Ribeiro Bruno de Paulo, Cassiano Gustavo Capatti, de Souza Rodrigo Medeiros, Cysne Dalila Nunes, Grisotto Marcos Augusto Grigolin, de Azevedo dos Santos Ana Paula Silva, Marinho Cláudio Romero Farias, Machado Ricardo Luiz Dantas, Nascimento Flávia Raquel Fernandes
Programa de Pós- graduação em Ciências da Saúde, Universidade Federal do Maranhão (UFMA), São Luís, Maranhão, Brazil.
Laboratório de Imunofisiologia, Universidade Federal do Maranhão (UFMA), São Luís, Maranhão, Brazil.
PLoS Negl Trop Dis. 2016 Mar 4;10(3):e0004479. doi: 10.1371/journal.pntd.0004479. eCollection 2016 Mar.
Mechanisms involved in severe P. vivax malaria remain unclear. Parasite polymorphisms, parasite load and host cytokine profile may influence the course of infection. In this study, we investigated the influence of circumsporozoite protein (CSP) polymorphisms on parasite load and cytokine profile in patients with vivax malaria. A cross-sectional study was carried out in three cities: São Luís, Cedral and Buriticupu, Maranhão state, Brazil, areas of high prevalence of P. vivax. Interleukin (IL)-2, IL-4, IL-10, IL-6, IL-17, tumor necrosis factor alpha (TNF-α, interferon gamma (IFN-γ and transforming growth factor beta (TGF-β were quantified in blood plasma of patients and in supernatants from peripheral blood mononuclear cell (PBMC) cultures. Furthermore, the levels of cytokines and parasite load were correlated with VK210, VK247 and P. vivax-like CSP variants. Patients infected with P. vivax showed increased IL-10 and IL-6 levels, which correlated with the parasite load, however, in multiple comparisons, only IL-10 kept this association. A regulatory cytokine profile prevailed in plasma, while an inflammatory profile prevailed in PBMC culture supernatants and these patterns were related to CSP polymorphisms. VK247 infected patients showed higher parasitaemia and IL-6 concentrations, which were not associated to IL-10 anti-inflammatory effect. By contrast, in VK210 patients, these two cytokines showed a strong positive correlation and the parasite load was lower. Patients with the VK210 variant showed a regulatory cytokine profile in plasma, while those infected with the VK247 variant have a predominantly inflammatory cytokine profile and higher parasite loads, which altogether may result in more complications in infection. In conclusion, we propose that CSP polymorphisms is associated to the increase of non-regulated inflammatory immune responses, which in turn may be associated with the outcome of infection.
间日疟原虫重症疟疾所涉及的机制仍不清楚。寄生虫多态性、寄生虫载量和宿主细胞因子谱可能会影响感染进程。在本研究中,我们调查了环子孢子蛋白(CSP)多态性对间日疟患者寄生虫载量和细胞因子谱的影响。在巴西马兰热州的三个城市——圣路易斯、塞德拉尔和布里蒂库普进行了一项横断面研究,这些地区是间日疟原虫的高流行区。对患者血浆以及外周血单核细胞(PBMC)培养上清液中的白细胞介素(IL)-2、IL-4、IL-10、IL-6、IL-17、肿瘤坏死因子α(TNF-α)、干扰素γ(IFN-γ)和转化生长因子β(TGF-β)进行了定量分析。此外,细胞因子水平和寄生虫载量与VK210、VK247和间日疟原虫样CSP变体相关。感染间日疟原虫的患者IL-10和IL-6水平升高,这与寄生虫载量相关,然而,在多重比较中,只有IL-10保持这种关联。血浆中以调节性细胞因子谱为主,而PBMC培养上清液中以炎症性细胞因子谱为主,这些模式与CSP多态性有关。感染VK247的患者表现出更高的寄生虫血症和IL-6浓度,这与IL-10的抗炎作用无关。相比之下,在感染VK210的患者中,这两种细胞因子呈强正相关,且寄生虫载量较低。携带VK210变体的患者血浆中呈现调节性细胞因子谱,而感染VK247变体的患者主要呈现炎症性细胞因子谱且寄生虫载量更高,这可能共同导致感染中出现更多并发症。总之,我们认为CSP多态性与非调节性炎症免疫反应的增加有关,这反过来可能与感染结果相关。