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Activation of the guinea pig alternative complement pathway by mouse IgA immune complexes
Activation of the complement system by IgA was investigated with immune complexes containing a mouse IgA myeloma protein with specificity for phosphorylcholine linked to bovine serum albumin (PC-BSA). These IgA anti-PC-BSA immune complexes activated the alternative complement pathway in mouse and gu...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1982
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2186569/ https://www.ncbi.nlm.nih.gov/pubmed/7054357 |
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collection | PubMed |
description | Activation of the complement system by IgA was investigated with immune complexes containing a mouse IgA myeloma protein with specificity for phosphorylcholine linked to bovine serum albumin (PC-BSA). These IgA anti-PC-BSA immune complexes activated the alternative complement pathway in mouse and guinea pig serum, while human complement was not affected. The activation proceeded with consumption of C3 but little or no consumption of C5. C3 did not bind to the IgA immune complexes during complement activation although it did bind covalently to IgG immune complexes. It is suggested that IgA immune complexes do not supply a suitable surface for C3 binding and effective alternative pathway convertase assembly; therefore, cleavage is limited and occurs primarily in the fluid phase. Without C3 binding, C5 cleavage does not occur nor can the alternative pathway activation proceed to the amplification step. |
format | Text |
id | pubmed-2186569 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1982 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21865692008-04-17 Activation of the guinea pig alternative complement pathway by mouse IgA immune complexes J Exp Med Articles Activation of the complement system by IgA was investigated with immune complexes containing a mouse IgA myeloma protein with specificity for phosphorylcholine linked to bovine serum albumin (PC-BSA). These IgA anti-PC-BSA immune complexes activated the alternative complement pathway in mouse and guinea pig serum, while human complement was not affected. The activation proceeded with consumption of C3 but little or no consumption of C5. C3 did not bind to the IgA immune complexes during complement activation although it did bind covalently to IgG immune complexes. It is suggested that IgA immune complexes do not supply a suitable surface for C3 binding and effective alternative pathway convertase assembly; therefore, cleavage is limited and occurs primarily in the fluid phase. Without C3 binding, C5 cleavage does not occur nor can the alternative pathway activation proceed to the amplification step. The Rockefeller University Press 1982-01-01 /pmc/articles/PMC2186569/ /pubmed/7054357 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 Activation of the guinea pig alternative complement pathway by mouse IgA immune complexes |
title | Activation of the guinea pig alternative complement pathway by mouse IgA immune complexes |
title_full | Activation of the guinea pig alternative complement pathway by mouse IgA immune complexes |
title_fullStr | Activation of the guinea pig alternative complement pathway by mouse IgA immune complexes |
title_full_unstemmed | Activation of the guinea pig alternative complement pathway by mouse IgA immune complexes |
title_short | Activation of the guinea pig alternative complement pathway by mouse IgA immune complexes |
title_sort | activation of the guinea pig alternative complement pathway by mouse iga immune complexes |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2186569/ https://www.ncbi.nlm.nih.gov/pubmed/7054357 |