Onanga Richard, Souquière Sandrine, Makuwa Maria, Mouinga-Ondeme Augustin, Simon François, Apetrei Cristian, Roques Pierre
Département de Virologie, Centre International de Recherche Médicales, Gabon.
J Virol. 2006 Apr;80(7):3301-9. doi: 10.1128/JVI.80.7.3301-3309.2006.
Mandrills are the only nonhuman primate (NHP) naturally infected by two types of simian immunodeficiency virus (SIV): SIVmnd-1 and SIVmnd-2. We have already reported that the high SIVmnd-1 replication during primary infection contrasts with only transient changes in CD4+ and CD8+ cell counts. Since early virus-host interactions predict viral control and disease progression in human immunodeficiency virus-infected patients, we investigated the dynamics of SIVmnd-2 primary infection in mandrills to examine the impact on immune effectors in blood and lymph nodes (LNs). To avoid in vitro strain selection, all mandrills in this study received plasma from SIVmnd-2-infected mandrills. SIVmnd-2 plasma viremia peaked at 10(7) to 10(8) RNA copies/ml between days 7 and 10. This peak was followed in all four monkeys by a decline in virus replication, with a set point level of 10(5) to 10(6) RNA copies/ml at day 42 postinfection (p.i.). Viral DNA load in PBMC and LNs also peaked between days 7 and 10 (10(5) to 10(6) DNA copies/10(6) cells) and stabilized at 10(3) to 10(4) DNA copies/10(6) cells during the chronic phase. Anti-SIVmnd-2 antibodies were detected starting from days 28 to 32. A transitory decline of CD3+ CD4+ cells in the LNs occurred in animals with high peak VLs. CD4+ and CD8+ T-cell activation in blood and LNs was noted between days 5 and 17 p.i., surrounding the peak of viral replication. This was most significant in the LNs. Activation markers then returned to preinfection values despite continuous and active viral replication during the chronic infection. The dynamics of SIVmnd-2 infection in mandrills showed a pattern similar to that of SIVmnd-1 infection. This might be a general feature of nonpathogenic SIV natural African NHP models.
山魈是唯一自然感染两种猿猴免疫缺陷病毒(SIV)的非人灵长类动物(NHP):SIVmnd - 1和SIVmnd - 2。我们已经报道过,初次感染期间SIVmnd - 1的高复制与CD4 +和CD8 +细胞计数仅短暂变化形成对比。由于早期病毒与宿主的相互作用可预测人类免疫缺陷病毒感染患者的病毒控制和疾病进展,我们研究了山魈中SIVmnd - 2初次感染的动态变化,以检查其对血液和淋巴结(LN)中免疫效应细胞的影响。为避免体外毒株选择,本研究中的所有山魈均接受来自感染SIVmnd - 2的山魈的血浆。SIVmnd - 2血浆病毒血症在第7天至第10天达到峰值,为10(7)至10(8)RNA拷贝/毫升。在所有四只猴子中,此峰值之后病毒复制下降,在感染后(p.i.)第42天的设定点水平为10(5)至10(6)RNA拷贝/毫升。外周血单核细胞(PBMC)和淋巴结中的病毒DNA载量也在第7天至第10天达到峰值(10(5)至10(6)DNA拷贝/10(6)个细胞),并在慢性期稳定在10(3)至10(4)DNA拷贝/10(6)个细胞。从第28天至第32天开始检测到抗SIVmnd - 2抗体。在病毒载量峰值高的动物中,淋巴结中的CD3 + CD4 +细胞出现短暂下降。在感染后第5天至第17天,血液和淋巴结中出现CD4 +和CD8 + T细胞活化,围绕病毒复制峰值。这在淋巴结中最为显著。尽管在慢性感染期间病毒持续活跃复制,但活化标志物随后恢复到感染前的值。山魈中SIVmnd - 2感染的动态变化显示出与SIVmnd - 1感染相似的模式。这可能是非致病性SIV自然非洲NHP模型的一个普遍特征。