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Immunologgical self-tolerance in allophenic and embryo-aggregated mice

Allophenic mice, supposedly containing almost equal numbers of cells derived from embryos of mouse strains C57Bl and FVB, were shown in a recent paper to grow the B16 melanoma, a long transplanted tumor of C57Bl origin, much better than did mice of either the parental C57Bl strain or the C57Bl × FVB...

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Detalles Bibliográficos
Autores principales: Prehn, Richmond T, Prehn, Liisa M
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2949691/
https://www.ncbi.nlm.nih.gov/pubmed/20854686
http://dx.doi.org/10.1186/1742-4682-7-38
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author Prehn, Richmond T
Prehn, Liisa M
author_facet Prehn, Richmond T
Prehn, Liisa M
author_sort Prehn, Richmond T
collection PubMed
description Allophenic mice, supposedly containing almost equal numbers of cells derived from embryos of mouse strains C57Bl and FVB, were shown in a recent paper to grow the B16 melanoma, a long transplanted tumor of C57Bl origin, much better than did mice of either the parental C57Bl strain or the C57Bl × FVB F1 hybrid. Mice containing smaller proportions of C57Bl cells rejected the tumor. A reconsideration of these suprising data, in light of the current literature, suggests that the better growth of the tumor in the 50-50% allophenics than in the C57Bl parental strain was almost certainly caused by the tumor stimulation engendered by a weak anti-C57Bl immune reaction in the overtly healthy allophenic mice.
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spelling pubmed-29496912010-10-06 Immunologgical self-tolerance in allophenic and embryo-aggregated mice Prehn, Richmond T Prehn, Liisa M Theor Biol Med Model Commentary Allophenic mice, supposedly containing almost equal numbers of cells derived from embryos of mouse strains C57Bl and FVB, were shown in a recent paper to grow the B16 melanoma, a long transplanted tumor of C57Bl origin, much better than did mice of either the parental C57Bl strain or the C57Bl × FVB F1 hybrid. Mice containing smaller proportions of C57Bl cells rejected the tumor. A reconsideration of these suprising data, in light of the current literature, suggests that the better growth of the tumor in the 50-50% allophenics than in the C57Bl parental strain was almost certainly caused by the tumor stimulation engendered by a weak anti-C57Bl immune reaction in the overtly healthy allophenic mice. BioMed Central 2010-09-20 /pmc/articles/PMC2949691/ /pubmed/20854686 http://dx.doi.org/10.1186/1742-4682-7-38 Text en Copyright ©2010 Prehn and Prehn; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Commentary
Prehn, Richmond T
Prehn, Liisa M
Immunologgical self-tolerance in allophenic and embryo-aggregated mice
title Immunologgical self-tolerance in allophenic and embryo-aggregated mice
title_full Immunologgical self-tolerance in allophenic and embryo-aggregated mice
title_fullStr Immunologgical self-tolerance in allophenic and embryo-aggregated mice
title_full_unstemmed Immunologgical self-tolerance in allophenic and embryo-aggregated mice
title_short Immunologgical self-tolerance in allophenic and embryo-aggregated mice
title_sort immunologgical self-tolerance in allophenic and embryo-aggregated mice
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2949691/
https://www.ncbi.nlm.nih.gov/pubmed/20854686
http://dx.doi.org/10.1186/1742-4682-7-38
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