Del Gobbo V, Villani N, Balestra E, Marini S, Firriolo A, Caliò R
Boll Ist Sieroter Milan. 1987;66(1):1-8.
T-lymphocyte blastogenic response to Concanavalin A, interleukin-2 (IL-2) production and NK cell activity were studied in three groups of Balb/c mice infected with intranasal inoculum of A/Chile/1/83 (H1N1) influenza virus, vaccinated with same virus glycoproteins and infected fifteen day after vaccination. Virus infection results in T-cell function impairment. In fact T-cell blastogenic response and IL-2 production are profoundly decreased as early as 24 hours, whereas NK cell activity is depressed only later. Instead viral glycoprotein vaccination induces an enhancement of CMI related parameters and protects the host from virus immunosuppressive effects.
在三组经鼻接种A/智利/1/83(H1N1)流感病毒、用相同病毒糖蛋白进行疫苗接种并在接种后15天感染的Balb/c小鼠中,研究了T淋巴细胞对刀豆球蛋白A的增殖反应、白细胞介素-2(IL-2)的产生和自然杀伤(NK)细胞活性。病毒感染导致T细胞功能受损。事实上,早在24小时时T细胞增殖反应和IL-2的产生就已显著降低,而NK细胞活性仅在之后才受到抑制。相反,病毒糖蛋白疫苗接种可诱导细胞介导免疫(CMI)相关参数增强,并保护宿主免受病毒免疫抑制作用的影响。