Priebe Gregory P, Meluleni Gloria J, Coleman Fadie T, Goldberg Joanna B, Pier Gerald B
Channing Laboratory, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Infect Immun. 2003 Mar;71(3):1453-61. doi: 10.1128/IAI.71.3.1453-1461.2003.
Studies of immunity to Pseudomonas aeruginosa have indicated that a variety of potential immunogens can elicit protection in animal models, utilizing both antibody- and cell-mediated immune effectors for protection. To attempt to optimize delivery of multiple protective antigens and elicit a broad range of immune effectors, we produced an aroA deletion mutant of the P. aeruginosa serogroup O2/O5 strain PAO1, designated PAO1deltaaroA. Previously, we reported that this strain elicits high levels of opsonic antibody directed against many serogroup O2/O5 strains after nasal immunization of mice and rabbits. Here, we assessed the protective efficacy of immunization with PAO1deltaaroA against acute fatal pneumonia in mice. After active immunization, high levels of protection were achieved against an ExoU-expressing cytotoxic variant of the parental strain PAO1 at doses up to 1,000-fold greater than the 50% lethal dose. Significant protection against PAO1 and two of four other serogroup O2/O5 strains was also found, but there was no protection against serogroup-heterologous strains. The serogroup O2/O5 strains not protected against were killed in opsonophagocytic assays as efficiently as the strains with which protection was seen, indicating a lack of correlation of protection and opsonic killing within the serogroup. In passive immunization experiments using challenge with wild-type PAO1 or other noncytotoxic members of the O2/O5 serogroup, there was no protection despite the presence of high levels of opsonic antibody in the mouse sera. However, passive immunization did prevent mortality from pneumonia due to the cytotoxic PAO1 variant at low-challenge doses. These data suggest that a combination of humoral and cellular immunity is required for protection against P. aeruginosa lung infections, that such immunity can be elicited by using aroA deletion mutants, and that a multivalent P. aeruginosa vaccine composed of aroA deletion mutants of multiple serogroups holds significant promise.
针对铜绿假单胞菌的免疫研究表明,多种潜在免疫原可在动物模型中引发保护作用,利用抗体介导和细胞介导的免疫效应因子实现保护。为了尝试优化多种保护性抗原的递送并引发广泛的免疫效应因子,我们构建了铜绿假单胞菌血清型O2/O5菌株PAO1的aroA缺失突变体,命名为PAO1deltaaroA。此前,我们报道该菌株在对小鼠和兔子进行鼻腔免疫后,可引发针对许多血清型O2/O5菌株的高水平调理抗体。在此,我们评估了用PAO1deltaaroA免疫对小鼠急性致命性肺炎的保护效果。主动免疫后,在剂量高达比50%致死剂量大1000倍的情况下,对亲本菌株PAO1的表达ExoU的细胞毒性变体实现了高水平的保护。还发现对PAO1以及其他四个血清型O2/O5菌株中的两个有显著保护作用,但对血清型异源菌株没有保护作用。未受到保护的血清型O2/O5菌株在调理吞噬试验中与受到保护的菌株一样有效地被杀死,这表明血清型内保护与调理杀伤之间缺乏相关性。在使用野生型PAO1或O2/O5血清型的其他非细胞毒性成员进行攻击的被动免疫实验中,尽管小鼠血清中存在高水平的调理抗体,但没有保护作用。然而,被动免疫确实在低攻击剂量下预防了由细胞毒性PAO1变体引起的肺炎死亡。这些数据表明,针对铜绿假单胞菌肺部感染的保护需要体液免疫和细胞免疫的联合作用,这种免疫可以通过使用aroA缺失突变体来引发,并且由多个血清型的aroA缺失突变体组成的多价铜绿假单胞菌疫苗具有很大的前景。