Locher C P, Blackbourn D J, Barnett S W, Murthy K K, Cobb E K, Rouse S, Greco G, Reyes-Terán G, Brasky K M, Carey K D, Levy J A
Department of Medicine, University of California, San Francisco 94143-1270, USA.
J Infect Dis. 1997 Oct;176(4):948-59. doi: 10.1086/516544.
An animal model was used to assess whether resistance to superinfection by human immunodeficiency virus (HIV) can exist in vivo. Asymptomatic baboons (Papio cynocephalus), previously infected with HIV-2, were first challenged with homologous virus (HIV-2UC2 or HIV-2UC14) and later with heterologous virus (HIV-2UC12). After both virus inoculations, either resistance to viral infection or a transient viremia was observed. The original virus was recovered in 3 baboons, suggesting that reactivation of a latent infection occurred on heterologous challenge and that HIV-2 superinfection is blocked by processes established during prior infection. Antibody titers measured by ELISA and virus neutralization remained at low levels. However, suppression of HIV-1 replication was observed with CD8 T cells and filtered cell culture supernatants. The soluble factor involved was not a beta-chemokine. This resistance to HIV superinfection appears to be mediated at least in part by CD8 T cells that suppress virus production.
利用动物模型评估体内是否存在对人类免疫缺陷病毒(HIV)重复感染的抗性。将先前感染HIV-2的无症状狒狒(豚尾狒狒)先用同源病毒(HIV-2UC2或HIV-2UC14)攻击,随后用异源病毒(HIV-2UC12)攻击。在两次病毒接种后,观察到要么对病毒感染有抗性,要么出现短暂病毒血症。在3只狒狒中检测到了原始病毒,这表明在异源攻击时发生了潜伏感染的重新激活,并且HIV-2重复感染被先前感染期间建立的过程所阻断。通过ELISA和病毒中和检测的抗体滴度维持在低水平。然而,在CD8 T细胞和过滤后的细胞培养上清液中观察到了HIV-1复制的抑制。所涉及的可溶性因子不是β趋化因子。这种对HIV重复感染的抗性似乎至少部分是由抑制病毒产生的CD8 T细胞介导的。