This is an application for partial funding of a conference on Lymphocytes and the Immune System: Molecular, Cellular and Integrative Mechanisms. This conference will be held under the auspices of FASEB at the Omni Resort, Tuscon, AZ on July 9-14, 2005. This conference is the second in a new series of FASEB Summer Research Conferences and is based upon a growing recognition that the immune system serves as a paradigm for understanding diverse biological processes including the regulation of cell fates, programmed gene rearrangements, genome stability, receptor mediated cell signaling and oncogenesis. Molecular, cellular and genetic characterization of the lymphocytes can provide new insights eukaryotic biology. Our proposed meeting is designed to highlight new investigative approaches and their applications to the analysis of the immune system and lymphocytes. This type of forum will illuminate cell biological and gene regulatory pathways that enable immune cell generation and function. To introduce the versatility of these new approaches we have included speakers who are world leaders in developing and applying cutting edge experimental approaches to a variety of systems as well as internationally recognized speakers who have directly applied these methods to the immune system. Approximately 150 participants will be chosen from among scientists most likely to share new information and to contribute to stimulating exchanges of ideas. The major session topics will be: 1) specification of immune cell fates, 2) antigen receptor gene rearrangements and DMA repair, 3) gene expression and locus accessibility in the immune system, 4) NF-kappaB and links between the innate and humoral immune systems, 5) gene regulatory networks and immune cell differentiation, 6) lymphocyte survival and transformation, 7) B and T cell activation, 8) regulation of immune responses, 9) microenvironments and lympho-organogenesis. There will be oral presentations of selected abstracts and two poster sessions. This conference will provide a forum for dialogue between scientists employing a broad variety of investigative approaches. The meeting will produce a contemporary perspective and overview of the immune system as well as a critical review of the recent research and will permit evaluation of future research directions.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Conference (R13)
Project #
5R13AI066870-04
Application #
7431682
Study Section
Special Emphasis Panel (ZAI1-MJH-M (M1))
Program Officer
Coulter, Nancy A
Project Start
2005-06-01
Project End
2010-05-31
Budget Start
2008-06-01
Budget End
2009-05-31
Support Year
4
Fiscal Year
2008
Total Cost
$1
Indirect Cost
Name
Federation of Amer Soc for Exper Biology
Department
Type
DUNS #
074816851
City
Bethesda
State
MD
Country
United States
Zip Code
20814
Langley, William A; Thoennes, Sudha; Bradley, Konrad C et al. (2009) Single residue deletions along the length of the influenza HA fusion peptide lead to inhibition of membrane fusion function. Virology 394:321-30
Cross, Karen J; Langley, William A; Russell, Rupert J et al. (2009) Composition and functions of the influenza fusion peptide. Protein Pept Lett 16:766-78
Meisner, Jeffrey; Szretter, Kristy J; Bradley, Konrad C et al. (2008) Infectivity studies of influenza virus hemagglutinin receptor binding site mutants in mice. J Virol 82:5079-83
Thoennes, Sudha; Li, Zhu-Nan; Lee, Byeong-Jae et al. (2008) Analysis of residues near the fusion peptide in the influenza hemagglutinin structure for roles in triggering membrane fusion. Virology 370:403-14
Li, Zhu-Nan; Lee, Byeong-Jae; Langley, William A et al. (2008) Length requirements for membrane fusion of influenza virus hemagglutinin peptide linkers to transmembrane or fusion peptide domains. J Virol 82:6337-48
Kemball, Christopher C; Pack, Christopher D; Guay, Heath M et al. (2007) The antiviral CD8+ T cell response is differentially dependent on CD4+ T cell help over the course of persistent infection. J Immunol 179:1113-21
Li, Min; Li, Zhu-Nan; Yao, Qizhi et al. (2006) Murine leukemia virus R Peptide inhibits influenza virus hemagglutinin-induced membrane fusion. J Virol 80:6106-14
Burleigh, Laura M; Calder, Lesley J; Skehel, John J et al. (2005) Influenza a viruses with mutations in the m1 helix six domain display a wide variety of morphological phenotypes. J Virol 79:1262-70
Li, Zhu-Nan; Mueller, Scott N; Ye, Ling et al. (2005) Chimeric influenza virus hemagglutinin proteins containing large domains of the Bacillus anthracis protective antigen: protein characterization, incorporation into infectious influenza viruses, and antigenicity. J Virol 79:10003-12