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美国用于检测免疫球蛋白IgG和IgM的三种即时检验方法的评估:概念验证与挑战

Evaluation of Three Point-of-Care Tests for Detection of Immunoglobulin IgG and IgM in the United States: Proof of Concept and Challenges.

作者信息

Gomez Carlos A, Budvytyte Laura N, Press Cindy, Zhou Lily, McLeod Rima, Maldonado Yvonne, Montoya Jose G, Contopoulos-Ioannidis Despina G

机构信息

Division of Infectious Diseases and Geographic Medicine, Department of Medicine, Stanford University School of Medicine, California.

Palo Alto Medical Foundation Toxoplasma Serology Laboratory, National Reference Center for the Study and Diagnosis of Toxoplasmosis, California.

出版信息

Open Forum Infect Dis. 2018 Oct 29;5(10):ofy215. doi: 10.1093/ofid/ofy215. eCollection 2018 Oct.

Abstract

BACKGROUND

The cost of conventional serological testing for toxoplasmosis discourages universal adoption of prenatal monthly screening programs to prevent congenital toxoplasmosis. Point-of-care (POC) technology may constitute a cost-effective approach.

METHODS

We evaluated the diagnostic accuracy of 3 POC tests against gold-standard testing performed at Palo Alto Medical Foundation Serology Laboratory (PAMF-TSL). The POC tests included the following: Toxo IgG/IgM Rapid Test (Biopanda) and the OnSite Toxo IgG/IgM Combo-Rapid- that detect IgG and IgM separately, and the Toxoplasma ICT-IgG-IgM- (LDBIO) that detects either or both immunoglobulin IgG/IgM in combination. Samples were selected from PAMF-TSL biobank (n = 210) and Centers for Disease Control and Prevention 1998 Human Serum Panel (n = 100). Based on PAMF-TSL testing, -infection status was classified in 4 categories: acute infections (n = 85), chronic infections (n = 85), false-positive IgM (n = 60), and seronegative (n = 80). The POC testing was performed in duplicate following manufacturer's instructions by investigators blinded to PAMF-TSL results. Sensitivity and specificity were calculated.

RESULTS

A total of 1860 POC tests were performed. For detection of IgG, sensitivity was 100% (170 of 170; 95% confidence interval [CI], 97.8%-100%) for all 3 POC kits; specificity was also comparable at 96.3% (77 of 80; 95% CI, 89.5%-98.9%), 97.5% (78 of 80; 95% CI, 91.3%-99.6%), and 98.8% (79 of 80; 95% CI, 93.2%-99.9%). However, sensitivity for detection of IgM varied significantly across POC tests: Biopanda, 62.2% (51 of 82; 95% CI, 51.4%-71.9%); OnSite, 28% (23 of 82; 95% CI, 19.5%-38.6%); and LDBIO combined IgG/IgM, 100% (82 of 82; 95% CI, 95.5%-100%). Diagnostic accuracy was significantly higher for the LDBIO POC kit. The POC kits did not exhibit cross-reactivity for false-positive -IgM sera.

CONCLUSIONS

The 3 evaluated POC kits revealed optimal sensitivity for -IgG antibodies. The -POC test exhibited 100% sensitivity for the combined detection of IgG/IgM in acute and chronic infection. Biopanda and Onsite POC tests exhibited poor sensitivity for -IgM detection.

摘要

背景

传统的弓形虫病血清学检测成本高昂,这阻碍了普遍采用产前每月筛查计划来预防先天性弓形虫病。即时检测(POC)技术可能是一种具有成本效益的方法。

方法

我们评估了3种POC检测相对于在帕洛阿尔托医学基金会血清学实验室(PAMF - TSL)进行的金标准检测的诊断准确性。POC检测包括:弓形虫IgG/IgM快速检测(Biopanda)和OnSite弓形虫IgG/IgM组合快速检测——分别检测IgG和IgM,以及弓形虫ICT - IgG - IgM检测(LDBIO)——联合检测免疫球蛋白IgG/IgM中的一种或两种。样本选自PAMF - TSL生物样本库(n = 210)和疾病控制与预防中心1998年人类血清样本(n = 100)。根据PAMF - TSL检测,感染状态分为4类:急性感染(n = 85)、慢性感染(n = 85)、IgM假阳性(n = 60)和血清阴性(n = 80)。POC检测由对PAMF - TSL结果不知情的研究人员按照制造商说明重复进行两次。计算敏感性和特异性。

结果

共进行了1860次POC检测。对于IgG检测,所有3种POC试剂盒的敏感性均为100%(170例中的170例;95%置信区间[CI],97.8% - 100%);特异性也相当,分别为96.3%(80例中的77例;95% CI,89.5% - 98.9%)、97.5%(80例中的78例;95% CI,91.3% - 99.6%)和98.8%(80例中的79例;95% CI,93.2% - 99.9%)。然而,不同POC检测对IgM检测的敏感性差异显著:Biopanda为62.2%(82例中的51例;95% CI,51.4% - 71.9%);OnSite为28%(82例中的23例;95% CI,19.5% - 38.6%);LDBIO联合IgG/IgM为100%(82例中的82例;95% CI,95.5% - 100%)。LDBIO POC试剂盒的诊断准确性显著更高。POC试剂盒对假阳性IgM血清未表现出交叉反应性。

结论

所评估的3种POC试剂盒对IgG抗体显示出最佳敏感性。该POC检测对急性和慢性感染中IgG/IgM的联合检测敏感性为100%。Biopanda和OnSite POC检测对IgM检测的敏感性较差。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1267/6204989/78dd36f2fcec/ofy21501.jpg

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