Localisation pattern of Foxp3+ regulatory T cells is associated with clinical behaviour in gastric cancer.
Localisation pattern of Foxp3+ regulatory T cells is associated with clinical behaviour in gastric cancer.
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DOI:
10.1038/sj.bjc.6604149
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发表时间:
2008-01-15
影响因子:
8.8
通讯作者:
Fujii, H.
中科院分区:
文献类型:
--
作者:
Mizukami, Y.;Kono, K.;Kawaguchi, Y.;Akaike, H.;Kamimura, K.;Sugai, H.;Fujii, H.
It has been reported that the population of regulatory T cells (T regs) is increased in tumour-infiltrating lymphocytes in cancer-bearing hosts. Recently, forkhead/winged helix transcription factor p3, Foxp3, is thought to be the most reliable marker of T regs. In the present study, we investigated the prevalence and localisation pattern of Foxp3+ cells in gastric cancer (n=80) by immunohistochemistry, in relation to the clinical outcome of gastric cancer patients. Immunohistochemical staining was performed with anti-Foxp3 mAb, and Foxp3+ cells were semiquantified. We divided all cases into two groups: Foxp3+-high (n=40) and Foxp3+-low (n=40) groups, by the median size of the population of Foxp3+ cells. Furthermore, in terms of the localisation pattern of accumulating Foxp3+ cells in tumours, we classified all cases into three groups: a peri-tumour group (n=30), a diffuse group (n=40), and a follicular group (n=10). As a result, although the populations of Foxp3+ cells in stage IV were significantly larger than those in stage I (P<0.05), there was no significant difference in survival between the patients with high and low population levels of Foxp3+ cells. However, survival in patients with a diffuse pattern of Foxp3+ cells was significantly poorer than in those with a peri-tumoral pattern. In conclusion, the localisation pattern, but not the population size, of Foxp3+ cells was significantly related to patient survival.
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DOI:
10.1084/jem.193.11.1303
发表时间:
2001-06-04
期刊:
The Journal of experimental medicine
影响因子:
--
作者:
Dieckmann D;Plottner H;Berchtold S;Berger T;Schuler G
通讯作者:
Schuler G
影响因子:
4.4
作者:
Misra, N;Bayry, J;Kaveri, SV
通讯作者:
Kaveri, SV
影响因子:
32.4
作者:
Fontenot, JD;Rasmussen, JP;Rudensky, AY
通讯作者:
Rudensky, AY
影响因子:
4.4
作者:
Smyth, MJ;Teng, MWL;Hayakawa, Y
通讯作者:
Hayakawa, Y
影响因子:
11.5
作者:
Badoual, C;Hans, S;Tartour, E
通讯作者:
Tartour, E