Rakhmilevich A L, Rakhimova M S
Biull Eksp Biol Med. 1989 Dec;108(12):721-4.
The intratumoral administration of lipopolysaccharide (LPS) and muramyl dipeptide (MDP) in combination, but not separately, resulted in necrosis and rejection of subcutaneous P815 mastocytoma nodules in DBA/2 mice with 30 to 40% survival. Previous sensibilization of animals by LPS + MDP, treatment by indomethacin, cyclophosphamide or syngeneic lymphocytes did not augment the immunotherapeutic action of LPS + MDP combination. Reinoculation of P815 cells into cured DBA/2 mice 8 months after the disappearance of the primary tumor led to rejection of new nodules with 50% survival rate. In LPS + MDP immunotherapy of these tumors two stages may be distinguished by a thrombo-necrotic stage and that of development of immunity.
联合而非单独瘤内注射脂多糖(LPS)和胞壁酰二肽(MDP),可导致DBA/2小鼠皮下P815肥大细胞瘤结节出现坏死并被排斥,存活率为30%至40%。此前用LPS + MDP使动物致敏、用吲哚美辛、环磷酰胺或同基因淋巴细胞进行治疗,均未增强LPS + MDP联合疗法的免疫治疗作用。在原发性肿瘤消失8个月后,将P815细胞重新接种到治愈的DBA/2小鼠体内,可导致新结节被排斥,存活率为50%。在这些肿瘤的LPS + MDP免疫治疗中,可分为血栓坏死阶段和免疫形成阶段两个阶段。