Kasper D L, Finberg R F, Crabb J, Onderdonk A B
Channing Laboratory, Brigham and Women's Hospital, Boston, Massachusetts.
Scand J Infect Dis Suppl. 1989;62:29-34.
Bacteroides fragilis is the most commonly isolated anaerobe from intraabdominal infections. In experimental models of intraabdominal sepsis, B. fragilis has been shown to be uniquely virulent. Some of these virulence traits are due to the capsular polysaccharide of this organism. Immunity to infection secondary to B. fragilis seems to involve both arms of the immune system. Humoral immunity (complement, antibody and PMNs) is critical to clearance of these bacteria from the blood stream. Cellular immune mechanisms predominate against intraabdominal abscess formation. Adoptive transfer experiments have shown that a CD8+, IJ+, non H2 restricted immune T cell or lysate from this T cell confers protection to immunocompetent, naive mice. An in vivo system has been developed to begin defining the mechanism of protection. B. fragilis placed inside a filter containment chamber within the peritoneum of immune mice are specifically killed over an 8-day period in the absence of white blood cells. This killing phenomenon was also observed inside filter chambers within mice receiving adoptively transferred immune T cells or lysates of these T cells. Furthermore, killing is specific to B. fragilis. These results support a T cell dependent mechanism for killing this bacteria and provide an interesting model for further exploration.
脆弱拟杆菌是腹腔感染中最常分离出的厌氧菌。在腹腔脓毒症的实验模型中,脆弱拟杆菌已被证明具有独特的毒力。其中一些毒力特性归因于该生物体的荚膜多糖。对脆弱拟杆菌继发感染的免疫似乎涉及免疫系统的两个分支。体液免疫(补体、抗体和中性粒细胞)对于从血流中清除这些细菌至关重要。细胞免疫机制在抵抗腹腔脓肿形成方面占主导地位。过继转移实验表明,CD8 +、IJ +、非H2限制的免疫T细胞或该T细胞的裂解物能为具有免疫能力的未接触过抗原的小鼠提供保护。已开发出一种体内系统来开始确定保护机制。置于免疫小鼠腹膜内滤器容纳腔内的脆弱拟杆菌在无白细胞的情况下,在8天内被特异性杀灭。在接受过继转移免疫T细胞或这些T细胞裂解物的小鼠的滤器腔内也观察到了这种杀伤现象。此外,杀伤作用对脆弱拟杆菌具有特异性。这些结果支持一种依赖T细胞的杀灭这种细菌的机制,并为进一步探索提供了一个有趣的模型。