The 220 KD isoform of CD45 recognized by the monoclonal antibody B220 is differentially expressed on lymphocyte subsets. Among B cells it appears to distinguish a subset of memory B cells as well as being expressed on non-isotype switched B cells that do not have a memory phenotype. Within the ALPS population, B220 is expressed on the characteristic alpha beta TcR double negative T cell. In addition, B220 positivity appears to herald lymphocyte apoptosis following lymphocyte activation. Finally, B220 expression is also noted on T cell large granular lymphocyte (LGL) leukemia. The expression of B220 represents a glycosylation modification of the CD45 molecule. These findings in the context of the specific clinical observations associated with B220 expression suggest that the control of CD45 glycosylation has a significant role in lymphcoyte homeostasis and trafficking. Current studies are being undertaken to further elucidate these issues.

Agency
National Institute of Health (NIH)
Institute
Clinical Center (CLC)
Type
Intramural Research (Z01)
Project #
1Z01CL010309-03
Application #
6675228
Study Section
(DLM)
Project Start
Project End
Budget Start
Budget End
Support Year
3
Fiscal Year
2002
Total Cost
Indirect Cost
Name
Clinical Center
Department
Type
DUNS #
City
State
Country
United States
Zip Code