Barcelos Ivanildes Solange da Costa, Moura Leandro Pajuaba de, Costa Vinicius Paulino da, Ferreira Marcelo Simão, Costa-Cruz Julia Maria
Laboratório de Parasitologia, Instituto de Ciências Biomédicas, Universidade Federal de Uberlândia, Av. Pará 1720, 38400-902 Uberlândia, MG, Brasil.
Mem Inst Oswaldo Cruz. 2007 Sep;102(6):713-7. doi: 10.1590/s0074-02762007005000084.
The aim of this study was to test if serological distinction between patients with active and inactive neurocysticercosis (NCC), could be accomplished by the recognition of immunodominant peptides in total saline antigenic extract of Taenia solium metacestodes by IgG antibody in cerebrospinal fluid (CSF) and serum paired samples. CSF and serum samples of 10 each, active NCC patients, inactive NCC, and individuals with other neurological disorders, were used to recognize the antigenic peptides by western blot (WB). In the active NCC the 28-32 and 39-42 kDa peptides were more frequently detected in CSF than in sera (p < 0.05). The 47-52, 64-68, and 70 kDa antigens showed high frequencies in both samples from patients with active NCC. All the CSF samples of inactive NCC and other neurological disorder (control) patients tested negative, while serum samples from these last two groups recognized mainly the 80, 86, 95, and 98 kDa bands. This finding eliminates the use of the high molecular weigh bands (>or= 80 kDa) for diagnosis of NCC. The final conclusions were that the difference between active and inactive NCC may be done with the detection of peptides only in the CSF samples and that the 47-52, 64-68, and 70 kDa bands may be included as specific markers for active NCC when detected in CSF samples by WB using total saline extract of T. solium metacestode.
本研究的目的是检测通过脑脊液(CSF)和血清配对样本中的IgG抗体识别猪带绦虫幼虫全盐水抗原提取物中的免疫显性肽,是否能够实现活动性和非活动性神经囊尾蚴病(NCC)患者之间的血清学区分。分别采集10例活动性NCC患者、10例非活动性NCC患者以及10例患有其他神经系统疾病个体的CSF和血清样本,采用蛋白质印迹法(WB)识别抗原肽。在活动性NCC患者中,CSF中28 - 32 kDa和39 - 42 kDa的肽段比血清中更常被检测到(p < 0.05)。47 - 52 kDa、64 - 68 kDa和70 kDa的抗原在活动性NCC患者的两种样本中均有较高的检出率。所有非活动性NCC患者和其他神经系统疾病(对照)患者的CSF样本检测均为阴性,而这后两组患者的血清样本主要识别80、86、95和98 kDa的条带。这一发现排除了使用高分子量条带(≥80 kDa)诊断NCC的可能性。最终结论是,活动性和非活动性NCC之间的差异可能仅通过检测CSF样本中的肽段来实现,并且当使用猪带绦虫幼虫全盐水提取物通过WB在CSF样本中检测到47 - 52 kDa、64 - 68 kDa和70 kDa的条带时,可将其作为活动性NCC的特异性标志物。