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Louis Horwitz

Researcher at Johns Hopkins University

Publications -  25
Citations -  681

Louis Horwitz is an academic researcher from Johns Hopkins University. The author has contributed to research in topics: Syngeneic Graft & CD8. The author has an hindex of 15, co-authored 25 publications receiving 677 citations.

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Development of graft-vs.-host disease-like syndrome in cyclosporine-treated rats after syngeneic bone marrow transplantation. I. Development of cytotoxic T lymphocytes with apparent polyclonal anti-Ia specificity, including autoreactivity.

TL;DR: Results suggested that the anti-class II autoreactive cell associated with syngeneic GVHD either recognizes a common class II determinant ("public" epitope) shared by multiple strains of rats, or was polyspecific with respect to "private" class IIeterminants.
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C6 produced by macrophages contributes to cardiac allograft rejection.

TL;DR: Results indicate that C6 produced by macrophages can cause significant tissue damage in hearts grafted to hosts after C6 reconstitution by bone marrow transplantation.
Journal Article

Characterization of the autoreactive T cell repertoire in cyclosporin- induced syngeneic graft-versus-host disease: A highly conserved repertoire mediates autoaggression

TL;DR: There was a pronounced shift in the expression of this determinant between CD4 and CD8 single positive thymocytes, suggesting that CsA may inhibit normal positive selection processes for MHC class I and class II reactive T cells.
Journal Article

Characterization of peripheral autoregulatory mechanisms that prevent development of cyclosporin-induced syngeneic graft-versus-host disease.

TL;DR: The studies reveal that although cyclosporin did not interfere with the effector function of the autoregulatory T cells, it prevented the reconstitution of the regulatory system after syngeneic bone marrow transplantation.
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Promiscuous recognition of major histocompatibility complex class II determinants in cyclosporine-induced syngeneic graft-versus-host disease: specificity of cytolytic effector T cells.

TL;DR: The results suggest that recognition of this highly conserved peptide along with the additional interaction between the flanking region and the T cell receptor may account for the promiscuous activity of the autologous/syngeneic GVHD autoreactive T cells.