Previato Mariana, Frederico Fábio Batista, Murata Fernando Henrique Antunes, Siqueira Rubens Camargo, Barbosa Amanda Pires, Silveira-Carvalho Aparecida Perpétuo, Meira Cristina da Silva, Pereira-Chioccola Vera Lúcia, Gava Ricardo, Martins Neto Plínio Pereira, de Mattos Luiz Carlos, de Mattos Cinara Cássia Brandão
Immunogenetics Laboratory, Department of Molecular Biology, Faculdade de Medicina de São José do Rio Preto-FAMERP, Avenida Brigadeiro Faria Lima, 5416, São José do Rio Preto, Sao Paulo state, 15090-000, Brazil.
FAMERP Toxoplasma Research Group, Avenida Brigadeiro Faria Lima, 5416, São José do Rio Preto, Sao Paulo state, 15090-000, Brazil.
BMC Res Notes. 2015 Dec 7;8:746. doi: 10.1186/s13104-015-1650-6.
Toxoplasmosis was recently included as a neglected disease by the Center for Disease Control. Ocular toxoplasmosis is one clinical presentation of congenital or acquired infection. The laboratory diagnosis is being used worldwide to support the clinical diagnosis and imaging. The aim of this study was to evaluate the use of serology and molecular methods to monitor acute OT in immunocompetent patients during treatment.
Five immunocompetent patients were clinically diagnosed with acute OT. The clinical evaluation was performed by ophthalmologic examination using the Early Treatment Diabetic Retinopathy Study, best-corrected visual acuity, slit lamp biomicroscopy, fundoscopic examination with indirect binocular ophthalmoscopy color fundus photography, fluorescein angiography and spectral optical coherence tomography (OCT). Serology were performed by ELISA (IgA, IgM, IgG) and confirmed by ELFA (IgG, IgM). Molecular diagnoses were performed in peripheral blood by cPCR using the Toxoplasma gondii B1 gene as the marker. Follow-up exams were performed on day +15 and day +45.
Only five non-immunocompromised male patients completed the follow up and their data were used for analysis. The mean age was 41.2 ± 11.3 years (median: 35; range 31-54 years). All of them were positive for IgG antibodies but with different profiles for IgM and IgA, as well as PCR. For all patients the OCT exam showed active lesions with the inner retinal layers being abnormally hyper-reflective with full-thickness disorganization of the retinal reflective layers, which assumed a blurred reflective appearance and the retina was thickened.
The presence of IgA and IgM confirmed the acute infection and thus was in agreement with the clinical evaluation. Our results show the adopted treatment modified the serological profile of IgM antibodies and the PCR results, but not the IgG and IgA antibodies and that imaging is a good tool to follow-up patients.
弓形虫病最近被疾病控制中心列为一种被忽视的疾病。眼部弓形虫病是先天性或获得性感染的一种临床表现。实验室诊断在全球范围内被用于辅助临床诊断和影像学检查。本研究的目的是评估血清学和分子方法在免疫功能正常的患者治疗期间监测急性眼部弓形虫病的应用。
5名免疫功能正常的患者被临床诊断为急性眼部弓形虫病。通过眼科检查进行临床评估,采用糖尿病视网膜病变早期治疗研究、最佳矫正视力、裂隙灯生物显微镜检查、间接双目检眼镜彩色眼底摄影的眼底镜检查、荧光素血管造影和光谱光学相干断层扫描(OCT)。血清学检测采用ELISA法(检测IgA、IgM、IgG),并通过ELFA法(检测IgG、IgM)进行确认。分子诊断通过使用弓形虫B1基因作为标志物的cPCR在外周血中进行。在第15天和第45天进行随访检查。
只有5名非免疫功能低下的男性患者完成了随访,他们的数据用于分析。平均年龄为41.2±11.3岁(中位数:35岁;范围31 - 54岁)。他们所有的IgG抗体均为阳性,但IgM和IgA以及PCR的结果各不相同。对于所有患者,OCT检查显示有活动性病变,视网膜内层异常高反射,视网膜反射层全层紊乱,呈现模糊的反射外观,视网膜增厚。
IgA和IgM的存在证实了急性感染,因此与临床评估结果一致。我们的结果表明,所采用的治疗改变了IgM抗体的血清学特征和PCR结果,但未改变IgG和IgA抗体,并且影像学检查是随访患者的良好工具。