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合成疟疾疫苗SPf66在大型现场试验中的安全性和免疫原性。

Safety and immunogenicity of the synthetic malaria vaccine SPf66 in a large field trial.

作者信息

Amador R, Moreno A, Murillo L A, Sierra O, Saavedra D, Rojas M, Mora A L, Rocha C L, Alvarado F, Falla J C

机构信息

Instituto de Inmunología, Hospital San Juan de Dios, Universidad Nacional de Colombia, Bogotá.

出版信息

J Infect Dis. 1992 Jul;166(1):139-44. doi: 10.1093/infdis/166.1.139.

Abstract

In the first field trial with synthetic malaria vaccine SPf66 in a large population naturally exposed to malaria, 9957 persons greater than 1 year old and residing on the Colombian Pacific coast received three doses of the vaccine. To evaluate vaccine safety, clinical observations were made 30 min and 48 h after each immunization. There were no adverse reactions in 95.7% of cases. In the 4.3% of cases with adverse reactions, local induration and erythema were the most frequent. In a randomly selected group of vaccinees, anti-SPf66 antibody titers were measured after the third dose: 93% of the vaccinees raised antibodies to SPf66. Among these, 55% had titers greater than 1:1600. These results demonstrate the safety and immunogenicity of the SPf66 vaccine in a large field trial.

摘要

在首次针对合成疟疾疫苗SPf66的大规模人群现场试验中,9957名年龄超过1岁且居住在哥伦比亚太平洋沿岸、自然暴露于疟疾环境下的人接种了三剂该疫苗。为评估疫苗安全性,每次免疫后30分钟和48小时进行了临床观察。95.7%的病例未出现不良反应。在4.3%出现不良反应的病例中,局部硬结和红斑最为常见。在一组随机挑选的疫苗接种者中,第三剂接种后检测了抗SPf66抗体滴度:93%的疫苗接种者产生了针对SPf66的抗体。其中,55%的抗体滴度大于1:1600。这些结果证明了SPf66疫苗在大规模现场试验中的安全性和免疫原性。

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