Standardized, mathematical model-based and validated in vitro analysis of anthrax lethal toxin neutralization

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• 作者：Han Li ; Stephen D. Soroka ; Thomas H. Taylor Jr. ; Karen L. Stamey ; Kelly Wallace Stinson ; Alison E. Freeman ; Darbi R. Abramson ; Rita Desai ; Li X. Cronin ; J. Wade Oxford ; Joseph Caba ; Cynthia Pleatman
• 关键词：Anthrax toxin ; Neutralization ; Validation ; 4 Parameter logistic ; Standardization ; Antibody
• 刊名：Journal of Immunological Methods
• 出版年：2008
• 期刊代码：57_00221759
• 类别：imm
• 出版时间：20 April 2008
• 卷：333
• 期：1-2
• 页码：89-106
• 文件大小：597 K

摘要

Quantification of anthrax lethal toxin (LTx) neutralization activity (TNA) is pivotal in assessing protective antibody responses to anthrax vaccines and for evaluation of immunotherapies for anthrax. We have adapted and redesigned the TNA assay to establish a unifying, standardized, quantitative and validated technology platform for LTx neutralization in the J774A.1 murine cell line. Critical design features of this platform are 1) the application of a free-form or constrained 4 parameter logistic (4-PL) function to model neutralization responses within and between boundary limits of 100%cell survival and 95%cell lysis and 2) to exploit innovative assay curve recognition algorithms for interpretive endpoints. The assay was validated using human serum ED50 (dilution of serum effecting 50%neutralization) as the primary reportable value (RV). Intra-operator and intermediate precision, expressed as the coefficient of variation (%CV), were high at 10.5–15.5%CV and 13.5–14.5%CV respectively. TNA assay dilutional linearity was demonstrated for human sera using linear regression analysis of log₁₀ transformed data with slope = 0.99, intercept = − 0.03 and r² = 0.985. Assay accuracy, inferred from the precision and linearity data and using a spike-recovery approach, was high with a percent error (%E) range of only 3.4–20.5%E. The lower limit of detection (LLOD) was ED50 = 12 and the lower limit of quantification (LLOQ) was ED50 = 36. The cell-based assay was robust, tolerating incubation temperatures from 35 to 39 °C, CO₂ concentrations from 3%to 7%and reporter substrate (MTT) concentrations of 2.5–7.5 mg/ml. Strict assay quality control parameters were met for up to 25 cell culture passages. The long term (50 month) assay stability, determined using human reference standards AVR414 and AVR801, indicated high precision, consistent accuracy and no detectable assay drift. A customized software program provided two additional assay metrics, Quantification Titer (QT) and Threshold Titer (TT), both of which demonstrate acceptable accuracy, precision and dilutional linearity. The TT was also used to establish the assay reactivity threshold (RT). The application of the assay to sera from humans, Rhesus macaques and rabbits was demonstrated separately and by aggregate dilutional linearity analysis of the ED50 (slope = 0.98, intercept = 0.003, r² = 0.989). We propose this TNA assay format with a qualified standard reference serum and customized interpretive software as a unifying platform technology for determination of functional serologic responses to anthrax vaccines and for evaluation of anthrax immunotherapeutics.