Agency
National Institute of Health (NIH)
Institute
Fogarty International Center (FIC)
Type
International Research Fellowships (FIC) (F05)
Project #
1F05TW004418-01
Application #
3022011
Study Section
International and Cooperative Projects 1 Study Section (ICP)
Project Start
1990-09-30
Project End
Budget Start
1990-09-28
Budget End
1991-09-27
Support Year
1
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Brigham and Women's Hospital
Department
Type
DUNS #
071723621
City
Boston
State
MA
Country
United States
Zip Code
02115
Miller, A; Lider, O; Abramsky, O et al. (1994) Orally administered myelin basic protein in neonates primes for immune responses and enhances experimental autoimmune encephalomyelitis in adult animals. Eur J Immunol 24:1026-32
al-Sabbagh, A; Miller, A; Santos, L M et al. (1994) Antigen-driven tissue-specific suppression following oral tolerance: orally administered myelin basic protein suppresses proteolipid protein-induced experimental autoimmune encephalomyelitis in the SJL mouse. Eur J Immunol 24:2104-9
Miller, A; al-Sabbagh, A; Santos, L M et al. (1993) Epitopes of myelin basic protein that trigger TGF-beta release after oral tolerization are distinct from encephalitogenic epitopes and mediate epitope-driven bystander suppression. J Immunol 151:7307-15
Miller, A; Zhang, Z J; Sobel, R A et al. (1993) Suppression of experimental autoimmune encephalomyelitis by oral administration of myelin basic protein. VI. Suppression of adoptively transferred disease and differential effects of oral vs. intravenous tolerization. J Neuroimmunol 46:73-82
Miller, A; Lider, O; Roberts, A B et al. (1992) Suppressor T cells generated by oral tolerization to myelin basic protein suppress both in vitro and in vivo immune responses by the release of transforming growth factor beta after antigen-specific triggering. Proc Natl Acad Sci U S A 89:421-5
Miller, A; Lider, O; al-Sabbagh, A et al. (1992) Suppression of experimental autoimmune encephalomyelitis by oral administration of myelin basic protein. V. Hierarchy of suppression by myelin basic protein from different species. J Neuroimmunol 39:243-50