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总肺炎球菌多糖反应在原发性体液免疫缺陷诊断中的价值

Value of the Overall Pneumococcal Polysaccharide Response in the Diagnosis of Primary Humoral Immunodeficiencies.

作者信息

Lopez Benjamin, Bahuaud Mathilde, Fieschi Claire, Mehlal Souad, Jeljeli Mohamed, Rogeau Stéphanie, Brabant Séverine, Deleplancque Anne-Sophie, Dubucquoi Sylvain, Poizot Sandrine, Terriou Louis, Launay David, Batteux Frédéric, Labalette Myriam, Lefèvre Guillaume

机构信息

CHU Lille, Institut d'Immunologie, Lille, France.

Univ. Lille, U995 - LIRIC - Lille Inflammation Research International Center, Lille, France.

出版信息

Front Immunol. 2017 Dec 20;8:1862. doi: 10.3389/fimmu.2017.01862. eCollection 2017.

Abstract

BACKGROUND

An overall response assay [OVA, based on a 23-valent pneumococcal polysaccharide vaccine (PPV23)] is widely used to screen for anti-pneumococcal antibodies. Given the heterogeneity of response from one polysaccharide (PS) to another, a World Health Organization-standardized serotype-specific enzyme-linked immunosorbent assay (SSA) is considered to be the only reliable method for testing anti-PS antibody responses in individuals with suspected primary immunodeficiencies (PIDs).

OBJECTIVE

To evaluate the OVA relative to the reference SSA.

METHODS

Serum samples of adult patients referred for a suspected PID were collected before and then 4-8 weeks after immunization with PPV23. The anti-pneumococcal response was systematically assessed with an SSA (7-16 serotypes) and interpreted according to the American Academy of Asthma, Allergy and Immunology's current guidelines. We used receiver operating characteristic curves and agreement indices to assess the OVA's diagnostic value in a first cohort. In order to validate these findings, a second (validation) cohort was then prospectively included.

RESULTS

Sixty-two adult patients were included, and 42 (67.7%) were defined as poor responders according to the SSA. Only the post-immunization titer in the OVA was able to correctly identify poor responders; a titer below 110 mg/L gave a positive predictive value of 100% [identifying 24 (57.1%) of the 42 poor responders], and similar levels of diagnostic performance were observed in the validation cohort. The pre-vaccination antibody titer, the post/pre-vaccination antibody titer ratio and a post-vaccination titer above 110 mg/L in the OVA were not predictive of the response in the SSA.

CONCLUSION

A post-vaccination antibody titer below 110 mg/L in the OVA was constantly associated with a poor PPV23 response using the SSA. In all other cases, SSA is the only reliable method for assessing diagnostic vaccination with PPV23.

摘要

背景

一种总体反应检测方法[基于23价肺炎球菌多糖疫苗(PPV23)的OVA]被广泛用于筛查抗肺炎球菌抗体。鉴于不同多糖(PS)之间反应的异质性,世界卫生组织标准化的血清型特异性酶联免疫吸附测定(SSA)被认为是检测疑似原发性免疫缺陷(PID)个体抗PS抗体反应的唯一可靠方法。

目的

相对于参考SSA评估OVA。

方法

收集因疑似PID转诊的成年患者血清样本,在接种PPV23前及接种后4 - 8周采集。用SSA(7 - 16种血清型)系统评估抗肺炎球菌反应,并根据美国哮喘、过敏和免疫学会的现行指南进行解读。我们使用受试者操作特征曲线和一致性指数评估OVA在第一个队列中的诊断价值。为了验证这些发现,随后前瞻性纳入了第二个(验证)队列。

结果

纳入62例成年患者,根据SSA,42例(67.7%)被定义为低反应者。只有OVA中接种后的滴度能够正确识别低反应者;滴度低于110mg/L时,阳性预测值为100%[识别出42例低反应者中的24例(57.1%)],在验证队列中观察到类似水平的诊断性能。OVA中接种前抗体滴度、接种前/后抗体滴度比值以及接种后滴度高于110mg/L均不能预测SSA中的反应。

结论

OVA中接种后抗体滴度低于110mg/L与使用SSA时PPV23反应不佳始终相关。在所有其他情况下,SSA是评估PPV23诊断性接种的唯一可靠方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a59/5742330/cb440c2fab33/fimmu-08-01862-g001.jpg

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