Hayden F G, Winther B, Donowitz G R, Mills S E, Innes D J
J Infect Dis. 1987 Jul;156(1):64-72. doi: 10.1093/infdis/156.1.64.
Healthy adults were randomly assigned to receive intranasal sprays of recombinant leukocyte A interferon (IFN; 9 X 10(6) U per day) or placebo once daily for four or 10 days. Scrape nasal biopsy specimens stained by hematoxylin and eosin and mucosal punch biopsy specimens stained by immunoperoxidase techniques with monoclonal antibodies to lymphocyte subsets were collected before and after exposure. Blinded analysis of the punch biopsy specimens by two pathologists found increased degrees of lymphocyte infiltration compared with preexposure samples in 56% of IFN vs. 0% of placebo recipients at four days (P = .008) and 60% of IFN vs. 10% of placebo recipients at 10 days (P = .057). By immunoperoxidase staining the cellular infiltrates were primarily in the subepithelium and comprised principally (mean, greater than or equal to 84%) T lymphocytes. In the 10-day IFN recipients, subepithelial T helper (Leu-3):T suppressor (Leu-2) cell ratios ranged from 2:1 to 5:1. The number of distribution of B (Leu-14) or natural killer (Leu-7) cells did not appear affected by IFN.
健康成年人被随机分配,每天接受一次重组白细胞A干扰素(IFN;每天9×10⁶单位)或安慰剂的鼻内喷雾,持续4天或10天。在暴露前后收集经苏木精和伊红染色的刮取鼻活检标本以及用针对淋巴细胞亚群的单克隆抗体通过免疫过氧化物酶技术染色的黏膜穿孔活检标本。两名病理学家对穿孔活检标本进行盲法分析发现,4天时,56%接受IFN的受试者与0%接受安慰剂的受试者相比,淋巴细胞浸润程度增加(P = .008);10天时,60%接受IFN的受试者与10%接受安慰剂的受试者相比,淋巴细胞浸润程度增加(P = .057)。通过免疫过氧化物酶染色,细胞浸润主要位于上皮下,主要由(平均,大于或等于84%)T淋巴细胞组成。在接受10天IFN治疗的受试者中,上皮下辅助性T细胞(Leu - 3):抑制性T细胞(Leu - 2)的比例范围为2:1至5:1。B(Leu - 14)细胞或自然杀伤(Leu - 7)细胞的数量分布似乎未受IFN影响。