The overall objectives of this Lymphocyte Biology Program Project grant are to provide Core Facilities to support the research programs of member investigators which through individual research grants pursue a better understanding of fundamental mechanisms of the immune response in terms of: life histories of immunocompetent cells and macrophages; the genetic and phenotypic factors which determine their function; the biochemistry, genetics and functions of products of major histocompatibility and immunoglobulin heavy and light chain gene complexes; the nature of receptors on immunocompetent cells; and, the diverss mechanisms regulating immune responses. These objectives will be pursued through multi-disciplinary and collaborative research programs involving 17 investigators in 12 laboratory units. The major themes of these research programs are: the biology of macrophages, T cells and B cells; the genetics, chemistry and function of their recognition units, associated membrane components and secreted products (receptors for antigen, MHC gene complex products, helper and suppressor T cell products and antibodies); and, the mechanisms by which all these components interact to regulate development and expression of immune responses. These research programs constitute an integrated approach to gain a better understanding of immune response mechanisms at their cellular and molecular levels as they function in normal nd pathological situations. This research effort will be supported by five key core facilities: 1) Animal Production Facility; 1) Hybridoma Facility; 3) Protein Chemistry Facility; 4) Special Cell Facility; and 5) Shared Personnel Facility. These Core Facilities will be used extensively by member investigators and constitute unique and essential research support resources that cannot be supported by any single or smaller collection of investigators.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program Projects (P01)
Project #
5P01AI015353-10
Application #
3091462
Study Section
(SRC)
Project Start
1987-05-01
Project End
1992-04-30
Budget Start
1988-05-01
Budget End
1989-04-30
Support Year
10
Fiscal Year
1988
Total Cost
Indirect Cost
Name
Barnes-Jewish Hospital
Department
Type
DUNS #
City
Saint Louis
State
MO
Country
United States
Zip Code
63110
Lisbona, Fernanda; Rojas-Rivera, Diego; Thielen, Peter et al. (2009) BAX inhibitor-1 is a negative regulator of the ER stress sensor IRE1alpha. Mol Cell 33:679-91
Zimecki, M; Kapp, J A (1995) Presentation of antigen by B cell subsets. V. Effect of interleukin 7 (IL-7) and interleukin 10 (IL-10) on phenotype and antigen presenting function of immature B cells. Arch Immunol Ther Exp (Warsz) 43:253-7
Zimecki, M; Kapp, J A (1994) Presentation of antigen by B cell subsets. IV. Defective T-B cell signalling causes inability to present antigen by B cells from immunodeficient mice. Arch Immunol Ther Exp (Warsz) 42:361-7
Zimecki, M; Kapp, J A (1994) Presentation of antigen by B cell subsets. II. The role of CD5 B cells in the presentation of antigen to antigen-specific T cells. Arch Immunol Ther Exp (Warsz) 42:349-53
Zimecki, M; Kapp, J A (1994) Presentation of antigen by B cell subsets. III. Effects of interleukins on antigen presenting function and phenotype of immature B cells. Arch Immunol Ther Exp (Warsz) 42:355-9
Zimecki, M; Whiteley, P J; Pierce, C W et al. (1994) Presentation of antigen by B cells subsets. I. Lyb-5+ and Lyb-5- B cells differ in ability to stimulate antigen specific T cells. Arch Immunol Ther Exp (Warsz) 42:115-23
Fuller, K A; Kanagawa, O; Nahm, M H (1993) T cells within germinal centers are specific for the immunizing antigen. J Immunol 151:4505-12
Poindexter, N J; Landon, C; Whiteley, P J et al. (1992) Comparison of the T cell receptors on insulin-specific hybridomas from insulin transgenic and nontransgenic mice. Loss of a subpopulation of self-reactive clones. J Immunol 149:38-44
Kennedy, J D; Pierce, C W; Lake, J P (1992) Extrathymic T cell maturation. Phenotypic analysis of T cell subsets in nude mice as a function of age. J Immunol 148:1620-9
Madassery, J V; Gillard, B; Marcus, D M et al. (1991) Subpopulations of B cells in germinal centers. III. HJ6, a monoclonal antibody, binds globoside and a subpopulation of germinal center B cells. J Immunol 147:823-9

Showing the most recent 10 out of 128 publications