da Cruz Allecineia Bispo, Carneiro Francieli Marinho, Taniwaki Noemi Nosomi, Namiyama Gislene Mitsue, Dos Santos Débora Oliveira, Castellão Katia Gomes, Ferreira Isabelle Martins Ribeiro, Hiramoto Roberto Mitsuyoshi, Pereira-Chioccola Vera Lucia
Parasitology and Mycology Center, Adolfo Lutz Institute, Sao Paulo, Brazil.
Graduate Program in Science, Coordinator for Disease Control, Ministry of Health of São Paulo State, Sao Paulo, Brazil.
J Parasitol Res. 2025 Jan 21;2025:8355886. doi: 10.1155/japr/8355886. eCollection 2025.
Visceral leishmaniasis (VL) is a zoonotic disease in which dogs are the main reservoirs. Until now, the serological tests do not present satisfactory sensitivity for diagnosis of these hosts. One of the functions of extracellular vesicles (EVs) is related to immunological host response. Here, we evaluated the ability of EVs released by promastigotes (Leish-EVs) to be source of antigens for use in serological diagnosis for human visceral leishmaniasis (HumVL) and canine visceral leishmaniasis (CanVL). A total of 300 sera were tested. The 155 human sera were divided into 4 groups and 145 canine sera into 3 groups. In human sera, Leish-EVs were reactive in 73/74 sera from patients with VL (Hum-VL) with 98.64% sensitivity. The 26 sera from healthy individuals (NH) and 27 from individuals with asymptomatic toxoplasmosis (ATx) were nonreagent (100% specificity). Leish-EVs-ELISA had cross-reactivity or inconclusive results in 13.5% of sera from Chagas disease patients (CD). In canine sera, Leish-EVs were reactive in 60/63 sera from dogs with CanVL (Can-VL) with 95.24% sensitivity. Leish-EVs were nonreactive in sera from 57 dogs without Can-VL (NC) and 25 with other infections (OIs) with 100% specificity. Hum-VL produced more IgG1 against Leish-EVs than IgG2, IgG3, and IgG4. Can-VL produced more IgG2 against Leish-EVs than IgG1. In conclusion, this study provides evidence that Leish-EVs released by when used as antigen in ELISA identified the host antibodies. The methodology was effective for serological diagnosis of VL, since results exhibited good sensitivity and specificity for human and canine sera.
内脏利什曼病(VL)是一种人畜共患病,狗是主要储存宿主。到目前为止,血清学检测对这些宿主的诊断敏感性并不令人满意。细胞外囊泡(EVs)的功能之一与宿主免疫反应有关。在此,我们评估了前鞭毛体释放的细胞外囊泡(Leish-EVs)作为抗原用于人类内脏利什曼病(HumVL)和犬内脏利什曼病(CanVL)血清学诊断的能力。共检测了300份血清。155份人类血清分为4组,145份犬血清分为3组。在人类血清中,Leish-EVs在74份VL患者(Hum-VL)血清中的73份中有反应,敏感性为98.64%。26份健康个体(NH)血清和27份无症状弓形虫病(ATx)个体血清无反应(特异性为100%)。Leish-EVs-ELISA在13.5%的恰加斯病患者(CD)血清中有交叉反应或不确定结果。在犬血清中,Leish-EVs在63份CanVL犬(Can-VL)血清中的60份中有反应,敏感性为95.24%。Leish-EVs在57份无Can-VL(NC)的犬血清和25份有其他感染(OIs)的犬血清中无反应,特异性为100%。Hum-VL产生的针对Leish-EVs的IgG1比IgG2、IgG3和IgG4更多。Can-VL产生的针对Leish-EVs的IgG2比IgG1更多。总之,本研究提供了证据表明,前鞭毛体释放的Leish-EVs在ELISA中用作抗原时可识别宿主抗体。该方法对VL血清学诊断有效,因为结果对人类和犬血清均显示出良好的敏感性和特异性。