2007
Lymphocyte showing the phenotype of regulatory T-cells infiltrate colon carcinoma
GARAJOVÁ, Ingrid, Pavel FABIAN, Rudolf NENUTIL, Ondřej SLABÝ, Ilona KOCÁKOVÁ et. al.Základní údaje
Originální název
Lymphocyte showing the phenotype of regulatory T-cells infiltrate colon carcinoma
Název česky
Lymfocyty vykazujíci fenotyp T-regulačných buněk infiltrují karcinom střeva
Autoři
GARAJOVÁ, Ingrid (703 Slovensko), Pavel FABIAN (203 Česká republika), Rudolf NENUTIL (203 Česká republika), Ondřej SLABÝ (203 Česká republika), Ilona KOCÁKOVÁ (203 Česká republika), Peter GRELL (703 Slovensko), Zina HANZELKOVÁ (203 Česká republika), Marek SVOBODA (203 Česká republika) a Rostislav VYZULA (203 Česká republika, garant)
Vydání
Abstract book. 2007
Další údaje
Jazyk
angličtina
Typ výsledku
Konferenční abstrakt
Obor
30200 3.2 Clinical medicine
Stát vydavatele
Itálie
Utajení
není předmětem státního či obchodního tajemství
Kód RIV
RIV/00216224:14110/07:00019123
Organizační jednotka
Lékařská fakulta
Klíčová slova anglicky
regulatory T-cells; colon carcinoma
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 9. 4. 2010 14:57, prof. RNDr. Ondřej Slabý, Ph.D.
V originále
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.
Česky
Publikace je pouze v anglickém jazyku.
Návaznosti
NR9076, projekt VaV |
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