Kaaijk P, Troost D, Dast P K, van den Berg F, Leenstra S, Bosch D A
Department of Neurosurgery, Academic Medical Centre, Amsterdam, The Netherlands.
Neuropathol Appl Neurobiol. 1995 Oct;21(5):392-8. doi: 10.1111/j.1365-2990.1995.tb01076.x.
Knowledge about lymphokine-activated killer (LAK) cell infiltration and LAK cell cytotoxicity is essential to improve the effectiveness of LAK cell therapy against gliomas. In the present study, organotypic multicellular spheroids (OMS) of glioma tissue were used as a culture model to study the effects of LAK cells on gliomas. Compared to tumour cell lines and spheroids derived from tumour cell lines, OMS have several advantages with respect to preservation of tumour cell heterogeneity and the maintenance of the tumour architecture, e.g. capillaries and extracellular matrix. Four glioma specimens, obtained at surgery, were cultured directly on agarose to form OMS, which were then co-cultured with either autologous LAK cells or autologous non-activated peripheral blood lymphocytes (PBLs). After various time periods of co-cultivation, the OMS were fixed and examined both histologically and immunocytochemically. The present results showed that LAK cells infiltrated the OMS completely within 24 h of co-cultivation and severe cellular damage was observed, whereas PBLs infiltrated the OMS poorly and there was only marginal cellular damage. The present study indicates that OMS of gliomas provide an experimental model to investigate the infiltration and cytotoxicity of LAK cells on glioma tissue in vitro.
了解淋巴因子激活的杀伤(LAK)细胞浸润和LAK细胞细胞毒性对于提高LAK细胞治疗胶质瘤的有效性至关重要。在本研究中,胶质瘤组织的器官型多细胞球体(OMS)被用作培养模型,以研究LAK细胞对胶质瘤的影响。与肿瘤细胞系和源自肿瘤细胞系的球体相比,OMS在保留肿瘤细胞异质性和维持肿瘤结构(如毛细血管和细胞外基质)方面具有几个优点。手术获取的四个胶质瘤标本直接在琼脂糖上培养以形成OMS,然后将其与自体LAK细胞或自体未激活的外周血淋巴细胞(PBL)共培养。共培养不同时间段后,固定OMS并进行组织学和免疫细胞化学检查。目前的结果表明,LAK细胞在共培养24小时内完全浸润OMS,并观察到严重的细胞损伤,而PBL对OMS的浸润较差,仅存在轻微的细胞损伤。本研究表明,胶质瘤的OMS提供了一个实验模型,用于体外研究LAK细胞对胶质瘤组织的浸润和细胞毒性。