Tuffrey M, Falder P, Taylor-Robinson D
Br J Exp Pathol. 1984 Feb;65(1):51-8.
Progesterone-treated CBA mice which had had genital infections with a fast, human strain of Chlamydia trachomatis either 8, 16, 58, or 69 weeks previously were rechallenged through the uterine wall, along with groups of untreated controls. Serum IgG antibody and/or local IgA antibody was measured using a micro-immunofluorescence technique. Although the infection was self-limiting, chlamydiae were cleared significantly more quickly from the previously infected groups than from their controls in all experiments. However, mice which had had a previous infection recently and which had high titres (geometric mean 1: greater than or equal to 2048) of serum IgG antibody and local IgA antibody immediately before rechallenge, were as susceptible as mice which had had a distant past infection and which had much lower titres (geometric mean 1:48) of serum IgG antibody. Thus, some immunity was induced in the mouse model, but pre-existing antibody seemed to be of little importance in this, and did not influence the initial susceptibility to reinfection.
对8周、16周、58周或69周前曾感染过快速生长的人沙眼衣原体菌株且接受过孕酮治疗的CBA小鼠,通过子宫壁进行再次攻击,同时设置未处理的对照组。使用微量免疫荧光技术测量血清IgG抗体和/或局部IgA抗体。尽管感染是自限性的,但在所有实验中,衣原体从先前感染组清除的速度明显快于对照组。然而,近期曾有过感染且在再次攻击前血清IgG抗体和局部IgA抗体滴度较高(几何平均滴度1:大于或等于2048)的小鼠,与过去曾有过遥远感染且血清IgG抗体滴度低得多(几何平均滴度1:48)的小鼠一样易感。因此,在小鼠模型中诱导了一些免疫力,但预先存在的抗体在这方面似乎作用不大,并且不影响对再感染的初始易感性。