The adhesion pathway defined by Alpha4Beta7 integrin and the mucosal vascular addressin (MAdCAM) has been demonstrated to be intimately involved in the homing of gut-specific lymphocytes from the vasculature to the gastrointestinal tract and associated lymphoid tissue and as such is believed to be involved in mucosal-specific lymphocyte recruitment. In this report, using a previously-characterized nonhuman primate model of ulcerative colitis, we demonstrate that a blocking monoclonal antibody Alpha4Beta7 integrin, when administered to chronically colitic animals, ameliorates inflammatory activity and rapidly improves stool consistency. Furthermore, using morphometric analysis of biopsy specimens, antibody therapy reduces the mucosal density of Alpha4Beta7+ lymphocytes and Alpha4Beta7- neutrophils and macrophages. These results suggest that the Alpha4Beta7 integrin represents a novel, potentially organ-specific, therapeutic target for the treatment of inflammatory bowel disease.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Primate Research Center Grants (P51)
Project #
5P51RR000168-35
Application #
3719065
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
35
Fiscal Year
1996
Total Cost
Indirect Cost
Name
Harvard University
Department
Type
DUNS #
082359691
City
Boston
State
MA
Country
United States
Zip Code
02115
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