Geginat G, Kretschmar M, Walter S, Junker D, Hof H, Nichterlein T
Institut für Medizinische Mikrobiologie und Hygiene, Fakultät für Klinische Medizin Mannheim der Universität Heidelberg, 68167 Mannheim, Germany.
J Infect Dis. 1999 Oct;180(4):1186-94. doi: 10.1086/315007.
Amphotericin B is frequently used for the treatment of fungal infections of immunocompromised individuals. Whereas immunomodulatory side effects of this agent are known, the influence of amphotericin B was studied in the model of murine Listeria monocytogenes infection. Treatment of L. monocytogenes-immune mice with a nontoxic dose of amphotericin B (0.75 mg/kg) reduced antilisterial protection by 4-5 orders of magnitude, while it had no significant effect on natural immunity against L. monocytogenes in naive mice. Treatment of mice with amphotericin B also abolished the protection mediated by transfer of an L. monocytogenes-specific CD8 T cell line. Furthermore, in vitro analysis showed that amphotericin B impaired target cell lysis and interferon-gamma production by peptide-specific CD8 T cell lines and antigen presentation by L. monocytogenes-infected macrophagelike cells. These data indicate that amphotericin B has a strong suppressive effect on the function of CD8 T cells in vitro and in vivo.
两性霉素B常用于治疗免疫功能低下个体的真菌感染。虽然已知该药物具有免疫调节副作用,但在小鼠单核细胞增多性李斯特菌感染模型中研究了两性霉素B的影响。用无毒剂量的两性霉素B(0.75mg/kg)治疗单核细胞增多性李斯特菌免疫的小鼠,使抗李斯特菌保护作用降低了4至5个数量级,而对未感染小鼠针对单核细胞增多性李斯特菌的天然免疫没有显著影响。用两性霉素B治疗小鼠也消除了由单核细胞增多性李斯特菌特异性CD8 T细胞系转移介导的保护作用。此外,体外分析表明,两性霉素B损害了肽特异性CD8 T细胞系的靶细胞裂解和干扰素-γ产生,以及单核细胞增多性李斯特菌感染的巨噬样细胞的抗原呈递。这些数据表明,两性霉素B在体外和体内对CD8 T细胞功能具有强烈的抑制作用。