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Transmission of HIV-1 Gag immune escape mutations is associated with reduced viral load in linked recipients.HIV-1衣壳蛋白免疫逃逸突变的传播与相关接受者体内病毒载量降低有关。
J Exp Med. 2008 May 12;205(5):1009-17. doi: 10.1084/jem.20072457. Epub 2008 Apr 21.
2
Transmission of HIV-1 CTL escape variants provides HLA-mismatched recipients with a survival advantage.HIV-1细胞毒性T淋巴细胞逃逸变体的传播为HLA不匹配的受体提供了生存优势。
PLoS Pathog. 2008 Mar 21;4(3):e1000033. doi: 10.1371/journal.ppat.1000033.
3
The relation between symptoms, viral load, and viral load set point in primary HIV infection.原发性HIV感染中症状、病毒载量及病毒载量设定点之间的关系。
J Acquir Immune Defic Syndr. 2007 Aug 1;45(4):445-8. doi: 10.1097/QAI.0b013e318074ef6e.
4
Higher set point plasma viral load and more-severe acute HIV type 1 (HIV-1) illness predict mortality among high-risk HIV-1-infected African women.较高的设定点血浆病毒载量和更严重的1型急性艾滋病毒(HIV-1)疾病预示着高危感染HIV-1的非洲女性的死亡率。
Clin Infect Dis. 2006 May 1;42(9):1333-9. doi: 10.1086/503258. Epub 2006 Mar 27.
5
Fitness cost of escape mutations in p24 Gag in association with control of human immunodeficiency virus type 1.与1型人类免疫缺陷病毒控制相关的p24 Gag逃逸突变的适应性代价
J Virol. 2006 Apr;80(7):3617-23. doi: 10.1128/JVI.80.7.3617-3623.2006.
6
HLA allele sharing and HIV type 1 viremia in seroconverting Zambians with known transmitting partners.已知传播伴侣的血清转化期赞比亚人中的HLA等位基因共享与1型艾滋病毒血症
AIDS Res Hum Retroviruses. 2004 Jan;20(1):19-25. doi: 10.1089/088922204322749468.
7
Reversion of CTL escape-variant immunodeficiency viruses in vivo.体内细胞毒性T淋巴细胞逃逸变异免疫缺陷病毒的逆转
Nat Med. 2004 Mar;10(3):275-81. doi: 10.1038/nm998. Epub 2004 Feb 15.
8
Relationship between in vitro human immunodeficiency virus type 1 replication rate and virus load in plasma.体外1型人类免疫缺陷病毒复制率与血浆病毒载量之间的关系。
J Virol. 2003 Nov;77(22):12105-12. doi: 10.1128/jvi.77.22.12105-12112.2003.
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Virus load during primary Human Immunodeficiency Virus (HIV) type 1 infection is related to the severity of acute HIV illness in Kenyan women.在肯尼亚女性中,1型人类免疫缺陷病毒(HIV)初次感染期间的病毒载量与急性HIV疾病的严重程度相关。
Clin Infect Dis. 2002 Jul 1;35(1):77-81. doi: 10.1086/340862. Epub 2002 Jun 3.
10
Use of laboratory tests and clinical symptoms for identification of primary HIV infection.利用实验室检测和临床症状来识别原发性HIV感染。
AIDS. 2002 May 24;16(8):1119-29. doi: 10.1097/00002030-200205240-00005.

HIV RNA 水平在早期感染中可由传播源中的病毒载量预测。

HIV RNA level in early infection is predicted by viral load in the transmission source.

机构信息

HIV/AIDS Division, Department of Medicine, San Francisco General Hospital, University of California, CA 94110, USA.

出版信息

AIDS. 2010 Apr 24;24(7):941-5. doi: 10.1097/QAD.0b013e328337b12e.

DOI:10.1097/QAD.0b013e328337b12e
PMID:20168202
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2887742/
Abstract

OBJECTIVE

HIV-1 viral load in early infection predicts the risk of subsequent disease progression but the factors responsible for the differences between individuals in viral load during this period have not been fully identified. We sought to determine the relationship between HIV-1 RNA levels in the source partner and recently infected recipient partners within transmission pairs.

METHODS

We recruited donor partners of persons who presented with acute or recent (<6 months) HIV infection. Transmission was confirmed by phylogenetic comparison of virus sequence in the donor and recipient partners. We compared viral load in the donor partner and the recipient in the first 6 months of HIV infection.

RESULTS

We identified 24 transmission pairs. The median estimated time from infection to evaluation in acutely/recently infected recipient individuals was 72 days. The viral load in the donor was closely associated with viral load at presentation in the recipient case (r = 0.55, P = 0.006).

CONCLUSION

The strong correlation between HIV-1 RNA levels within HIV transmission pairs indicates that virus characteristics are an important determinant of viral load in early HIV infection.

摘要

目的

HIV-1 病毒载量在早期感染中可预测随后疾病进展的风险,但导致个体在该时期病毒载量差异的因素尚未完全确定。我们旨在确定传播对中 HIV-1 病毒载量处于早期感染的源伴侣和新感染的受体伴侣之间的关系。

方法

我们招募了具有急性或近期(<6 个月)HIV 感染的个体的供体伴侣。通过对供体和受体伴侣病毒序列的系统发生比较来确认传播。我们比较了 HIV 感染的前 6 个月中供体伴侣和受体的病毒载量。

结果

我们确定了 24 个传播对。在急性/近期感染的受体个体中,从感染到评估的中位估计时间为 72 天。供体中的病毒载量与受体病例中的初始病毒载量密切相关(r = 0.55,P = 0.006)。

结论

HIV 传播对中 HIV-1 RNA 水平之间的强相关性表明,病毒特征是 HIV 早期感染中病毒载量的重要决定因素。