TY - JOUR A1 - Banat, Gamal-André A1 - Tretyn, Aleksandra A1 - Pullamsetti, Soni Savai A1 - Wilhelm, Jochen A1 - Weigert, Andreas A1 - Olesch, Catherine A1 - Ebel, Katharina A1 - Stiewe, Thorsten A1 - Grimminger, Friedrich A1 - Seeger, Werner A1 - Fink, Ludger A1 - Savai, Rajkumar T1 - Immune and inflammatory cell composition of human lung cancer stroma T2 - PLoS One N2 - Recent studies indicate that the abnormal microenvironment of tumors may play a critical role in carcinogenesis, including lung cancer. We comprehensively assessed the number of stromal cells, especially immune/inflammatory cells, in lung cancer and evaluated their infiltration in cancers of different stages, types and metastatic characteristics potential. Immunohistochemical analysis of lung cancer tissue arrays containing normal and lung cancer sections was performed. This analysis was combined with cyto-/histomorphological assessment and quantification of cells to classify/subclassify tumors accurately and to perform a high throughput analysis of stromal cell composition in different types of lung cancer. In human lung cancer sections we observed a significant elevation/infiltration of total-T lymphocytes (CD3+), cytotoxic-T cells (CD8+), T-helper cells (CD4+), B cells (CD20+), macrophages (CD68+), mast cells (CD117+), mononuclear cells (CD11c+), plasma cells, activated-T cells (MUM1+), B cells, myeloid cells (PD1+) and neutrophilic granulocytes (myeloperoxidase+) compared with healthy donor specimens. We observed all of these immune cell markers in different types of lung cancers including squamous cell carcinoma, adenocarcinoma, adenosquamous cell carcinoma, small cell carcinoma, papillary adenocarcinoma, metastatic adenocarcinoma, and bronchioloalveolar carcinoma. The numbers of all tumor-associated immune cells (except MUM1+ cells) in stage III cancer specimens was significantly greater than those in stage I samples. We observed substantial stage-dependent immune cell infiltration in human lung tumors suggesting that the tumor microenvironment plays a critical role during lung carcinogenesis. Strategies for therapeutic interference with lung cancer microenvironment should consider the complexity of its immune cell composition. Y1 - 2015 UR - http://publikationen.ub.uni-frankfurt.de/frontdoor/index/index/docId/39041 UR - https://nbn-resolving.org/urn:nbn:de:hebis:30:3-390411 SN - 1932-6203 N1 - Copyright: © 2015 Banat et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited VL - 10 IS - (9): e0139073 SP - 1 EP - 21 PB - PLoS CY - Lawrence, Kan. ER -