Brass C, Stevens D A
Infect Immun. 1982 Apr;36(1):387-95. doi: 10.1128/iai.36.1.387-395.1982.
Marked resistance of 9-week-old mice as compared to that of 5-week-old mice was demonstrated after pulmonary challenge with three strains of Blastomyces dermatitidis of various virulences. Quantitative studies with graded doses of the strain that was intermediate in virulence indicated that the difference in resistance between the two age groups was 1,000-fold. Acquisition of resistance appeared to be gradual between the ages of 5 and 9 weeks. Maturational differences among individual mice appeared to be most crucial at 5 weeks of age. With two fungal strains, susceptibility of the younger mice was also demonstrated after intraperitoneal challenge; with one of these strains, the differences between the two groups of mice were much smaller, suggesting that maturation of defenses in the peritoneal cavity may develop faster. Studies with serial sacrifice of different groups of mice given pulmonary challenges (of comparable amounts) indicated that the differences are not due to the amount of challenge reaching the lungs or its clearance. The infection-limiting effect in the lungs of older mice occurred within 4 days after challenge. These differences in resistance over this narrow age interval appear to be unique; resistance appears to occur later than resistance to other infectious agents and at a time when most murine immune functions have matured. This model and these observations provide an opportunity for further studies of the mechanism of resistance and are relevant to clinical observations of susceptibility of infants and children to deep mycoses.
在用三种不同毒力的皮炎芽生菌菌株对肺部进行攻击后,结果显示9周龄小鼠比5周龄小鼠具有明显更强的抵抗力。对中等毒力菌株进行分级剂量的定量研究表明,两个年龄组之间的抵抗力差异为1000倍。在5至9周龄之间,抵抗力的获得似乎是逐渐发生的。个体小鼠之间的成熟差异在5周龄时似乎最为关键。对于两种真菌菌株,腹腔注射攻击后也显示出幼龄小鼠更易感染;对于其中一种菌株,两组小鼠之间的差异要小得多,这表明腹腔防御的成熟可能发展得更快。对接受肺部攻击(等量)的不同组小鼠进行连续处死的研究表明,差异并非由于到达肺部的攻击量或其清除情况所致。老龄小鼠肺部的感染限制作用在攻击后4天内就会出现。在这个狭窄年龄区间内抵抗力的这些差异似乎是独特的;抵抗力出现的时间似乎比抵抗其他感染因子的时间要晚,而且是在大多数小鼠免疫功能已经成熟的时候。这个模型和这些观察结果为进一步研究抵抗力的机制提供了机会,并且与婴儿和儿童对深部真菌病易感性的临床观察相关。