We showed that both AIP-1 and AIP-2 reduced cardiac cellular infiltrate, and in future studies identification and quantification of CD4+ and CD8+ T cells, as well as CD4+CD25+Foxp3+ cells, will better characterize the inflammatory cell infiltrate and determine the correlation between tissue-specific T cell responses and peripheral T cell responses evaluated from splenocytes. The gene discussed is FOXP3; the disease is autoimmune pancreatitis.