PMID- 15197496 OWN - NLM STAT- MEDLINE DCOM- 20041124 LR - 20240426 IS - 0340-7004 (Print) IS - 1432-0851 (Electronic) IS - 0340-7004 (Linking) VI - 53 IP - 11 DP - 2004 Nov TI - Dendritic cells in colorectal cancer correlate with other tumor-infiltrating immune cells. PG - 978-86 AB - Dendritic cells (DCs) are the most efficient antigen-presenting cells and play a key role in a cellular antitumor immune response. In this study we investigated the exact localization of DCs within colorectal tumors and their relationship to tumor-infiltrating lymphocytes as well as clinical outcome of the patients. Primary tumor specimens of 104 patients with a diagnosis of colorectal cancer were identified retrospectively and analyzed with the dendritic cell markers S-100 protein and human leukocyte antigens (HLA) class II. The markers were individually combined with laminin as a second marker to facilitate the observation of the different tumor localizations. S-100 or HLA class II positive cells were found in the three different compartments of colorectal tumors: tumor epithelium, tumor stroma, and advancing tumor margin, but mainly present in tumor stroma and advancing tumor margin. S-100-positive tumor-infiltrating DCs in direct contact with tumor cells, i.e., in tumor epithelium, significantly correlated to the intraepithelial infiltration of CD4+ (p=0.02) and CD8+ (p=0.01) lymphocytes. High HLA class II+ cell infiltration in the tumor stroma correlated to a lower intraepithelial infiltration of CD8+ (p=0.02) lymphocytes. High intraepithelial infiltration of S-100-positive DCs suggested increased disease-free survival, but was not statistically significant, while high amounts of HLA class II+ cells in the tumor stroma correlated with an adverse survival outcome. Our results show that the infiltration of DCs in colorectal cancer, depending on both location and type of marker, is correlated with local immune interactions and patient prognosis, suggesting a central role for DCs in controlling local tumor immunity. FAU - Dadabayev, A R AU - Dadabayev AR AD - Department of Surgery, Leiden University Medical Center, PO Box 9600, 2300 RC, Leiden, The Netherlands. FAU - Sandel, M H AU - Sandel MH FAU - Menon, A G AU - Menon AG FAU - Morreau, H AU - Morreau H FAU - Melief, C J M AU - Melief CJ FAU - Offringa, R AU - Offringa R FAU - van der Burg, S H AU - van der Burg SH FAU - Janssen-van Rhijn, C AU - Janssen-van Rhijn C FAU - Ensink, N G AU - Ensink NG FAU - Tollenaar, R A E M AU - Tollenaar RA FAU - van de Velde, C J H AU - van de Velde CJ FAU - Kuppen, P J K AU - Kuppen PJ LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20040617 PL - Germany TA - Cancer Immunol Immunother JT - Cancer immunology, immunotherapy : CII JID - 8605732 RN - 0 (Histocompatibility Antigens Class II) RN - 0 (Laminin) RN - 0 (S100 Proteins) SB - IM MH - Adult MH - Aged MH - Antigen-Presenting Cells/metabolism MH - CD4-Positive T-Lymphocytes/immunology/metabolism MH - CD8-Positive T-Lymphocytes/metabolism MH - Cell Line, Tumor MH - Colorectal Neoplasms/*immunology/*metabolism MH - Dendritic Cells/*cytology/immunology/metabolism MH - Disease-Free Survival MH - Epithelium/metabolism MH - Female MH - Follow-Up Studies MH - Histocompatibility Antigens Class II/*chemistry MH - Humans MH - Immunohistochemistry MH - Laminin/chemistry MH - Lymphocytes/metabolism MH - Male MH - Middle Aged MH - Retrospective Studies MH - S100 Proteins/*biosynthesis/chemistry MH - Time Factors MH - Treatment Outcome PMC - PMC11042674 EDAT- 2004/06/16 05:00 MHDA- 2004/12/16 09:00 PMCR- 2004/06/17 CRDT- 2004/06/16 05:00 PHST- 2003/12/15 00:00 [received] PHST- 2004/04/06 00:00 [accepted] PHST- 2004/06/16 05:00 [pubmed] PHST- 2004/12/16 09:00 [medline] PHST- 2004/06/16 05:00 [entrez] PHST- 2004/06/17 00:00 [pmc-release] AID - 548 [pii] AID - 10.1007/s00262-004-0548-2 [doi] PST - ppublish SO - Cancer Immunol Immunother. 2004 Nov;53(11):978-86. doi: 10.1007/s00262-004-0548-2. Epub 2004 Jun 17.