Das Sanchita, Mahajan R C, Ganguly N K, Sawhney I M S, Dhawan Veena, Malla Nancy
Department of Parasitology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Trop Med Int Health. 2002 Jan;7(1):53-8. doi: 10.1046/j.1365-3156.2002.00810.x.
Neurocysticercosis (NCC) is a major cause of morbidity and mortality in developed and developing countries. The diagnosis of this disease remains a problem. We report the detection of specific antigenic fraction (antigen B) of Cysticercus cellulosae by enzyme-linked immunosorbent assay (ELISA) in various fractions of cerebrospinal fluid (CSF) obtained by high performance liquid chromatographic (HPLC) separation, for the diagnosis of human NCC. Forty patients attending or admitted to Nehru Hospital, Chandigarh were included in the study: 10 with suspected NCC, 20 with other neurological diseases and 10 undergoing surgery under spinal anaesthesia for non-neurological conditions, who served as controls. CSF samples collected from all patients and controls were subjected to chromatographic separation on an HPLC system. Antigen B (AgB) was detected in separated fractions by an ELISA test and compared with the detection of antibody response in CSF samples by indirect haemagglutination (IHA) technique. Antigen B was detected in 9 out of 10 patients with suspected NCC based on clinical symptoms and radioimaging reports, but in none of the control subjects. However, antigen B was also detected in 9 out of 20 patients with other neurological disorders, mostly tubercular meningitis. Antibody response by IHA was found positive in only 2 of 10 cases clinically suspected of NCC. In conclusion, antigen B detection in CSF samples may be a useful adjunct to clinical suspicion and radiological reports for the diagnosis of NCC as there is no gold standard criteria to confirm this disease. However, the test needs to be evaluated on more patients in countries where tuberculosis and cysticercosis are endemic due to the high cross reactivity with samples from tubercular meningitis patients.
神经囊尾蚴病(NCC)是发达国家和发展中国家发病和死亡的主要原因。该疾病的诊断仍然是一个难题。我们报告了通过高效液相色谱(HPLC)分离获得的脑脊液(CSF)不同组分中,采用酶联免疫吸附测定(ELISA)检测猪囊尾蚴的特异性抗原组分(抗原B),用于诊断人类NCC。纳入研究的40例患者来自昌迪加尔的尼赫鲁医院,其中10例疑似NCC,20例患有其他神经系统疾病,10例因非神经系统疾病在脊髓麻醉下接受手术,作为对照。收集所有患者和对照的CSF样本,在HPLC系统上进行色谱分离。通过ELISA试验在分离的组分中检测抗原B(AgB),并与通过间接血凝(IHA)技术检测CSF样本中的抗体反应进行比较。基于临床症状和影像学报告,10例疑似NCC患者中有9例检测到抗原B,但对照受试者均未检测到。然而,20例患有其他神经系统疾病的患者中,有9例也检测到抗原B,大多数为结核性脑膜炎。临床疑似NCC的10例患者中,仅2例IHA抗体反应呈阳性。总之,由于没有确诊该疾病的金标准,CSF样本中抗原B的检测可能是临床怀疑和影像学报告诊断NCC的有用辅助手段。然而,由于与结核性脑膜炎患者样本的交叉反应性高,在结核病和囊尾蚴病流行的国家,需要对更多患者进行该检测评估。