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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...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1990
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188548/ https://www.ncbi.nlm.nih.gov/pubmed/2388039 |
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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 |