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在黑猩猩中对丙型肝炎病毒进行滴定以确定传播所需的拷贝数。

Titration of hepatitis C virus in chimpanzees for determining the copy number required for transmission.

作者信息

Katayama Keiko, Kumagai Junko, Komiya Yutaka, Mizui Masaaki, Yugi Hisao, Kishimoto Shinya, Yamanaka Retsuji, Tamatsukuri Shigeru, Tomoguri Tetsushi, Miyakawa Yuzo, Tanaka Junko, Yoshizawa Hiroshi

机构信息

Department of Infectious Disease and Control, Hiroshima University Graduate School of Biomedical Sciences, Kasumi, Hiroshima, Japan.

出版信息

Intervirology. 2004;47(1):57-64. doi: 10.1159/000076643.

Abstract

OBJECTIVE

To determine the copy number of hepatitis C virus (HCV) RNA, determined by nucleic acid amplification test (NAT) for screening blood units in Japan, that can transmit infection to chimpanzees.

METHODS

Fresh-frozen plasma with markers of HCV infection, as well as inocula pedigreed from 1 of them, were evaluated for the infectious activity in chimpanzees.

RESULTS

One unit each (273-282 ml) of fresh-frozen plasma from 2 blood donors or a pool from 13 donors to make a unit, which contained high-titered antibody to HCV but without HCV RNA detectable by NAT, did not infect any of 3 chimpanzees. Two chimpanzees were infected, however, when they were inoculated with 1 ml of serum from a blood donor in the 'window period' of HCV infection and containing 7.0 x 10(6) copies/ml of HCV RNA. The preacute phase serum from 1 of them harvested 7 weeks after the inoculation was titrated in 2 chimpanzees, and an inoculum containing approximately 2 x 10(1) copies of HCV RNA could transmit infection to both of them.

CONCLUSION

Approximately 20 copies of HCV can transmit infection to recipients, which needs to be taken into consideration in planning the screening of blood units for HCV RNA by NAT. Although the sensitivity of present NAT could be improved further, there would be a limit of it in detecting a low-level HCV RNA in the window period of donors with the infectious capacity in recipients.

摘要

目的

确定在日本用于筛查血液单位的核酸扩增试验(NAT)所测定的丙型肝炎病毒(HCV)RNA的拷贝数,该拷贝数可导致黑猩猩感染。

方法

对具有HCV感染标志物的新鲜冷冻血浆以及从其中一份血浆衍生而来的接种物进行黑猩猩感染活性评估。

结果

来自2名献血者的各1单位(273 - 282毫升)新鲜冷冻血浆,或来自13名献血者混合制成1单位的血浆,其含有高滴度抗HCV抗体但NAT检测不到HCV RNA,未感染3只黑猩猩中的任何一只。然而,当2只黑猩猩接种来自一名处于HCV感染“窗口期”的献血者的1毫升血清(含7.0×10⁶拷贝/毫升HCV RNA)时被感染。其中1只黑猩猩接种后7周采集的急性期前血清在另外2只黑猩猩中进行滴定,含有约2×10¹拷贝HCV RNA的接种物可使它们都被感染。

结论

约20拷贝的HCV可导致受血者感染,这在计划通过NAT筛查血液单位中的HCV RNA时需要考虑。尽管目前NAT的灵敏度可进一步提高,但在检测处于受血者有感染能力的献血者窗口期的低水平HCV RNA时仍存在局限性。

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