Cargando…

Transfer of human systemic lupus erythematosus in severe combined immunodeficient (SCID) mice

To study the role of peripheral blood leukocytes (PBL) in the pathogenesis of human systemic lupus erythematosus (SLE), we transferred PBL from 5 SLE patients into 15 severe combined immunodeficiency (SCID) mice. Such reconstituted mice showed long-term presence of auto-antibodies characteristic of...

Descripción completa

Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1990
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188548/
https://www.ncbi.nlm.nih.gov/pubmed/2388039
_version_ 1782146434290679808
collection PubMed
description To study the role of peripheral blood leukocytes (PBL) in the pathogenesis of human systemic lupus erythematosus (SLE), we transferred PBL from 5 SLE patients into 15 severe combined immunodeficiency (SCID) mice. Such reconstituted mice showed long-term presence of auto-antibodies characteristic of the donor in their sera, as well as human immunoglobulin deposition, and in some cases mouse C3, in the renal glomeruli. SCID mice repopulated with PBLs from normal donors do not develop serologic abnormalities or immunodeposits. It is concluded that human SLE serology and some associated renal changes can be reproduced solely by PBL transferred from afflicted patients, and that SCID-human-SLE mice may serve as an in vivo laboratory model for the study of human SLE.
format Text
id pubmed-2188548
institution National Center for Biotechnology Information
language English
publishDate 1990
publisher The Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-21885482008-04-17 Transfer of human systemic lupus erythematosus in severe combined immunodeficient (SCID) mice J Exp Med Articles To study the role of peripheral blood leukocytes (PBL) in the pathogenesis of human systemic lupus erythematosus (SLE), we transferred PBL from 5 SLE patients into 15 severe combined immunodeficiency (SCID) mice. Such reconstituted mice showed long-term presence of auto-antibodies characteristic of the donor in their sera, as well as human immunoglobulin deposition, and in some cases mouse C3, in the renal glomeruli. SCID mice repopulated with PBLs from normal donors do not develop serologic abnormalities or immunodeposits. It is concluded that human SLE serology and some associated renal changes can be reproduced solely by PBL transferred from afflicted patients, and that SCID-human-SLE mice may serve as an in vivo laboratory model for the study of human SLE. The Rockefeller University Press 1990-09-01 /pmc/articles/PMC2188548/ /pubmed/2388039 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Transfer of human systemic lupus erythematosus in severe combined immunodeficient (SCID) mice
title Transfer of human systemic lupus erythematosus in severe combined immunodeficient (SCID) mice
title_full Transfer of human systemic lupus erythematosus in severe combined immunodeficient (SCID) mice
title_fullStr Transfer of human systemic lupus erythematosus in severe combined immunodeficient (SCID) mice
title_full_unstemmed Transfer of human systemic lupus erythematosus in severe combined immunodeficient (SCID) mice
title_short Transfer of human systemic lupus erythematosus in severe combined immunodeficient (SCID) mice
title_sort transfer of human systemic lupus erythematosus in severe combined immunodeficient (scid) mice
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188548/
https://www.ncbi.nlm.nih.gov/pubmed/2388039