This is a request for a second renewal of a program project that has involved most of the principles for over eight years. Because of the reorientation of the NIAlD program under which this program project has been funded for the last decade a clinically oriented Demonstration Project has been added and because the focus has increasingly become inflammation (as opposed to the pure genetics of the major histocompatibility complex in man) an additional project has been added. Critical cells of the immune system are being studied in four distinct projects (T cells, macrophages, mast cells and B cells). The role of the major histocompatibility complex, T cell receptors, and antigen presentation are central elements of the immune system and of inflammation. The effector cells of this system, the macrophages and mast cells are also being studied. All of us have shared reagents, technologies, ideas and resources for some years and the addition of a Demonstration Project that is related to a chronic inflammatory disease is a reasonable and natural outgrowth of this longstanding interaction. Core facilities which serve to facilitate interaction as well as promote the sharing of resources are essential. As such, the broad goals of our program should be realizable.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project--Cooperative Agreements (U01)
Project #
5U01AI034621-02
Application #
2069782
Study Section
Special Emphasis Panel (SRC (25))
Project Start
1993-08-01
Project End
1997-07-31
Budget Start
1994-08-01
Budget End
1995-07-31
Support Year
2
Fiscal Year
1994
Total Cost
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
City
Dallas
State
TX
Country
United States
Zip Code
75390
Zwirner, N W; Marcos, C Y; Mirbaha, F et al. (2000) Identification of MICA as a new polymorphic alloantigen recognized by antibodies in sera of organ transplant recipients. Hum Immunol 61:917-24
Lin, M S; Fu, C L; Aoki, V et al. (2000) Desmoglein-1-specific T lymphocytes from patients with endemic pemphigus foliaceus (fogo selvagem). J Clin Invest 105:207-13
Zwirner, N W; Dole, K; Stastny, P (1999) Differential surface expression of MICA by endothelial cells, fibroblasts, keratinocytes, and monocytes. Hum Immunol 60:323-30
Boackle, S A; Morris, M A; Holers, V M et al. (1998) Complement opsonization is required for presentation of immune complexes by resting peripheral blood B cells. J Immunol 161:6537-43
Forero, L; Zwirner, N W; Fink, C W et al. (1998) Juvenile arthritis, HLA-A2 and binding of DEK oncogene-peptides. Hum Immunol 59:443-50
Zwirner, N W; Fernandez-Vina, M A; Stastny, P (1998) MICA, a new polymorphic HLA-related antigen, is expressed mainly by keratinocytes, endothelial cells, and monocytes. Immunogenetics 47:139-48
Marcos, C Y; Fernandez-Vina, M A; Lazaro, A M et al. (1997) Novel HLA-B35 subtypes: putative gene conversion events with donor sequences from alleles common in native Americans (HLA-B*4002 or B*4801). Hum Immunol 53:148-55
Fernandez-Vina, M A; Lazaro, A M; Marcos, C Y et al. (1997) Dissimilar evolution of B-locus versus A-locus and class II loci of the HLA region in South American Indian tribes. Tissue Antigens 50:233-50
Wang, J; Fernandez-Vina, M A; Lazaro, A M et al. (1997) New alleles of the HLA-B15 family. Hum Immunol 55:184-9
Boackle, S A; Holers, V M; Karp, D R (1997) CD21 augments antigen presentation in immune individuals. Eur J Immunol 27:122-9