Jerrells T R, Osterman J V
Infect Immun. 1982 Jan;35(1):117-23. doi: 10.1128/iai.35.1.117-123.1982.
Delayed-type hypersensitivity responses of inbred mice during the course of lethal and chronic infections with strains of Rickettsia tsutsugamushi were evaluated by using the influx of radiolabeled cells into antigen-injected ears. Congenic strains of C3H mice, which previously have been shown to be resistant (C3H/RV) or sensitive (C3H/HeDub) to lethal intraperitoneal infection with the Gilliam strain of rickettsiae, both expressed delayed-type hypersensitivity early in the course of infection (5 to 7 days). The sensitive C3H/HeDub mice, however, exhibited a marked decline in reactivity just before death. In contrast, reactivity of C3H/RV mice remained high through day 9 and declined slowly through day 15 after infection. Similar results were obtained when BALB/c mice were infected with either the Karp or the Gilliam strain of rickettsiae, which produce a lethal or nonlethal infection, respectively, in this strain of mice. Rechallenge of C3H/RV mice elicited a rapid increase in reactivity, suggesting a secondary memory response. To analyze delayed-type hypersensitivity during chronic infection, C3H/HeDub mice were immunized by subcutaneous infection with the Gilliam strain of R. tsutsugamushi, and both delayed-type hypersensitivity reactivity and resistance to intraperitoneal challenge were examined. Delayed-type hypersensitivity reactivity developed slowly and peaked at 21 days postimmunization, which correlated with resistance to intraperitoneal challenge. Delayed-type hypersensitivity reactivity declined thereafter, but resistance to intraperitoneal challenge remained through 28 days postimmunization. Delayed-type hypersensitivity reactivity increased after secondary challenge at 28 days, again suggesting antigen memory generated by primary immunization. Transfer of delayed-type hypersensitivity reactivity was accomplished by using immune thymus-derived splenic lymphocytes isolated with nylon-wool columns. Abrogation of the ability of immune spleen cells to transfer delayed-type hypersensitivity reactivity after treatment with anti-Thy 1.2 alloantiserum and complement further supported the view that delayed-type hypersensitivity responses to scrub typhus rickettsiae were mediated by thymus-derived lymphocytes.
通过检测放射性标记细胞向注射抗原耳部的流入情况,评估了不同品系的日本立克次体在致死性和慢性感染过程中近交系小鼠的迟发型超敏反应。先前已证明对立克次体吉列姆株致死性腹腔感染具有抗性(C3H/RV)或敏感性(C3H/HeDub)的C3H小鼠同基因品系,在感染过程早期(5至7天)均表现出迟发型超敏反应。然而,敏感的C3H/HeDub小鼠在死亡前反应性显著下降。相比之下,C3H/RV小鼠的反应性在感染后第9天前一直很高,并在感染后第15天缓慢下降。当BALB/c小鼠分别感染立克次体卡尔普株或吉列姆株时,也得到了类似结果,这两种菌株在该品系小鼠中分别产生致死性或非致死性感染。对C3H/RV小鼠再次攻击引发反应性迅速增加,表明存在二次记忆反应。为了分析慢性感染期间的迟发型超敏反应,用日本立克次体吉列姆株皮下感染C3H/HeDub小鼠进行免疫,并检测迟发型超敏反应性和对腹腔攻击的抵抗力。迟发型超敏反应性发展缓慢,在免疫后21天达到峰值,这与对腹腔攻击的抵抗力相关。此后迟发型超敏反应性下降,但对腹腔攻击的抵抗力在免疫后28天内仍然存在。在28天进行二次攻击后迟发型超敏反应性增加,再次表明初次免疫产生了抗原记忆。通过使用用尼龙毛柱分离的免疫胸腺来源的脾淋巴细胞实现迟发型超敏反应性的转移。用抗Thy 1.2同种异体抗血清和补体处理后,免疫脾细胞转移迟发型超敏反应性的能力被消除,这进一步支持了对恙虫病立克次体的迟发型超敏反应由胸腺来源的淋巴细胞介导的观点。