Identification of a new subset of cells exhibiting dendritic phenotypes in patients affected by breast proliferative disorders

• Published in: Human immunology 2000-08, Vol.61 (8), p.739-752
• Main Authors: D’Apice, Luciana, De Berardinis, Piergiuseppe, Pasquinelli, Rosa, Capasso, Immacolata, D’Aiuto, Massimiliano, D’Aiuto, Giuseppe, Anzisi, Anna Maria, Favre, Reneé, Cermola, Michele, Barba, Pasquale, Guardiola, John
• Format: Article
• Language: English
• Subjects: Adult; Antibodies, Monoclonal - immunology; blood; Breast Neoplasms - blood; Breast Neoplasms - immunology; Breast Neoplasms - ultrastructure; Carcinoma, Ductal, Breast - blood; Carcinoma, Ductal, Breast - immunology; Carcinoma, Ductal, Breast - ultrastructure; CD14 antigen; CD34 antigen; dendritic cells; Dendritic Cells - classification; Dendritic Cells - immunology; Dendritic Cells - ultrastructure; electron microscopy; Endocytosis - immunology; FACS; Female; Fetal Blood - cytology; Fetal Blood - immunology; Humans; Immunophenotyping; Leukocytes, Mononuclear - classification; Leukocytes, Mononuclear - immunology; Leukocytes, Mononuclear - ultrastructure; Microscopy, Electron; Middle Aged; Staining and Labeling - methods; tumor immunity
• ISSN: 0198-8859; 1879-1166
• DOI: 10.1016/S0198-8859(00)00141-5

We report that a subset of circulating cells reacting with a monoclonal antibody raised against a protein marker is significantly increased in the peripheral blood of women carrying benign or malignant breast diseases, particularly in patients under 55 years of age with ductal mammary carcinomas. These cells were statistically (confidence level of 99%) less represented in a control population including healthy women or women carrying carcinomas of origin other than breast. Double staining analysis showed that they harbor markers of dendritic cells and exhibit endo- cytic activity, as determined by their ability to internalize FITC-dextran particles. Their dendritic morphology was further demonstrated by electron microscopy of sorted antibody-positive cells. However, expression of surface molecules, such as CD34 and CD14, usually not present in differentiated populations of dendritic cells was also observed. Adherent cells of patients with breast ductal carcinoma including mostly cells of this new subset were efficient stimulators of mixed lymphocyte reaction, attaining maximal stimulatory activity attained after TNFα treatment. In conclusion, we have shown that a subset of cells characterized by a phenotype suggestive of a yet undescribed stage of maturation of the dendritic cell lineage is accumulated in the blood of patients affected by breast proliferative disorders.