首页> 外文期刊>Transactions of the Royal Society of Tropical Medicine and Hygiene >Isolation and molecular characterization of recombinant Echinococcus granulosus P29 protein (recP29) and its assessment for the post-surgical serological follow-up of human cystic echinococcosis in young patients.
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Isolation and molecular characterization of recombinant Echinococcus granulosus P29 protein (recP29) and its assessment for the post-surgical serological follow-up of human cystic echinococcosis in young patients.

机译:重组细粒棘球E虫P29蛋白(recP29)的分离和分子特征及其对年轻患者人囊性棘球co虫病的术后血清学随访的评估。

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摘要

We synthesized recombinant Echinococcus granulosus protoscolex recP29 antigen to be preliminarily assessed by ELISA and immunoblotting. RecP29-serology was carried out on 54 young patients with cystic echinococcosis (CE). Patients were classified into either cured (CCE) (n=40) or non-cured (NCCE) (n=14) CE patients. RecP29 ELISA showed a gradual decrease of antibody concentrations in all CCE cases that were initially (before treatment) seropositive to this antigen (25 out of 40) or that seroconverted following treatment. A complete seronegativity was reached within 3 years post-surgery in all of these cases. Conventional HCF ELISA yielded seronegativity in only 10% of initially recP29-seropositive CCE patients (P=0.086). Likewise, recP29 immunoblotting yielded seronegativity in 93% of 29 out of 40 initially recP29-immunoblot-positive CCE patients after 3 years follow-up, compared with 72% in the HCF immunoblotting (P=0.060). Eleven out of 14 NCCE patients were initially positive by recP29 ELISA, and 10out of these maintained a marked anti-recP29 antibody reactivity until the endpoint of the follow-up period. All 14 NCCE cases were initially seropositive by recP29 immunoblotting, and 13 cases remained seropositive until the end of the study. Thus, recombinant P29 protein appears prognostically useful for monitoring those post-surgical CE cases with an initial seropositivity to this marker.
机译:我们合成了重组细粒棘球proprotoscolex recP29抗原,将通过ELISA和免疫印迹进行初步评估。对54例年轻的囊性棘球young病(CE)患者进行了RecP29血清学检查。患者分为治愈(CCE)(n = 40)或未治愈(NCCE)(n = 14)CE患者。 RecP29 ELISA显示,在最初(治疗前)对该抗原呈血清反应阳性的所有CCE病例(40个病例中有25个)或在治疗后发生血清转化的所有CCE病例中,抗体浓度逐渐降低。在所有这些情况下,术后3年内即可达到完全的血清阴性反应。常规HCF ELISA仅在最初recP29血清阳性的CCE患者中有10%产生血清阴性反应(P = 0.086)。同样,recP29免疫印迹在随访3年后,在40例最初的recP29免疫印迹阳性CCE患者中,有29%的93%产生了血清阴性反应,而HCF免疫印迹则为72%(P = 0.060)。 14名NCCE患者中有11名最初通过recP29 ELISA呈阳性,其中10名维持了显着的抗recP29抗体反应性,直至随访期结束。通过recP29免疫印迹分析,所有14例NCCE最初都呈血清阳性,直到研究结束之前,还有13例呈阳性。因此,重组P29蛋白在预后上可用于监测那些对该标志物具有初始血清阳性的手术后CE病例。

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