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1.
J Immunol ; 161(1): 375-84, 1998 Jul 01.
Article in English | MEDLINE | ID: mdl-9647246

ABSTRACT

TCR- and IgG-binding Fc receptors (Fc gamma R) mediate a variety of critical biologic activities including cytolysis via the structurally related zeta- and gamma-chains. In previous studies, we have described chimeric immune receptors (CIR) in which the ligand-binding domain of a heterologous receptor or Ab is fused directly to the cytoplasmic domain of the TCR zeta-chain. Such zeta-CIRs efficiently trigger cytotoxic function of both T and NK cells in a target-specific manner. In this report, we compared the ability of both zeta- and gamma-CIRs to activate the cytolytic function of two distinct classes of Fc gamma R-bearing effectors, NK cells and neutrophils. Mature neutrophils expressing zeta- and gamma-CIR were generated in vivo from murine hemopoietic stem cells following transplantation of syngeneic mice with retrovirally transduced bone marrow or in vitro from transduced human CD34+ progenitors following differentiation. Both zeta- and gamma-based CIRs were capable of activating target-specific cytolysis by both NK cells and neutrophils, although the zeta-CIR was consistently more efficient. The experimental approach described is a powerful one with which to study the role of nonlymphoid effector cells in the host immune system and permits the rational design of immunotherapeutic strategies that rely on harnessing multiple immune cell functions via CIR-modified hemopoietic stem cells or progenitors.


Subject(s)
Cytotoxicity, Immunologic/immunology , Killer Cells, Natural/immunology , Membrane Proteins/biosynthesis , Neutrophils/immunology , Receptors, Antigen, T-Cell, gamma-delta/biosynthesis , Receptors, Antigen, T-Cell/biosynthesis , Recombinant Fusion Proteins/biosynthesis , Recombinant Fusion Proteins/immunology , Signal Transduction/immunology , Adult , Animals , Bone Marrow Cells/immunology , Bone Marrow Cells/metabolism , Bone Marrow Transplantation/immunology , Cell Differentiation/genetics , Cell Differentiation/immunology , Cytotoxicity Tests, Immunologic , Epitopes, T-Lymphocyte/immunology , Female , Genetic Vectors/chemical synthesis , Humans , Killer Cells, Natural/metabolism , Male , Membrane Proteins/genetics , Membrane Proteins/immunology , Mice , Mice, SCID , Moloney murine leukemia virus/genetics , Moloney murine leukemia virus/immunology , Neutrophils/cytology , Neutrophils/metabolism , Protein Structure, Tertiary , Receptors, Antigen, T-Cell/genetics , Receptors, Antigen, T-Cell/immunology , Receptors, Antigen, T-Cell, gamma-delta/genetics , Receptors, Antigen, T-Cell, gamma-delta/immunology , Recombinant Fusion Proteins/genetics , Signal Transduction/genetics , Transduction, Genetic/immunology
6.
J Exp Med ; 184(6): 2261-9, 1996 Dec 01.
Article in English | MEDLINE | ID: mdl-8976181

ABSTRACT

Gene modification of hematopoietic stem cells (HSC) with antigen-specific, chimeric, or "universal" immune receptors (URs) is a novel but untested form of targeted immunotherapy. A human immunodeficiency virus (HIV) envelope-specific UR consisting of the extracellular domain of human CD4 linked to the zeta chain of the T cell receptor (CD4 zeta) was introduced ex vivo into murine HSC by retroviral transduction. After transplantation into immunodeficient SCID mice, sustained high level expression of CD4 zeta was observed in circulating myeloid and natural killer cells. CD4 zeta-transplanted mice were protected from challenge with a lethal dose of a disseminated human leukemia expressing HIV envelope. These results demonstrate the ability of chimeric receptors bearing zeta-signaling domains to activate non-T cell effector populations in vivo and thereby mediate systemic immunity.


Subject(s)
Bone Marrow Transplantation/immunology , CD4 Antigens/immunology , Gene Products, env/immunology , HIV/immunology , Membrane Proteins/immunology , Receptors, Antigen, T-Cell/immunology , T-Lymphocytes/immunology , Animals , Cell Line , Cytotoxicity, Immunologic , DNA Primers , Female , Gene Products, env/biosynthesis , Graft Survival/immunology , Humans , Male , Mice , Mice, SCID , Neutrophils/physiology , Polymerase Chain Reaction , Transplantation, Heterologous/immunology
7.
Skeletal Radiol ; 24(7): 523-7, 1995 Oct.
Article in English | MEDLINE | ID: mdl-8545650

ABSTRACT

The trapeziometacarpal joint is particularly prone to osteoarthritis due to the great amount of stress applied with everyday activities with the hands. In this essay, radiologic assessment and staging of "basal joint" osteoarthritis, treatments based on radiologic staging and intraoperative findings, and surgical complications are described.


Subject(s)
Osteoarthritis/diagnostic imaging , Thumb/diagnostic imaging , Wrist Joint/diagnostic imaging , Humans , Osteoarthritis/surgery , Osteoarthritis/therapy , Radiography
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