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肯尼亚未接受治疗的HIV-1感染儿童的病毒载量、CD4+T淋巴细胞计数及抗体滴度;对免疫缺陷和艾滋病进展的影响

Viral load, CD4+ T-lymphocyte counts and antibody titres in HIV-1 infected untreated children in Kenya; implication for immunodeficiency and AIDS progression.

作者信息

Ochieng Washingtone, Ogoyi Dorington, Mulaa Francis J, Ogola Simon, Musoke Rachel, Otsyula Moses G

机构信息

Centre for Virus Research, Kenya Medical Research Institute, Nairobi, Kenya.

出版信息

Afr Health Sci. 2006 Mar;6(1):3-13. doi: 10.5555/afhs.2006.6.1.3.

Abstract

BACKGROUND

There are limited reports on HIV-1 RNA load, CD4+ T-lymphocytes and antibody responses in relation to disease progression in HIV-1 infected untreated children in Africa.

METHODS

To describe the relationships between these parameters, we conducted a longitudinal cohort study involving 51 perinatally HIV-1 infected children aged between 1 and 13 years. HIV status was determined by ELISA and confirmed by western blot and PCR. Antibodies were quantified by limiting dilution ELISA, plasma HIV-1 RNA load by RT-PCR and CD4+ T-lymphocytes by FACSCount.

RESULTS

Asymptomatic and symptomatic disease had, respectively, a rise in median HIV-1 RNA load from 1,195 to 132,543 and from 42,962 to 1,109,281 copies/ml in children below 6 years. The increase in viral load was 10-fold higher for asymptomatic compared to other categories and 2-fold faster for children less than 6 years than those above. Similarly, symptomatic children below 6 years had initial median CD4+ T-lymphocyte counts of 647 (22%) cells/muL, declining to 378 (20%) while those above 6 years had initial values of below 335 (15%) but which increased to 428 (17%). Median viral load correlated significantly with median CD4+ T-lymphocyte percentage in children above 6 years (p=0.026) but not below.

CONCLUSIONS

Viral load is lower in older than younger children and correlates significantly with percentage CD4+ T-lymphocytes. Survival by HIV-1 infected children requires a competent immune response early in infection to counter the rapidly replicating virus. Interventions aimed at boosting the naïve immune system may prolong survival in these children.

摘要

背景

在非洲,关于未接受治疗的HIV-1感染儿童中HIV-1 RNA载量、CD4+ T淋巴细胞及抗体反应与疾病进展关系的报道有限。

方法

为描述这些参数之间的关系,我们开展了一项纵向队列研究,纳入了51名1至13岁围产期感染HIV-1的儿童。通过ELISA确定HIV感染状态,并经western blot和PCR确认。通过有限稀释ELISA定量抗体,通过RT-PCR检测血浆HIV-1 RNA载量,通过FACSCount检测CD4+ T淋巴细胞。

结果

6岁以下儿童中,无症状和有症状疾病的HIV-1 RNA载量中位数分别从1195升至132543拷贝/毫升和从42962升至1109281拷贝/毫升。无症状儿童的病毒载量增加幅度比其他类别高10倍,6岁以下儿童的病毒载量增加速度比6岁以上儿童快2倍。同样,6岁以下有症状儿童的初始CD4+ T淋巴细胞计数中位数为647(22%)个/微升,降至378(20%),而6岁以上儿童的初始值低于335(15%),但升至428(17%)。6岁以上儿童的病毒载量中位数与CD4+ T淋巴细胞百分比中位数显著相关(p = 0.026),6岁以下儿童则不然。

结论

年龄较大儿童的病毒载量低于年龄较小儿童,且与CD4+ T淋巴细胞百分比显著相关。HIV-1感染儿童要存活,需要在感染早期有有效的免疫反应来对抗快速复制的病毒。旨在增强幼稚免疫系统的干预措施可能会延长这些儿童的生存期。

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