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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
1994
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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 |
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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 |
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