Muhimbili Medical Research Center, National Institute for Medical Research (NIMR), Dar es Salaam, Tanzania.
Institute for Medical Microbiology, Immunology, and Hygiene, Technical University of Munich (TUM), Munich, Germany.
PLoS Negl Trop Dis. 2024 Aug 2;18(8):e0012345. doi: 10.1371/journal.pntd.0012345. eCollection 2024 Aug.
The parasitic infection caused by Taenia solium represents a significant public health concern in developing countries. Larval invasion of body tissues leads to cysticercosis (CC), while central nervous system (CNS) involvement results in neurocysticercosis (NCC). Both conditions exhibit diverse clinical manifestations, and the potential impact of concomitant HIV infection especially prevalent in sub-Saharan Africa on peripheral and CNS immune responses remains poorly understood. This study aimed to identify the potential impact of HIV coinfection in CC and NCC patients.
A nested study within a cross-sectional analysis in two Tanzanian regions was performed and 234 participants (110 HIV+ and 124 HIV-) were tested for cysticercosis antibodies, antigens, CD4 counts and serum Th1 and Th2 cytokines via multiplex bead-based immunoassay. 127 cysticercosis seropositive individuals underwent cranial computed tomography (CCT) and clinical symptoms were assessed. Multiple regression analyses were performed to identify factors associated with cytokine modulation due to HIV in CC and NCC patients.
Serologically, 18.8% tested positive for cysticercosis antibodies, with no significant difference HIV+ and HIV+. A significantly higher rate of cysticercosis antigen positivity was found in HIV+ individuals (43.6%) compared to HIV- (28.2%) (p = 0.016). CCT scans revealed that overall 10.3% had active brain cysts (NCC+). Our study found no significant changes in the overall cytokine profiles between HIV+ and HIV- participants coinfected CC and NCC, except for IL-5 which was elevated in HIV+ individuals with cysticercosis. Furthermore, HIV infection in general was associated with increased levels of pro-and some anti-inflammatory cytokines e.g. TNF-α, IL-8, and IFN-γ. However, based on the interaction analyses, no cytokine changes were observed due to HIV in CC or NCC patients.
In conclusion, while HIV infection itself significantly modulates levels of key cytokines such as TNF-α, IL-8, and IFN-γ, it does not modulate any cytokine changes due to CC or NCC. This underscores the dominant influence of HIV on the immune system and highlights the importance of effective antiretroviral therapy in managing immune responses in individuals coinfected with HIV and CC/NCC.
猪带绦虫引起的寄生虫感染是发展中国家的一个重大公共卫生问题。幼虫侵入身体组织导致囊虫病(CC),而中枢神经系统(CNS)受累则导致神经囊虫病(NCC)。这两种情况都表现出不同的临床表现,而 HIV 感染的潜在影响,特别是在撒哈拉以南非洲地区,对周围和中枢免疫反应的潜在影响仍知之甚少。本研究旨在确定 HIV 合并感染对 CC 和 NCC 患者的潜在影响。
在坦桑尼亚两个地区进行的横断面分析中的嵌套研究中,对 234 名参与者(110 名 HIV+和 124 名 HIV-)进行了囊虫病抗体、抗原、CD4 计数以及血清 Th1 和 Th2 细胞因子的检测,采用基于多重珠的免疫分析。对 127 名囊虫病血清阳性个体进行了头颅计算机断层扫描(CCT),并评估了临床症状。采用多元回归分析确定与 HIV 相关的细胞因子调节因素,这些因素与 CC 和 NCC 患者有关。
血清学检测显示,18.8%的人对囊虫病抗体呈阳性,HIV+和 HIV-之间无显著差异。HIV+个体的囊虫病抗原阳性率(43.6%)明显高于 HIV-个体(28.2%)(p=0.016)。CCT 扫描显示,总体上有 10.3%的人有活动性脑囊虫(NCC+)。我们的研究发现,在合并感染 CC 和 NCC 的 HIV+和 HIV-参与者中,细胞因子谱总体上没有显著变化,除了 HIV+的囊虫病患者中 IL-5 升高。此外,HIV 感染通常与促炎和一些抗炎细胞因子如 TNF-α、IL-8 和 IFN-γ水平升高有关。然而,基于交互分析,在 CC 或 NCC 患者中,未观察到由于 HIV 引起的细胞因子变化。
综上所述,尽管 HIV 感染本身显著调节 TNF-α、IL-8 和 IFN-γ等关键细胞因子的水平,但它不会调节 CC 或 NCC 引起的任何细胞因子变化。这突出了 HIV 对免疫系统的主要影响,并强调了在 HIV 合并 CC/NCC 感染个体中,有效抗逆转录病毒治疗对管理免疫反应的重要性。