Titus R G, Marchand M, Boon T, Louis J A
Parasite Immunol. 1985 Sep;7(5):545-55. doi: 10.1111/j.1365-3024.1985.tb00098.x.
A limiting dilution assay for the quantification of Leishmania major in infected mouse tissue was developed. The assay was found to be both sensitive and reliable, and, due to its design, could be scored either visually or following the incorporation of 3H-thymidine by the growing parasites. Results are presented in which the assay was employed to enumerate L. major in the tissues of susceptible (BALB/c) and resistant (CBA) mice at intervals after infection with L. major. It was found that parasites could be detected at the site of injection with L. major as early as 3 days after infection. By day 8, a substantial increase in the number of parasites at the lesion site had occurred in both strains of mice. Subsequently, whereas the number of parasites decreased in the lesions of CBA mice, their number steadily increased in the lesions of BALB/c mice. Parasites were detected in lymph nodes draining the lesion site in both BALB/c and CBA mice by 28 days after infection. Interestingly, a low number of L. major was found in the lymph nodes of CBA mice at 100 days after infection, a time when no parasites could be detected at the lesion site. Previous results from this laboratory have demonstrated that the adoptive transfer of L. major-specific L3T4-positive T-cell populations exacerbated cutaneous lesions induced by L. major in BALB/c mice. Experiments presented here indicate that the adoptive transfer of L. major-specific T-cells also exacerbated cutaneous leishmaniasis in CBA mice. Using the sensitive limiting dilution assay presently described, it was found that this unexpected exacerbative effect of L. major-specific T-cells on lesion development was accompanied by a substantial increase in the number of parasites in the lesions of the adoptively transferred mice.
我们开发了一种用于定量感染小鼠组织中硕大利什曼原虫的有限稀释分析方法。该分析方法被证明既灵敏又可靠,并且由于其设计,可以通过肉眼评分,也可以在生长的寄生虫掺入3H-胸腺嘧啶后进行评分。本文给出了相关结果,其中该分析方法被用于在感染硕大利什曼原虫后的不同时间点,对易感(BALB/c)和抗性(CBA)小鼠组织中的硕大利什曼原虫进行计数。结果发现,在感染硕大利什曼原虫后3天,最早可在注射部位检测到寄生虫。到第8天,两种品系小鼠病变部位的寄生虫数量都有大幅增加。随后,CBA小鼠病变部位的寄生虫数量减少,而BALB/c小鼠病变部位的寄生虫数量则稳步增加。感染后28天,在BALB/c和CBA小鼠病变部位引流的淋巴结中均检测到寄生虫。有趣的是,在感染后100天,CBA小鼠的淋巴结中发现少量硕大利什曼原虫,此时在病变部位未检测到寄生虫。该实验室之前的结果表明,将硕大利什曼原虫特异性L3T4阳性T细胞群体进行过继转移会加剧BALB/c小鼠由硕大利什曼原虫诱导的皮肤病变。本文呈现的实验表明,将硕大利什曼原虫特异性T细胞进行过继转移也会加剧CBA小鼠的皮肤利什曼病。使用目前所描述的灵敏的有限稀释分析方法,发现硕大利什曼原虫特异性T细胞对病变发展的这种意外的加剧作用伴随着过继转移小鼠病变部位寄生虫数量的大幅增加。