Dullens H F, Rademakers L H, Doffemont M, Van Veen P T, Bulder R, Den Otter W
Department of Pathology, University Hospital, Utrecht, The Netherlands.
Invasion Metastasis. 1993;13(5):267-76.
The omental lymphoid organ (OLO) is a part of the greater omentum composed of vascularized spots containing lymphocytes, plasma cells and macrophages located in a regular pattern between fat cells. To gain insight in the involvement of the OLO in the induction of immunity against tumor cells in the peritoneal cavity, we studied the penetration of tumor cells into the OLO after intraperitoneal, subcutaneous and intravenous injection. Furthermore we analyzed the tumoricidal activity of macrophages isolated from the OLO. Our results indicate that the OLO is only infiltrated by tumor cells directly from the peritoneal cavity, but not by subcutaneously or intravenously injected tumor cells unless they have reached the peritoneal cavity. Bromodeoxy-uridine labelled tumor cells can be detected in the OLO within 10 min after i.p. injection. The penetration is facilitated by the induction of fenestrations between the mesothelial cells (lining the OLO) after intraperitoneal injection of the tumor cells. These fenestrations can also be seen after nonspecific stimulation of the peritoneal cavity. Macrophages isolated from the OLO of mice immunized against syngeneic as well as allogeneic tumor cells express a significant cytotoxicity, which (at least in the syngeneic situation) precedes the cytotoxicity of the macrophages isolated from the peritoneal cavity. In conclusion, our data support the hypothesis that immune reactions against intraperitoneally injected tumor cells are initiated in the OLO leading to 'peritoneal immunity' against these tumor cells.
大网膜淋巴器官(OLO)是大网膜的一部分,由富含淋巴细胞、浆细胞和巨噬细胞的血管化斑点组成,这些细胞以规则的模式分布在脂肪细胞之间。为了深入了解OLO在诱导针对腹腔内肿瘤细胞的免疫反应中的作用,我们研究了肿瘤细胞经腹腔、皮下和静脉注射后向OLO的浸润情况。此外,我们分析了从OLO分离的巨噬细胞的杀瘤活性。我们的结果表明,OLO仅被直接来自腹腔的肿瘤细胞浸润,皮下或静脉注射的肿瘤细胞除非已到达腹腔,否则不会浸润OLO。腹腔注射后10分钟内即可在OLO中检测到溴脱氧尿苷标记的肿瘤细胞。腹腔注射肿瘤细胞后,间皮细胞(衬于OLO)之间形成窗孔,促进了肿瘤细胞的浸润。在对腹腔进行非特异性刺激后也可观察到这些窗孔。从免疫了同基因和异基因肿瘤细胞的小鼠的OLO中分离的巨噬细胞表现出显著的细胞毒性,(至少在同基因情况下)这种细胞毒性先于从腹腔分离的巨噬细胞的细胞毒性。总之,我们的数据支持这样的假设,即针对腹腔内注射肿瘤细胞的免疫反应在OLO中启动,从而导致对这些肿瘤细胞的“腹腔免疫”。