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The role of subregions of the rat major histocompatibility complex in the rejection and passive enhancement of renal allografts
The laboratory recombinant haplotype H-1acl of the Norway rat has been used in studies of the rejection and passive enhancement of kidney allografts. While the full H-1a haplotype provoked acute rejection, neither of the isolated subregions, H-1Aa and H-1Ba, did so. It was also found that alloantise...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1979
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2184738/ https://www.ncbi.nlm.nih.gov/pubmed/368285 |
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collection | PubMed |
description | The laboratory recombinant haplotype H-1acl of the Norway rat has been used in studies of the rejection and passive enhancement of kidney allografts. While the full H-1a haplotype provoked acute rejection, neither of the isolated subregions, H-1Aa and H-1Ba, did so. It was also found that alloantisera raised against either the H-1Aa or the H- 1Ba antigens would enhance the grafts. It is suggested that both MHC subregions contain a histocompatibility locus (i) for kidney (as they do for skin) and that in the genetic combinations studied only incompatibility for both provokes a response sufficient for rejection. In other combinations, however, single region incompatibilities may be sufficient. |
format | Text |
id | pubmed-2184738 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1979 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21847382008-04-17 The role of subregions of the rat major histocompatibility complex in the rejection and passive enhancement of renal allografts J Exp Med Articles The laboratory recombinant haplotype H-1acl of the Norway rat has been used in studies of the rejection and passive enhancement of kidney allografts. While the full H-1a haplotype provoked acute rejection, neither of the isolated subregions, H-1Aa and H-1Ba, did so. It was also found that alloantisera raised against either the H-1Aa or the H- 1Ba antigens would enhance the grafts. It is suggested that both MHC subregions contain a histocompatibility locus (i) for kidney (as they do for skin) and that in the genetic combinations studied only incompatibility for both provokes a response sufficient for rejection. In other combinations, however, single region incompatibilities may be sufficient. The Rockefeller University Press 1979-01-01 /pmc/articles/PMC2184738/ /pubmed/368285 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 The role of subregions of the rat major histocompatibility complex in the rejection and passive enhancement of renal allografts |
title | The role of subregions of the rat major histocompatibility complex in the rejection and passive enhancement of renal allografts |
title_full | The role of subregions of the rat major histocompatibility complex in the rejection and passive enhancement of renal allografts |
title_fullStr | The role of subregions of the rat major histocompatibility complex in the rejection and passive enhancement of renal allografts |
title_full_unstemmed | The role of subregions of the rat major histocompatibility complex in the rejection and passive enhancement of renal allografts |
title_short | The role of subregions of the rat major histocompatibility complex in the rejection and passive enhancement of renal allografts |
title_sort | role of subregions of the rat major histocompatibility complex in the rejection and passive enhancement of renal allografts |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2184738/ https://www.ncbi.nlm.nih.gov/pubmed/368285 |