GARAJOVÁ, Ingrid, Pavel FABIAN, Rudolf NENUTIL, Ondřej SLABÝ, Ilona KOCÁKOVÁ, Peter GRELL, Zina HANZELKOVÁ, Marek SVOBODA and Rostislav VYZULA. Lymphocyte showing the phenotype of regulatory T-cells infiltrate colon carcinoma. In Abstract book. 2007.
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Basic information
Original name Lymphocyte showing the phenotype of regulatory T-cells infiltrate colon carcinoma
Name in Czech Lymfocyty vykazujíci fenotyp T-regulačných buněk infiltrují karcinom střeva
Authors GARAJOVÁ, Ingrid (703 Slovakia), Pavel FABIAN (203 Czech Republic), Rudolf NENUTIL (203 Czech Republic), Ondřej SLABÝ (203 Czech Republic), Ilona KOCÁKOVÁ (203 Czech Republic), Peter GRELL (703 Slovakia), Zina HANZELKOVÁ (203 Czech Republic), Marek SVOBODA (203 Czech Republic) and Rostislav VYZULA (203 Czech Republic, guarantor).
Edition Abstract book. 2007.
Other information
Original language English
Type of outcome Conference abstract
Field of Study 30200 3.2 Clinical medicine
Country of publisher Italy
Confidentiality degree is not subject to a state or trade secret
RIV identification code RIV/00216224:14110/07:00019123
Organization unit Faculty of Medicine
Keywords in English regulatory T-cells; colon carcinoma
Tags colon carcinoma, regulatory T-cells
Tags International impact, Reviewed
Changed by Changed by: prof. RNDr. Ondřej Slabý, Ph.D., učo 42891. Changed: 9/4/2010 14:57.
Abstract
We have previously shown that colon carcinoma (CC) is infiltrated by FOXP3-positive lymphocytes. Although the transcription factor FOXP3 is claimed to be specific for regulatory T (TREG) cells, the canonical TREG population is known to show the CD4+ CD25+ (FOXP3+) immunophenotype. The aim of the current study was therefore to investigate whether FOXP3+ cells infiltrating CC coexpress indeed CD4 and CD25 molecules. Double-staining experiments were therefore performed on serial sections obtained from formalin-fixed, paraffin-embedded specimens of nine cases of CC. The CC infiltrate included numerous CD4+ as well as CD25+ cells; moreover CD4+ cells harboured both FOXP3+ and FOXP3- lymphocytes; similarly, CD25+ cells included both FOXP3+ and FOXP3- lymphocytes. Nevertheless, all the FOXP3+ cells showed simultaneously CD4-positivity; similarly, all the FOXP3+ cells showed simultaneously CD25-positivity. Thus, the FOXP3+ lymphocytes infiltrating CC are characterized by the coexpression of both CD4 and CD25 molecules, and show therefore an immunophenotype overlapping with that of standard CD4+CD25+FOXP3+ TREG cells. The presence of lymphocytes resembling TREG cells within the microenvironment of CC can explain why the CC tumour mass, despite being also infiltrated by cytolytic anti-tumour CD8+/CD4+ lymphocytes, shows however the well known capability to undergo fatal progression. Acknowledgment: This project is supported by Internal Grant Agency, Ministry of Health, Czech Republic. No.: NR/9076-4.
Abstract (in Czech)
Publikace je pouze v anglickém jazyku.
Links
NR9076, research and development projectName: Genomické profilování v predikci odpovědi na chemoradioterapii u pacientů s lokálně pokročilým karcinomem konečníku
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