In breast carcinoma tissue, immature dendritic cells reside within the tumor, whereas mature dendritic cells are located in peritumoral areas

被引:435
作者
Bell, D
Chomarat, P
Broyles, D
Netto, G
Harb, GM
Lebecque, S
Valladeau, J
Davoust, J
Palucka, KA
Banchereau, J
机构
[1] Baylor Inst Immunol Res, Dallas, TX 75204 USA
[2] Baylor Univ, Med Ctr, Dept Pathol, Dallas, TX 75204 USA
[3] Schering Plough Lab Immunol Res, F-69571 Dardilly, France
关键词
breast cancer; dendritic cells; tumor immunity; MHC class II; chemokines;
D O I
10.1084/jem.190.10.1417
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We have analyzed the presence of immature and mature dendritic cells (DCs) within adenocarcinoma of the breast using immunohistochemistry. Immature DCS were defined by expression of CD1a-, Langerin-, and intracellular major histocompatibility complex class II-rich vesicles. Mature DCs were defined by expression of CD83 and DC-Lamp. Breast carcinoma cells were defined by morphology and/or cytokeratin expression. We demonstrate two levels of heterogeneity of DCs infiltrating breast carcinoma tissue: (a) immature CD1a(+) DCs, mostly of the Langerhans cell type (Langerin(+)), were retained within the tumor bed in 32/32 samples and (b) mature DCs, CD83(+) DC-Lamp(+), present in 20/32 samples, are confined to peritumoral areas. The high numbers of immature DCs found in the tumor may be best explained by high levels of macrophage inflammatory protein 3 alpha expression by virtually all tumor cells. Confirming the immature/mature DC compartmentalization pattern, in vitro-generated immature DCs adhere to the tumor cells, whereas mature DCs adhere selectively to peritumoral areas. In some cases, T cells are clustering around the mature DCs in peritumoral areas, thus resembling the DC-T cell clusters of secondary lymphoid organs, which are characteristic of ongoing immune reactions.
引用
收藏
页码:1417 / 1425
页数:9
相关论文
共 41 条
[1]   Tumor-specific killer cells in paraneoplastic cerebellar degeneration [J].
Albert, ML ;
Darnell, JC ;
Bender, A ;
Francisco, LM ;
Bhardwaj, N ;
Darnell, RB .
NATURE MEDICINE, 1998, 4 (11) :1321-1324
[2]   Dendritic cells and the control of immunity [J].
Banchereau, J ;
Steinman, RM .
NATURE, 1998, 392 (6673) :245-252
[3]   Dendritic cells [J].
Bell, D ;
Young, JW ;
Banchereau, J .
ADVANCES IN IMMUNOLOGY, VOL. 72, 1999, 72 :255-324
[4]  
Caux C, 1997, ADV EXP MED BIOL, V417, P21
[5]   CD34(+) hematopoietic progenitors from human cord blood differentiate along two independent dendritic cell pathways in response to GM-CSF+TNF alpha [J].
Caux, C ;
Vanbervliet, B ;
Massacrier, C ;
DezutterDambuyant, C ;
deSaintVis, B ;
Jacquet, C ;
Yoneda, K ;
Imamura, S ;
Schmitt, D ;
Banchereau, J .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (02) :695-706
[6]   Origin, maturation and antigen presenting function of dendritic cells [J].
Cella, M ;
Sallusto, F ;
Lanzavecchia, A .
CURRENT OPINION IN IMMUNOLOGY, 1997, 9 (01) :10-16
[7]  
Coventry BJ, 1997, ADV EXP MED BIOL, V417, P571
[8]   Onconeural antigens and the paraneoplastic neurologic disorders: At the intersection of cancer, immunity, and the brain [J].
Darnell, RB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (10) :4529-4536
[9]   A novel lysosome-associated membrane glycoprotein, DC-LAMP, induced upon DC maturation, is transiently expressed in MHC class II compartment [J].
de Saint-Vis, B ;
Vincent, J ;
Vandenabeele, S ;
Vanbervliet, B ;
Pin, JJ ;
Aït-Yahia, S ;
Patel, S ;
Mattei, MG ;
Banchereau, J ;
Zurawski, S ;
Davoust, J ;
Caux, C ;
Lebecque, S .
IMMUNITY, 1998, 9 (03) :325-336
[10]   Selective recruitment of immature and mature dendritic cells by distinct chemokines expressed in different anatomic sites [J].
Dieu, MC ;
Vanbervliet, B ;
Vicari, A ;
Bridon, JM ;
Oldham, E ;
Aït-Yahia, S ;
Brière, F ;
Zlotnik, A ;
Lebecque, S ;
Caux, C .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (02) :373-386