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HIV感染儿童中HLA I类等位基因的母系与父系遗传:对临床疾病进展的影响

Maternal versus paternal inheritance of HLA class I alleles among HIV-infected children: consequences for clinical disease progression.

作者信息

Kuhn Louise, Abrams Elaine J, Palumbo Paul, Bulterys Marc, Aga Ronnie, Louie Leslie, Hodge Thomas

机构信息

Gertrude H. Sergievsky Center, College of Physicians and Surgeons, Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, New York 10032, USA.

出版信息

AIDS. 2004 Jun 18;18(9):1281-9. doi: 10.1097/00002030-200406180-00006.

Abstract

OBJECTIVE

When children acquire HIV infection from their mothers (with whom they share at least 50% of their HLA alleles), they acquire virus with a history of encounter with maternal HLA-mediated immune responses. We investigated whether maternal HLA selection pressures on the virus would adversely influence clinical outcomes of HIV-infected children.

METHODS

We tested whether time to AIDS diagnosis or death, among a cohort of 59 HIV-infected children in New York City followed from birth for up to 12 years, was associated with maternally- or paternally-inherited child HLA class I alleles, and with HLA similarity between mother and child.

RESULTS

HIV-infected children with an HLA allele usually associated with slow disease experienced a slower progression to AIDS or death only if the allele was paternally inherited. If the allele was present in the mother, no association was observed. Children who were homozygous or who shared both alleles with their mothers at more than one HLA class I locus were more likely to progress to AIDS or death than other children (relative hazard, 3.46; 95% confidence interval, 1.24-9.71).

CONCLUSION

Genetic similarity between mother and child may compromise the child's capacity to control HIV replication when the virus is acquired from the mother. HLA-mediated selective pressures on the virus in a transmitting mother-infant pair may undermine future HLA-mediated viral control in the child.

摘要

目的

当儿童从母亲那里感染艾滋病毒时(他们与母亲至少共享50%的人类白细胞抗原等位基因),他们所感染的病毒具有与母体人类白细胞抗原介导的免疫反应接触的历史。我们调查了母体对病毒的人类白细胞抗原选择压力是否会对感染艾滋病毒儿童的临床结局产生不利影响。

方法

我们测试了纽约市59名从出生起随访长达12年的感染艾滋病毒儿童中,艾滋病诊断或死亡时间是否与母系或父系遗传的儿童人类白细胞抗原I类等位基因以及母婴之间的人类白细胞抗原相似性有关。

结果

携带通常与疾病进展缓慢相关的人类白细胞抗原等位基因的感染艾滋病毒儿童,只有在该等位基因是父系遗传时,进展为艾滋病或死亡的速度才较慢。如果该等位基因存在于母亲体内,则未观察到相关性。在一个以上人类白细胞抗原I类位点上纯合或与母亲共享两个等位基因的儿童比其他儿童更有可能进展为艾滋病或死亡(相对风险,3.46;95%置信区间,1.24 - 9.71)。

结论

当病毒从母亲那里获得时,母婴之间的基因相似性可能会损害儿童控制艾滋病毒复制的能力。在母婴传播对中,母体对病毒的人类白细胞抗原介导的选择压力可能会破坏儿童未来人类白细胞抗原介导的病毒控制。

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