Andersen L P, Blom J, Nielsen H
Department of Microbiology, Rigshospitalet, University of Copenhagen, Denmark.
APMIS. 1993 Jan;101(1):61-72.
Few studies have been carried out on the phagocytosis and killing of Helicobacter pylori by both polymorphonuclear leukocytes (PMNs) and monocytes. In this study, H. pylori was incubated for up to 60 min either alone or with phagocytes in the presence or absence of human serum. Both non-immune serum and immune serum were used. Reduction in the number of H. pylori, which corresponds to the killing of H. pylori, was analysed by a colony count and ultrastructural changes were studied by electron microscopy. No reduction in the number of H. pylori was found when the bacteria were incubated alone or with phagocytes in the absence of serum. It is remarkable that unopsonized H. pylori was phagocytosed. When immune serum was added to the suspensions of bacteria and phagocytes, the killing rate of H. pylori was found to depend on the ratio of H. pylori to phagocytes. Thus an excess of monocytes reduced the number of H. pylori, whereas an excess of PMNs resulted in complete killing of H. pylori. On incubation with PMNs and serum, ultrastructural changes were observed in the majority of the bacteria whether they were phagocytosed or not. Controls without serum did not show any changes in the morphology of H. pylori, indicating that components in the serum play an important role in the phagocytosis and killing of H. pylori. In contrast, several of the phagocytosed bacteria were found to be unaffected after incubation with monocytes and serum. Such preparations often contained large aggregates of platelets surrounding unaffected H. pylori. In the gastric mucosa, H. pylori is often found in excess as compared to the phagocytes. If these results can be compared to the situation in vivo, the phagocytes seem to be ineffective in the killing of H. pylori, and other immune mechanisms may therefore be of importance for the elimination of H. pylori from the gastric epithelium. The possible intracellular survival of H. pylori should be taken into account when treatment regimes for H. pylori infections are chosen.
关于多形核白细胞(PMN)和单核细胞对幽门螺杆菌的吞噬作用及杀伤作用的研究较少。在本研究中,幽门螺杆菌在有或无人类血清存在的情况下,单独或与吞噬细胞一起孵育长达60分钟。使用了非免疫血清和免疫血清。通过菌落计数分析与幽门螺杆菌杀灭相对应的幽门螺杆菌数量减少情况,并通过电子显微镜研究超微结构变化。当细菌单独孵育或在无血清情况下与吞噬细胞一起孵育时,未发现幽门螺杆菌数量减少。值得注意的是,未调理的幽门螺杆菌被吞噬。当将免疫血清添加到细菌和吞噬细胞的悬液中时,发现幽门螺杆菌的杀伤率取决于幽门螺杆菌与吞噬细胞的比例。因此,单核细胞过多会减少幽门螺杆菌数量,而PMN过多则会导致幽门螺杆菌被完全杀灭。与PMN和血清一起孵育时,无论细菌是否被吞噬,大多数细菌都观察到超微结构变化。无血清的对照未显示幽门螺杆菌形态有任何变化,表明血清中的成分在幽门螺杆菌的吞噬和杀伤中起重要作用。相比之下,发现一些被吞噬的细菌在与单核细胞和血清孵育后未受影响。此类制剂中常常含有围绕未受影响的幽门螺杆菌的大量血小板聚集体。在胃黏膜中,与吞噬细胞相比,幽门螺杆菌常常过量存在。如果这些结果能与体内情况相比较,吞噬细胞在杀灭幽门螺杆菌方面似乎无效,因此其他免疫机制对于从胃上皮中清除幽门螺杆菌可能很重要。在选择幽门螺杆菌感染的治疗方案时,应考虑幽门螺杆菌可能在细胞内存活的情况。