Our objective is to breed transgenic animals that are to be used by the investigators in the projects of this Program Project Grant entitled: """"""""Murine Models of Human Immunodeficiencies"""""""". Several transgenic mice lines are already available for studies in core B. A number of these animals were generated at the Alt and Terhorst labs, others were obtained from colleagues for breeding purposes. Key mice that are already available include transgenic lines that lack T cells and NK cells (T-/NK- ), Rag-2 deficient mice which lack B immunodeficient mouse strains for the reasons stated in Project 1: Transgenic Models of T Cell Receptor Immunodeficiencies. COX TERHORST, Beth Israel Hospital. Project 2: HIGMX-1: Transgenic Models of CD40 and CD40L deficiency. Raif Geha and Fred rosen, Children's Hospital. Project 3: Murine XLA and SCID Models. Frederick ALT and Fred Rosen, The Center for blood Research. Specifically we propose to: 1. Set up rag-2 colony for far-2-/- blastocyst complementation studies in Projects 1, 2, and 3. 2. Breed transgenic mice generated in Projects 1, 2, and 3. 3. Generate novel mouse strains through interbreeding animals generated by the investigators in Projects 1, 2, and 3. 4. Conduct preliminary analyses of immunodeficient mice.

Project Start
Project End
Budget Start
Budget End
Support Year
2
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Beth Israel Deaconess Medical Center
Department
Type
DUNS #
076593722
City
Boston
State
MA
Country
United States
Zip Code
02215
Sayos, J; Wu, C; Morra, M et al. (2017) Pillars Article: The X-Linked Lymphoproliferative Disease Gene Product SAP Regulates Signals Induced through the Co-Receptor SLAM. Nature. 1998. 395: 462-469. J Immunol 199:1534-1541
Chaudhary, Anu; Leite, Mara; Kulasekara, Bridget R et al. (2016) Human Diversity in a Cell Surface Receptor that Inhibits Autophagy. Curr Biol 26:1791-801
Jabri, Bana; Terhorst, Cox (2014) Editorial overview: Autoimmunity. Curr Opin Immunol 31:v-vii
Sintes, Jordi; Cuenca, Marta; Romero, Xavier et al. (2013) Cutting edge: Ly9 (CD229), a SLAM family receptor, negatively regulates the development of thymic innate memory-like CD8+ T and invariant NKT cells. J Immunol 190:21-6
Detre, Cynthia; Keszei, Marton; Garrido-Mesa, Natividad et al. (2012) SAP expression in invariant NKT cells is required for cognate help to support B-cell responses. Blood 120:122-9
McDonald, Douglas R; Massaad, Michel J; Johnston, Alicia et al. (2010) Successful engraftment of donor marrow after allogeneic hematopoietic cell transplantation in autosomal-recessive hyper-IgE syndrome caused by dedicator of cytokinesis 8 deficiency. J Allergy Clin Immunol 126:1304-5.e3
McDonald, Douglas R; Goldman, Frederick; Gomez-Duarte, Oscar D et al. (2010) Impaired T-cell receptor activation in IL-1 receptor-associated kinase-4-deficient patients. J Allergy Clin Immunol 126:332-7, 337.e1-2
Detre, Cynthia; Keszei, Marton; Romero, Xavier et al. (2010) SLAM family receptors and the SLAM-associated protein (SAP) modulate T cell functions. Semin Immunopathol 32:157-71
Sintes, Jordi; Romero, Xavier; de Salort, Jose et al. (2010) Mouse CD84 is a pan-leukocyte cell-surface molecule that modulates LPS-induced cytokine secretion by macrophages. J Leukoc Biol 88:687-97
Diamond, Betty; Cunningham-Rundles, Charlotte; Fischer, Alain et al. (2010) Josiah F. Wedgwood (1950-2009). J Allergy Clin Immunol 125:506

Showing the most recent 10 out of 107 publications