免疫重建炎症综合征在开始抗逆转录病毒治疗后表现为牛皮癣:一个病例报告。

M. Cheaito, M. Khalifeh, Batoul Jaafar, Nesrine A. Rizk
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摘要

随着抗逆转录病毒联合治疗(cART)的使用,艾滋病毒和艾滋病的负担已经减轻。免疫重建炎症综合征(IRIS)是cART启动或再次引入时出现的并发症。尽管已有多种IRIS定义,但对于临床上有用的定义仍未达成共识。基于病理生理学,IRIS在临床上可分为两类:它是由先前的亚临床感染引起的,该感染在开始抗逆转录病毒治疗后被免疫反应揭开(揭开IRIS),或者是由最近治疗的机会性感染的矛盾复发引起的(矛盾IRIS)。银屑病见于晚期艾滋病毒和免疫抑制,其症状通常在开始cART和免疫恢复后消退。有三种理论被提出来解释HIV中的牛皮癣:CD8+ T细胞与CD4+ T细胞比例的不平衡,调节性T细胞(Treg)的不平衡,以及HIV作为CD8+ T细胞的共刺激因子。然而,在这个病例报告中,我们描述了IRIS作为牛皮癣的矛盾表现,在重新启动cART后看到。据我们所知,这是文献中报告的第二例病例。我们正在描述一个39岁的黎巴嫩男子的病例,他长期感染艾滋病毒,在过去的八年中,他的cART依从性很差。患者有三次牛皮癣发作,与cART的重新开始一致。我们建议,该患者不遵守cART,导致CD4/CD8比值低且无法恢复,导致IRIS表现为牛皮癣。此外,Treg的功能障碍可能是IRIS牛皮癣的另一个可能的解释,类似于HIV相关牛皮癣的功能障碍。因此,我们认为IRIS可以表现为牛皮癣;然而,为了更清楚地了解这些复杂的免疫现象,还需要进行更多的研究。
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Immune Reconstitution Inflammatory Syndrome Presenting as Psoriasis After Initiating Antiretroviral Therapy: A Case-Report.
The burden of HIV and AIDS has been reduced with the utilization of combination antiretroviral therapy (cART). Immune reconstitution inflammatory syndrome (IRIS) is a complication seen with either the initiation or the reintroduction of cART. Although multiple IRIS definitions have been used, there is still no consensus on a clinically useful definition. Based on the pathophysiology, IRIS can be clinically grouped into two categories: it is either caused by a previously subclinical infection that was unmasked by the immune response following the initiation of ART (unmasking IRIS) or by the paradoxical relapse of a recently treated opportunistic infection (paradoxical IRIS). Psoriasis is seen with advanced HIV and immunosuppression and its symptoms typically recede after the initiation of cART and immune restoration. Three theories have been proposed to explain psoriasis in HIV: an imbalance in the CD8+ T-cells to CD4+ T-cells ratio, an imbalance of regulatory T cells (Treg), and HIV acting as a co-stimulatory factor to CD8+ T-cells. However, in this case report, we are describing the paradoxical presentation of IRIS as psoriasis, seen after reinitiating of cART. To our knowledge, this is the second reported case in the literature. We are describing a case of a 39-year-old Lebanese man with long-standing HIV infection and poor cART compliance over the past eight years. The patient has had three flares of psoriasis that coincided with the re-initiation of cART. We are proposing that this patient’s noncompliance with cART and the resulting low, non-recovering CD4/CD8 ratio lead to IRIS presenting as psoriasis. Additionally, a dysfunction in Treg may be another probable explanation for IRIS psoriasis similar to the dysfunction seen with HIV associated psoriasis. Therefore, we conclude that IRIS can present as psoriasis; however, more research is needed in order to make the picture of these complex immune phenomena clearer.
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