Hürter T
Pneumologie. 1989 Mar;43(3):147-58.
The elimination (by human alveolar macrophages and pulmonary granulocytes) of one laboratory strain and one wild-type strain each of Staphylococcus aureus and Pseudomonas aeruginosa has been investigated in vitro. Administering 10(6) alveolar macrophages to 5 x 10(6) staphylococci leads to a reduction of viable colony-forming units (CFU) to 5.8 x 10(5) (L] (laboratory strain (L) and 6.9 x 10(5) (wild-type strain (W)) after 60 minutes. The corresponding values of Ps. aeruginosa are 4.3 x 10(6) (L) and 4.4 x 10(6) (W). The peak chemiluminescence values are 9, 160 (L) and 12,300 (W) counts/10(5) cells for Staph. aureus and 7,670 (L) and 8,950 (W) for Ps. aeruginosa. The addition of heat-inactivated serum increases the number of staphylococci observed within alveolar macrophages from 1.57 to 3.18 (L) and from 1.32 to 2.79 (W). Fresh serum enhances ingestion to 8.15 (L) and 9.73 (W) staphylococci/macrophage. The number of phagocytized pseudomonads in pure culture medium is 0.51 (L) and 0.46 (W) bacteria/macrophage. An increase by the addition of serum is not possible. While staphylococci adhere to the membrane of the macrophage over a wide area, the pseudomonads adhere to it in a highly circumscribed manner. The following ingestion steps do not differ from one organism to the other. After 60 minutes, cultivation of 10(6) granulocytes with 5 x 10(6) staphylococci leads to a reduction of the viable CFU to 7.5 x 10(5) (L) and 9.4 x 10(5) (W). In the case of Ps. aeruginosa, the number of surviving CFU is 4.5 x 10(6) (L) and 3.8 x 10(6) (W). After the addition of Staph. aureus, peak values of 37,800 (L) and 35,500 (W) counts/10(5) cells are measured. The corresponding values for Ps. aeruginosa are 28,900 (L) and 33,100 counts/10(5) cells (W). The addition of heat-inactivated serum leads, in the case of Staphylococcus aureus, to an increase in the ingestion of the laboratory strain from 1.07 to 1.94 and of the wild-type strain from 0.94 to 2.41 bacteria/granulocyte. Fresh serum brings about a further increase to 5.52 (L) and 4.82 (W). In the case of Ps. aeruginosa. 0.75 (L) and 0.69 (W) ingested bacteria/granulocyte are observed; the addition of serum fails to bring about any increase. In contrast to the staphylococci, pseudomonads adhere to the granulocyte membrane in a punctate manner only. No differences of ingestion are seen.
已经在体外研究了人肺泡巨噬细胞和肺粒细胞对金黄色葡萄球菌和铜绿假单胞菌的一个实验室菌株和一个野生型菌株的清除作用。将10⁶个肺泡巨噬细胞与5×10⁶个葡萄球菌混合,60分钟后,活菌落形成单位(CFU)减少到5.8×10⁵(实验室菌株(L))和6.9×10⁵(野生型菌株(W))。铜绿假单胞菌的相应值分别为4.3×10⁶(L)和4.4×10⁶(W)。金黄色葡萄球菌的化学发光峰值分别为9160(L)和12300(W)计数/10⁵个细胞,铜绿假单胞菌的化学发光峰值分别为7670(L)和8950(W)。添加热灭活血清后,肺泡巨噬细胞内观察到的葡萄球菌数量从1.57(L)增加到3.18(L),从1.32(W)增加到2.79(W)。新鲜血清使吞噬量增加到8.15(L)和9.73(W)个葡萄球菌/巨噬细胞。在纯培养基中,吞噬的假单胞菌数量为0.51(L)和0.46(W)个细菌/巨噬细胞。添加血清后无法增加吞噬量。葡萄球菌在巨噬细胞膜的大片区域附着,而假单胞菌以高度局限的方式附着。随后的吞噬步骤在不同生物体之间没有差异。60分钟后,将10⁶个粒细胞与5×10⁶个葡萄球菌培养,活菌CFU减少到7.5×10⁵(L)和9.4×10⁵(W)。对于铜绿假单胞菌,存活的CFU数量分别为4.5×10⁶(L)和3.8×10⁶(W)。添加金黄色葡萄球菌后,测量到的峰值分别为37800(L)和35500(W)计数/10⁵个细胞。铜绿假单胞菌的相应值分别为28900(L)和33100计数/10⁵个细胞(W)。添加热灭活血清后,对于金黄色葡萄球菌,实验室菌株的吞噬量从1.07增加到1.94,野生型菌株的吞噬量从0.94增加到2.41个细菌/粒细胞。新鲜血清使吞噬量进一步增加到5.52(L)和4.82(W)。对于铜绿假单胞菌,观察到0.75(L)和0.69(W)个吞噬细菌/粒细胞;添加血清未能带来任何增加。与葡萄球菌不同,假单胞菌仅以点状方式附着在粒细胞膜上。未观察到吞噬差异。