Rockett J C, Darnton S J, Crocker J, Matthews H R, Morris A G
Department of Biological Sciences, University of Warwick, Coventry.
J Clin Pathol. 1996 Mar;49(3):264-7. doi: 10.1136/jcp.49.3.264.
Infiltration by T lymphocytes into oesophageal carcinomas was assessed immunohistochemically, total T lymphocyte numbers by staining for CD3 and activated T lymphocytes by staining for CD25. Five squamous carcinomas and seven adenocarcinomas, resected without neoadjuvant treatment, were studied. Computer aided quantitation showed that total numbers of tumour infiltrating CD3 positive cells were highly variable (range 48-1673 cells/mm2). They were located largely in the stromal (87.9-99.2%) rather than intratumoral regions. Up to 84% of tumour infiltrating T lymphocytes were CD25 positive, although the median figure was 33%. There was no correlation between T lymphocyte infiltration or activation and expression of class I and II histocompatibility antigens, intercellular adhesion molecule-1, tumour stage or grade. These results imply that the local inflammatory response in oesophageal carcinomas is deregulated, which may be a factor contributing to the aggressive nature of the tumours.
通过免疫组织化学方法评估T淋巴细胞浸润食管癌的情况,用CD3染色评估总T淋巴细胞数量,用CD25染色评估活化T淋巴细胞数量。研究了5例未接受新辅助治疗而切除的鳞状细胞癌和7例腺癌。计算机辅助定量分析显示,肿瘤浸润的CD3阳性细胞总数变化很大(范围为48 - 1673个细胞/mm²)。它们主要位于间质(87.9 - 99.2%)而非肿瘤内区域。高达84%的肿瘤浸润T淋巴细胞为CD25阳性,尽管中位数为33%。T淋巴细胞浸润或活化与I类和II类组织相容性抗原、细胞间粘附分子-1的表达、肿瘤分期或分级之间无相关性。这些结果表明食管癌中的局部炎症反应失调,这可能是导致肿瘤侵袭性的一个因素。