Host-Parasite Interaction Group, Instituto de Investigação e Inovação em Saúde da Universidade do Porto, i3S, 4200-135 Oporto, Portugal.
Infectious Disease Department, Centro Hospitalar e Universitário de São João, Faculdade de Medicina da Universidade do Porto, 4200-319 Oporto, Portugal.
J Infect Public Health. 2024 May;17(5):810-818. doi: 10.1016/j.jiph.2024.03.008. Epub 2024 Mar 13.
In Europe, up to 70% of visceral leishmaniasis (VL) cases occurring in adults living with HIV. People living with HIV with VL co-infection often display persistent parasitemia, requiring chronic intermittent anti-Leishmania therapies. Consequently, frequent VL relapses and higher mortality rates are common in these individuals. As such, it is of paramount importance to understand the reasons for parasite persistence to improve infection management.
To outline possible causes for treatment failure in the context of HIV-VL, we followed a person living with HIV-VL co-infection for nine years in a 12-month period. We characterized: HIV-related clinicopathological alterations (CD4 T counts and viremia) and Leishmania-specific seroreactivity, parasitemia, quantification of pro-inflammatory cytokines upon stimulation and studied a Leishmania clinical isolate recovered during this period.
The subject presented controlled viremia and low CD4 counts. The subject remained PCR positive for Leishmania and also seropositive. The cellular response to parasite antigens was erratic. The isolate was identified as the first Leishmania infantum case with evidence of decreased miltefosine susceptibility in Portugal.
Treatment failure is a multifactorial process driven by host and parasite determinants. Still, the real-time determination of drug susceptibility profiles in clinical isolates is an unexplored resource in the monitoring of VL.
在欧洲,高达 70%的成人内脏利什曼病(VL)病例发生在 HIV 感染者中。HIV 合并 VL 感染的患者常表现出持续的寄生虫血症,需要进行慢性间歇性抗利什曼原虫治疗。因此,这些患者经常出现 VL 复发和更高的死亡率。因此,了解寄生虫持续存在的原因对于改善感染管理至关重要。
为了阐明 HIV-VL 背景下治疗失败的可能原因,我们在 12 个月的时间内对一名 HIV-VL 合并感染的患者进行了为期九年的随访。我们对 HIV 相关的临床病理改变(CD4 T 计数和病毒载量)和利什曼原虫特异性血清反应性、寄生虫血症、刺激后促炎细胞因子的定量以及在此期间恢复的利什曼临床分离株进行了特征描述。
患者的病毒载量得到了控制,CD4 计数较低。该患者仍对利什曼原虫 PCR 检测呈阳性,且血清学检测仍呈阳性。对寄生虫抗原的细胞反应不稳定。该分离株被鉴定为葡萄牙首例具有米替福新敏感性降低证据的利什曼原虫婴儿病例。
治疗失败是一个由宿主和寄生虫决定因素驱动的多因素过程。然而,在临床分离株中实时确定药物敏感性谱仍然是 VL 监测中尚未开发的资源。