Zeck R, Solliday N, Kehoe T, Berlin B
Am Rev Respir Dis. 1976 Dec;114(6):1061-7. doi: 10.1164/arrd.1976.114.6.1061.
Twenty-one healthy, middle-aged volunteers and 8 patients with chronic lung disease were given live, attenuated influenza virus vaccine by nasal spray. Forced vital capacity, 1-sec forced expiratory volume, ratio of 1-sec forced expiratory volume to forced vital capacity, residual volume, ratio of airway conductance to lung volume, maximal expiratory flows after exhalation of 50 and of 75 per cent of the forced vital capacity, closing volume, slope of Phase III, volume of isoflow, single-breath diffusing capacity for CO, and arterial blood gases were measured before and 3, 7, 10, and 21 days after exposure. Vaccination was well tolerated by the healthy volunteers without change in pulmonary function. In contrast, the patients tended to develop increased respiratory symptoms and had a slight decrease in mean forced expiratory volume in 1 sec 3 weeks after vaccination.
21名健康的中年志愿者和8名慢性肺病患者通过鼻喷雾接种了减毒活流感病毒疫苗。在接种前以及接种后3天、7天、10天和21天测量了用力肺活量、1秒用力呼气量、1秒用力呼气量与用力肺活量的比值、残气量、气道传导率与肺容积的比值、呼出用力肺活量的50%和75%后的最大呼气流量、闭合气量、III期斜率、等流量容积、单次呼吸一氧化碳弥散量以及动脉血气。健康志愿者对疫苗耐受性良好,肺功能无变化。相比之下,患者在接种疫苗3周后往往会出现更多的呼吸道症状,且1秒用力呼气量均值略有下降。