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Changes in host immunity following excision of a murine melanoma.

Changes in cell mediated and humoral immunity following the excision of a transplantable melanoma growing in the footpad of its syngeneic host, as measured by an in vitro cytotoxicity test, were assessed. Spleen cell cytotoxicity did not change significantly. Cells from the regional lymph nodes stim...

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Detalles Bibliográficos
Autores principales: Bray, A. E., Keast, D.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1975
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2009396/
https://www.ncbi.nlm.nih.gov/pubmed/1164467
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author Bray, A. E.
Keast, D.
author_facet Bray, A. E.
Keast, D.
author_sort Bray, A. E.
collection PubMed
description Changes in cell mediated and humoral immunity following the excision of a transplantable melanoma growing in the footpad of its syngeneic host, as measured by an in vitro cytotoxicity test, were assessed. Spleen cell cytotoxicity did not change significantly. Cells from the regional lymph nodes stimulated tumour growth before tumour excision. Three days following tumour excision this stimulatory effect was undetectable. Loss of serum factors capable of blocking the cytotoxicity of spleen cells occurred 24 h after tumour excision. Serum cytotoxicity increased after tumour excision to a maximum of the third day. Following tumour excision the rise in serum cytotoxicity and loss of regional lymph node tumour stimulation were concomitant with the loss of blocking activity.
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spelling pubmed-20093962009-09-10 Changes in host immunity following excision of a murine melanoma. Bray, A. E. Keast, D. Br J Cancer Research Article Changes in cell mediated and humoral immunity following the excision of a transplantable melanoma growing in the footpad of its syngeneic host, as measured by an in vitro cytotoxicity test, were assessed. Spleen cell cytotoxicity did not change significantly. Cells from the regional lymph nodes stimulated tumour growth before tumour excision. Three days following tumour excision this stimulatory effect was undetectable. Loss of serum factors capable of blocking the cytotoxicity of spleen cells occurred 24 h after tumour excision. Serum cytotoxicity increased after tumour excision to a maximum of the third day. Following tumour excision the rise in serum cytotoxicity and loss of regional lymph node tumour stimulation were concomitant with the loss of blocking activity. Nature Publishing Group 1975-02 /pmc/articles/PMC2009396/ /pubmed/1164467 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Bray, A. E.
Keast, D.
Changes in host immunity following excision of a murine melanoma.
title Changes in host immunity following excision of a murine melanoma.
title_full Changes in host immunity following excision of a murine melanoma.
title_fullStr Changes in host immunity following excision of a murine melanoma.
title_full_unstemmed Changes in host immunity following excision of a murine melanoma.
title_short Changes in host immunity following excision of a murine melanoma.
title_sort changes in host immunity following excision of a murine melanoma.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2009396/
https://www.ncbi.nlm.nih.gov/pubmed/1164467
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