Cargando…

Therapeutic uses of recombinant complement protein inhibitors

In conclusion, it is apparent that researchers are poised at the threshold of developing inhibitors of complement activation from the molecules in the RCA family. By creating soluble forms of these protective proteins for in vivo administration, or by making transgenic animals expressing these prote...

Descripción completa

Detalles Bibliográficos
Autores principales: Kalli, Kimberly R., Hsu, Peihong, Fearon, Douglas T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 1994
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7101590/
https://www.ncbi.nlm.nih.gov/pubmed/8153875
http://dx.doi.org/10.1007/BF01837368
_version_ 1783511657184493568
author Kalli, Kimberly R.
Hsu, Peihong
Fearon, Douglas T.
author_facet Kalli, Kimberly R.
Hsu, Peihong
Fearon, Douglas T.
author_sort Kalli, Kimberly R.
collection PubMed
description In conclusion, it is apparent that researchers are poised at the threshold of developing inhibitors of complement activation from the molecules in the RCA family. By creating soluble forms of these protective proteins for in vivo administration, or by making transgenic animals expressing these proteins or their derivatives, it may be possible to inhibit complement-mediated pathology stemming from autoimmune disease, reperfusion injuries, and physical trauma. This technology combined with current attempts to protect allografts from cellular rejection with monoclonal antibodies against members of the integrin family of adhesion molecules [52] makes it possible that the excessive mortality due to the severe shortage of human donor organs could be overcome by the use of xenografts.
format Online
Article
Text
id pubmed-7101590
institution National Center for Biotechnology Information
language English
publishDate 1994
publisher Springer-Verlag
record_format MEDLINE/PubMed
spelling pubmed-71015902020-03-31 Therapeutic uses of recombinant complement protein inhibitors Kalli, Kimberly R. Hsu, Peihong Fearon, Douglas T. Springer Semin Immunopathol Article In conclusion, it is apparent that researchers are poised at the threshold of developing inhibitors of complement activation from the molecules in the RCA family. By creating soluble forms of these protective proteins for in vivo administration, or by making transgenic animals expressing these proteins or their derivatives, it may be possible to inhibit complement-mediated pathology stemming from autoimmune disease, reperfusion injuries, and physical trauma. This technology combined with current attempts to protect allografts from cellular rejection with monoclonal antibodies against members of the integrin family of adhesion molecules [52] makes it possible that the excessive mortality due to the severe shortage of human donor organs could be overcome by the use of xenografts. Springer-Verlag 1994 /pmc/articles/PMC7101590/ /pubmed/8153875 http://dx.doi.org/10.1007/BF01837368 Text en © Springer-Verlag 1994 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Kalli, Kimberly R.
Hsu, Peihong
Fearon, Douglas T.
Therapeutic uses of recombinant complement protein inhibitors
title Therapeutic uses of recombinant complement protein inhibitors
title_full Therapeutic uses of recombinant complement protein inhibitors
title_fullStr Therapeutic uses of recombinant complement protein inhibitors
title_full_unstemmed Therapeutic uses of recombinant complement protein inhibitors
title_short Therapeutic uses of recombinant complement protein inhibitors
title_sort therapeutic uses of recombinant complement protein inhibitors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7101590/
https://www.ncbi.nlm.nih.gov/pubmed/8153875
http://dx.doi.org/10.1007/BF01837368
work_keys_str_mv AT kallikimberlyr therapeuticusesofrecombinantcomplementproteininhibitors
AT hsupeihong therapeuticusesofrecombinantcomplementproteininhibitors
AT fearondouglast therapeuticusesofrecombinantcomplementproteininhibitors