Geme J W, Yamauchi T, Eisenklam E J, Noren G R, Aase J M, Jurmain R B, Henn R M, Gabel M C, Hollister A W, Paumier R
Am J Epidemiol. 1975 Mar;101(3):253-63. doi: 10.1093/oxfordjournals.aje.a112093.
The biologic validity of cell-mediated immunity to mumps virus was evaluated in 395 children, adolescents and adults. The study protocol included the determination of cutaneous delayed hypersensitivity to viral and avian control antigens and in 79% of the subjects an essential double bleeding was performed before and after mumps virus skin test for assay of neutralizing antibody. Seven per cent of subjects expressed sufficient delayed hypersentitivity to the control antigen to erase an apparently positive mumps virus skin test. Anamnestic conversions from seronegativity to seropositivity, elicited by the mumps virus skin test, increased from 4% in children to 25% in adults, which suggests waning B-cell recognition of prior mumps virus infection in adults. Although pregnancy diminished the difference (p smaller than .001), adults showed greater cutaneous delayed hypersensitivity to mumps virus antigen than did children (p smaller than .001), suggesting that mumps virus reinfection or persistence induced the escalation of more sensitive T-cell recognition with increasing age. Humoral immunity, assessed by the double bleeding technique in the vast majority of individuals, rose form 16% (1-4 years), 45% (5-9 years) and 80% (10-14 years) to 94% in adolescents and adults. Ordinarily 75-95% in other age groups, the decline of correlation between mumps virus cellular and humoral immunity to 60% in school children may result from prior parainfluenza virus infection, inconsistent potency of the skin test antigen, concurrent immunosuppressive infection, and lagging induction of mumps virus cellular immunity in recently infected individuals. Immunologic study of a large colony of subhuman primates failed to establish an hierarchial antigenic interrelationship among mumps virus and two additional paramyxoviruses.
对395名儿童、青少年和成人评估了针对腮腺炎病毒的细胞介导免疫的生物学有效性。研究方案包括测定对病毒和禽类对照抗原的皮肤迟发型超敏反应,并且在79%的受试者中,在腮腺炎病毒皮肤试验前后进行了一次必要的二次采血,以检测中和抗体。7%的受试者对对照抗原表现出足够的迟发型超敏反应,从而消除了明显阳性的腮腺炎病毒皮肤试验结果。由腮腺炎病毒皮肤试验引发的从血清阴性到血清阳性的回忆性转变,在儿童中从4%增加到成人中的25%,这表明成人中B细胞对既往腮腺炎病毒感染的识别能力在下降。尽管妊娠缩小了这种差异(p小于0.001),但成人对腮腺炎病毒抗原的皮肤迟发型超敏反应比儿童更强(p小于0.001),这表明腮腺炎病毒再感染或持续感染随着年龄增长诱导了更敏感的T细胞识别能力的增强。通过二次采血技术在绝大多数个体中评估的体液免疫,从16%(1 - 4岁)、45%(5 - 9岁)和80%(10 - 14岁)上升到青少年和成人中的94%。在其他年龄组中通常为75 - 95%,学龄儿童中腮腺炎病毒细胞免疫与体液免疫之间的相关性下降至60%,可能是由于既往副流感病毒感染、皮肤试验抗原效价不一致、并发免疫抑制性感染以及近期感染个体中腮腺炎病毒细胞免疫诱导滞后所致。对一大群亚人类灵长类动物的免疫学研究未能确定腮腺炎病毒与另外两种副粘病毒之间的等级抗原相互关系。