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Immunohistochemical Evidence of the Involvement of Natural Killer (CD161+) Cells in Spontaneous Regression of Lewis Rat Sarcoma
J. Kovalska, M. Cervinkova, E. Chmelikova, D. Planska, J. Cizkova, V. Horak,
Language English Country Greece
Document type Journal Article
NLK
Free Medical Journals
from 2004 to 2 years ago
PubMed Central
from 2017
Europe PubMed Central
from 2017
Open Access Digital Library
from 2004-01-01
PubMed
30587601
DOI
10.21873/invivo.11437
Knihovny.cz E-resources
- MeSH
- Killer Cells, Natural pathology MeSH
- CD4-Positive T-Lymphocytes pathology MeSH
- CD8-Positive T-Lymphocytes pathology MeSH
- Immunohistochemistry MeSH
- Rats MeSH
- NK Cell Lectin-Like Receptor Subfamily B genetics MeSH
- Humans MeSH
- Disease Models, Animal MeSH
- Rats, Inbred Lew MeSH
- Gene Expression Regulation, Neoplastic MeSH
- Sarcoma genetics pathology MeSH
- Neoplasm Regression, Spontaneous genetics pathology MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
BACKGROUND/AIM: Spontaneous regression (SR) of tumours is a rare phenomenon not yet fully understood. The aim of this study was to investigate immune cells infiltrating progressive and SR tumours in a Lewis rat sarcoma model. MATERIALS AND METHODS: Rats were subcutaneously inoculated with rat sarcoma R5-28 (clone C4) cells. Developing tumours were obtained on day 42 and cryosections were immunohistochemically processed for detection of immune cells. RESULTS: A high density of granulocytes was found in the necrotic areas of both progressive and SR tumours. CD4+ cells and CD8+ cells were rare and sparsely dispersed in the tumour tissue without clear difference between the two types of tumours. On the contrary, CD161+ cells were abundant and evenly distributed in SR tumours, but these cells were very rare in progressive tumours. CONCLUSION: Based on the differences in number and distribution of the immune cell subpopulations, we believe that natural killer (CD161+) cells play a major role in the destruction of cancer cells during SR of tumours in this Lewis rat model.
References provided by Crossref.org
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