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Influence of splenectomy on first set rejection reactions of C57BL/6 females to male skin isografts

The tempo with which C57BL/6 females reject male skin isografts is determined in part by the immunogenicity of the H-Y antigen and in part by the capacity of the host to respond immunologically. Our studies indicate that the spleen plays an important role in determining the briskness of the rejectio...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1977
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2180801/
https://www.ncbi.nlm.nih.gov/pubmed/19553
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description The tempo with which C57BL/6 females reject male skin isografts is determined in part by the immunogenicity of the H-Y antigen and in part by the capacity of the host to respond immunologically. Our studies indicate that the spleen plays an important role in determining the briskness of the rejection process in that splenectomy 7-30 days before grafting with male skin significantly shortens the survival time. The results of reconstitution experiments suggests that a population of cells is present in spleens of normal, but not specifically sensitized, females which can restore the conventional first set reaction in splenectomized females. It is inferred that this resident population normally operates in spleen-intact females to delay the development of specific effector responses. Lymphoid cells from H-Y antigen- sensitized, splenectomized females failed to evoke graft-vs.-host responses in males whereas similar cells from females with spleens intact did possess graft-vs.-host potential.
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spelling pubmed-21808012008-04-17 Influence of splenectomy on first set rejection reactions of C57BL/6 females to male skin isografts J Exp Med Articles The tempo with which C57BL/6 females reject male skin isografts is determined in part by the immunogenicity of the H-Y antigen and in part by the capacity of the host to respond immunologically. Our studies indicate that the spleen plays an important role in determining the briskness of the rejection process in that splenectomy 7-30 days before grafting with male skin significantly shortens the survival time. The results of reconstitution experiments suggests that a population of cells is present in spleens of normal, but not specifically sensitized, females which can restore the conventional first set reaction in splenectomized females. It is inferred that this resident population normally operates in spleen-intact females to delay the development of specific effector responses. Lymphoid cells from H-Y antigen- sensitized, splenectomized females failed to evoke graft-vs.-host responses in males whereas similar cells from females with spleens intact did possess graft-vs.-host potential. The Rockefeller University Press 1977-09-01 /pmc/articles/PMC2180801/ /pubmed/19553 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
Influence of splenectomy on first set rejection reactions of C57BL/6 females to male skin isografts
title Influence of splenectomy on first set rejection reactions of C57BL/6 females to male skin isografts
title_full Influence of splenectomy on first set rejection reactions of C57BL/6 females to male skin isografts
title_fullStr Influence of splenectomy on first set rejection reactions of C57BL/6 females to male skin isografts
title_full_unstemmed Influence of splenectomy on first set rejection reactions of C57BL/6 females to male skin isografts
title_short Influence of splenectomy on first set rejection reactions of C57BL/6 females to male skin isografts
title_sort influence of splenectomy on first set rejection reactions of c57bl/6 females to male skin isografts
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2180801/
https://www.ncbi.nlm.nih.gov/pubmed/19553