Ricci Maria Luisa, Torosantucci Antonella, Scaturro Maria, Chiani Paola, Baldassarri Lucilla, Pastoris Maddalena Castellani
Department of Infectious, Parasitic and Immune-Mediated Diseases, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Roma, Italy.
Vaccine. 2005 Sep 23;23(40):4811-20. doi: 10.1016/j.vaccine.2005.05.013.
The capacity of a purified preparation of Legionella pneumophila flagella (FLA) to induce protective immune responses was studied in an A/J mouse model. Animals immunized with FLA promptly mounted an anti-FLA antibody response and also developed a strong activation of both innate and adaptive cell-mediated immunity, as shown by an early release of pro-inflammatory cytokines in the peritoneal cavity, and by a positive cutaneous delayed-type hypersensitivity reaction and in vitro splenic lymphocyte proliferation in response to FLA antigens. Mice treated with FLA either i.v. or i.p. also survived (100% rate) a lethal i.p. challenge with L. pneumophila. Protection induced by FLA lasted for at least 30 days after treatment, but less than 60, and was effective against the challenge with different serogroups of L. pneumophila. Resistance conferred by FLA immunization could be partially transferred to naïve animals by the adoptive transfer of immune splenocytes but not by passive immunization with anti-FLA iperimmune sera. The capacity to induce protective immunity was specifically attributable to flagellar components, as demonstrated by the lack of protection in mice immunized with a sham flagella preparation from a non-flagellated bacterial strain or with protease-digested FLA. In addition, heat-denatured FLA was inactive, suggesting loss of immunogenicity following denaturation. The present study provides evidence that L. pneumophila flagellum is strongly immunogenic and capable to stimulate, without adjuvants, early natural and acquired, T-cell-mediated immune responses and to induce significant protection against a lethal bacterial challenge in A/J mice. Antigenic characterization of this bacterial organelle and elucidation of mechanisms underlying flagella-induced protection would be of great value in understanding the immunopathogenesis of the disease and in developing possible therapeutic strategies for human legionellosis.
在A/J小鼠模型中研究了嗜肺军团菌鞭毛(FLA)纯化制剂诱导保护性免疫反应的能力。用FLA免疫的动物迅速产生抗FLA抗体反应,并且先天和适应性细胞介导的免疫也强烈激活,这表现为腹腔中促炎细胞因子的早期释放、阳性皮肤迟发型超敏反应以及体外脾淋巴细胞对FLA抗原的增殖反应。经静脉内或腹腔内给予FLA治疗的小鼠在接受嗜肺军团菌致死性腹腔攻击后也存活(存活率100%)。FLA诱导的保护作用在治疗后持续至少30天,但不到60天,并且对不同血清群的嗜肺军团菌攻击有效。通过免疫脾细胞的过继转移,FLA免疫赋予的抗性可部分转移至未免疫动物,但用抗FLA超免疫血清进行被动免疫则不能。诱导保护性免疫的能力具体归因于鞭毛成分,这通过用来自无鞭毛细菌菌株的假鞭毛制剂或经蛋白酶消化的FLA免疫的小鼠缺乏保护作用得以证明。此外,热变性的FLA无活性,表明变性后免疫原性丧失。本研究提供了证据,表明嗜肺军团菌鞭毛具有强免疫原性,能够在无佐剂的情况下刺激早期天然和获得性T细胞介导的免疫反应,并在A/J小鼠中诱导对致死性细菌攻击的显著保护作用。对这种细菌细胞器的抗原特性进行表征以及阐明鞭毛诱导保护的潜在机制,对于理解该疾病的免疫发病机制以及开发可能的人类军团病治疗策略具有重要价值。