Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program Projects (P01)
Project #
7P01AI037935-02
Application #
2074832
Study Section
Special Emphasis Panel (SRC (76))
Project Start
1995-06-01
Project End
1998-05-31
Budget Start
1996-06-01
Budget End
1997-05-31
Support Year
2
Fiscal Year
1996
Total Cost
Indirect Cost
Name
Trudeau Institute, Inc.
Department
Type
DUNS #
City
Saranac Lake
State
NY
Country
United States
Zip Code
12983
Rogers, P R; Dubey, C; Swain, S L (2000) Qualitative changes accompany memory T cell generation: faster, more effective responses at lower doses of antigen. J Immunol 164:2338-46
Swain, S L (2000) CD4 T-cell memory can persist in the absence of class II. Philos Trans R Soc Lond B Biol Sci 355:407-11
Bradley, L M; Harbertson, J; Watson, S R (1999) Memory CD4 cells do not migrate into peripheral lymphnodes in the absence of antigen. Eur J Immunol 29:3273-84
Bradley, L M; Asensio, V C; Schioetz, L K et al. (1999) Islet-specific Th1, but not Th2, cells secrete multiple chemokines and promote rapid induction of autoimmune diabetes. J Immunol 162:2511-20
Carter, L L; Swain, S L (1998) From naive to memory. Development and regulation of CD4+ T cell responses. Immunol Res 18:1-13
Carter, L L; Zhang, X; Dubey, C et al. (1998) Regulation of T cell subsets from naive to memory. J Immunother 21:181-7
Rogers, P R; Huston, G; Swain, S L (1998) High antigen density and IL-2 are required for generation of CD4 effectors secreting Th1 rather than Th0 cytokines. J Immunol 161:3844-52
Dutton, R W; Bradley, L M; Swain, S L (1998) T cell memory. Annu Rev Immunol 16:201-23
Bradley, L M; Malo, M E; Fong, S et al. (1998) Blockade of both L-selectin and alpha4 integrins abrogates naive CD4 cell trafficking and responses in gut-associated lymphoid organs. Int Immunol 10:961-8
Klinman, N R (1997) The cellular origins of memory B cells. Semin Immunol 9:241-7

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