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HIV易感性和保护性HLA等位基因的共同出现可能是原发性HIV相关血小板减少症(PHAT)发生的一个因素:一项横断面研究。

Co-Occurrence of HIV-Susceptibility and -Protective HLA Alleles Is a Possible Contributor to the Development of Primary HIV-Associated Thrombocytopenia (PHAT): A Cross-Sectional Study.

作者信息

van Rensburg Walter J Janse, Marle Anne-Cecilia van, Geertsema Lomari

机构信息

Human Molecular Biology Unit, School of Biomedical Sciences, Faculty of Health Sciences, University of the Free State, Bloemfontein, South Africa.

Department of Haematology and Cell Biology, School of Pathology, Faculty of Health Sciences, University of the Free State, Bloemfontein, South Africa.

出版信息

Int J Immunogenet. 2025 Oct;52(5):249-255. doi: 10.1111/iji.70003. Epub 2025 Jul 14.

Abstract

Primary HIV-associated thrombocytopenia (PHAT) is an isolated thrombocytopenia in HIV-positive individuals in the absence of secondary causes. The presence of certain Human Leukocyte Antigens (HLA) has been linked to individuals' immune response to HIV and the development of immune-mediated thrombocytopenic disorders. Considering the established associations between HLA and HIV infection and HLA and immune-mediated thrombocytopenias, we hypothesise that specific HLA alleles may also increase the risk of developing PHAT, a condition that links both HIV and immune-mediated thrombocytopenia. Therefore, the study aimed to determine the frequency of high-resolution HLA alleles in patients presenting with possible PHAT. Following a detailed screening process, we evaluated the HLA profiles of 43 participants with probable PHAT using the Axiom Precision Medicine Diversity Array (PMDA) Kit on the GeneTitan Multi-Channel instrument. No single HLA allele was found to be more prominent in our PHAT population. However, 93.02% of participants had both HIV-protective and HIV-susceptible alleles. The potential mechanism causing thrombocytopenia to be the only clinically relevant haematological abnormality in these patients remains to be explored. We concluded that the presence of both an HIV-protective and HIV-susceptibility allele in the same individual may cause antagonistic immune reactions, resulting in thrombocytopenia in HIV-positive individuals. We propose future long-term follow-up studies to determine the progression and outcome in patients with PHAT.

摘要

原发性HIV相关血小板减少症(PHAT)是指HIV阳性个体在无继发原因情况下出现的孤立性血小板减少症。某些人类白细胞抗原(HLA)的存在与个体对HIV的免疫反应以及免疫介导的血小板减少性疾病的发生有关。鉴于HLA与HIV感染之间以及HLA与免疫介导的血小板减少症之间已确立的关联,我们推测特定的HLA等位基因可能也会增加患PHAT的风险,PHAT是一种将HIV与免疫介导的血小板减少症联系起来的病症。因此,本研究旨在确定可能患有PHAT的患者中高分辨率HLA等位基因的频率。经过详细的筛查过程,我们使用基因分型仪上的Axiom精准医学多样性阵列(PMDA)试剂盒评估了43名可能患有PHAT的参与者的HLA谱。在我们的PHAT人群中未发现单一的HLA等位基因更为突出。然而,93.02%的参与者同时具有HIV保护性和HIV易感性等位基因。导致血小板减少成为这些患者唯一临床相关血液学异常的潜在机制仍有待探索。我们得出结论,同一个体中同时存在HIV保护性和HIV易感性等位基因可能会引发拮抗免疫反应,导致HIV阳性个体出现血小板减少症。我们建议未来进行长期随访研究,以确定PHAT患者的病情进展和预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8ce/12418909/cac127bec079/IJI-52-249-g001.jpg

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