancreatic IL-10 did not inhibit autoimmune diabetes but accelerated it in an MHC-dependent manner. Therefore, the ability of IL-10 to overcome the absence of all non-MHC diabetes susceptibility (Idd) alleles was studied in transgenic mice expressing pancreatic IL-10 backcrossed to B10.H2g7 congenic mice, which have no Idd alleles other than NOD MHC (H2g7). IL-10 transgenic backcross 1 (BC1) mice with H2g7/g7 haplotype developed clear-cut insulitis and diabetes, but neither transgenic mice with the H2g/b haplotype nor nontransgenic BC1 mice did so. Further implicating IL-10 in autoimmune diabetes, anti-IL-10 antibody treatment inhibited the development of insulitis in NOD mice. These results suggest that IL-10 may be necessary and sufficient for producing autoimmune diabetes in conjunction with NOD MHC homozygosity and that some Idd genes may be related to the regulation of IL-10.
IL-10 is necessary and sufficient for autoimmune diabetes in conjunction with NOD MHC homozygosity.
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M S Lee, R Mueller, L S Wicker, L B Peterson, N Sarvetnick; IL-10 is necessary and sufficient for autoimmune diabetes in conjunction with NOD MHC homozygosity.. J Exp Med 1 June 1996; 183 (6): 2663–2668. doi: https://doi.org/10.1084/jem.183.6.2663
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