Increased expression of CD40 ligand on activated T cells of patients with colon cancer

被引:1
|
作者
Büning, C
Krüger, K
Sieber, T
Schoeler, D
Schriever, F
机构
[1] Humboldt Univ, Virchow Univ Hosp, Charite,Dept Haematol & Oncol, Med Klin Mit Schwerpunkt Hamatol & Onkol, D-13353 Berlin, Germany
[2] Humboldt Univ, Charite, Med Klin Mit Schwerpunkt Gastroenterol Hepatol &, D-10117 Berlin, Germany
[3] Klin Wartenberg, D-85456 Wartenberg, Germany
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D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Proper function of T lymphocytes is crucial for an effective destruction of cancer cells in vivo. Identifying the cell surface molecules on the T cells that may be involved in this antitumor response may help to elucidate immunological factors influencing the biology of human tumors. Experimental Design: Differences in the antigen expression profile of unstimulated and stimulated peripheral blood T-lymphocytes from patients with colon cancer and from normal controls were determined using flow cytometry. Results: Freshly isolated peripheral blood T cells of patients with colon cancer did not differ in their phenotype significantly from those of patients with nonmalignant diseases. In contrast, in vitro stimulated T cells of patients with colon cancer had a significantly increased expression of CD40 ligand (CD40L, CD154) compared with activated T cells of the control group; increased CD40L expression was also found in the CD4(+)- and CD8(+)-T-cell subpopulations. Conclusions: The data presented support additional studies investigating the role of CD40L in the immune response against colon carcinoma.
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页码:1147 / 1151
页数:5
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