Research Project
Grant-in-Aid for Young Scientists (B)
CD22-/-mice showed delayed recovery from CHS reactions compared with wild type mice. Our current study reveals a defect in survival or retention in activated CD22-/-peritoneal B-1 cells and a regulatory role of peritoneal B-1a cells in CHS. Comparing with CHS in CD19-/-mice revealed that peritoneal B-1a cells are likely to suppress the late remission phase as "regulatory B cells". CD22 deficiency results in disturbed CHS remission by impaired retention or survival of peritoneal B-1a cells that migrate into lymphoid organs.
All 2011 2010
All Journal Article (3 results) (of which Peer Reviewed: 2 results)
The Journal of Immunology
Volume: 184巻 Pages: 4637-4645
皮膚病診療
Volume: 33巻7号 Pages: 680-685
Volume: 184 Pages: 4637-4645