A novel method to compensate for different amplification efficiencies between patient DNA samples in quantitative real-time PCR

J Meijerink, C Mandigers, L van de Locht… - The Journal of Molecular …, 2001 - Elsevier
J Meijerink, C Mandigers, L van de Locht, E Tönnissen, F Goodsaid, J Raemaekers
The Journal of Molecular Diagnostics, 2001Elsevier
Quantification of residual disease by real-time polymerase chain reaction (PCR) will become
a pivotal tool in the development of patient-directed therapy. In recent years, various
protocols to quantify minimal residual disease in leukemia or lymphoma patients have been
developed. These assays assume that PCR efficiencies are equal for all samples.
Determining t (14; 18) and albumin reaction efficiencies for sixteen follicular lymphoma
patient samples revealed higher efficiencies for blood samples than for lymph node samples …
Quantification of residual disease by real-time polymerase chain reaction (PCR) will become a pivotal tool in the development of patient-directed therapy. In recent years, various protocols to quantify minimal residual disease in leukemia or lymphoma patients have been developed. These assays assume that PCR efficiencies are equal for all samples. Determining t(14;18) and albumin reaction efficiencies for sixteen follicular lymphoma patient samples revealed higher efficiencies for blood samples than for lymph node samples in general. However, within one sample both reactions had equivalent efficiencies. Differences in amplification efficiencies between patient samples (low efficiencies) and the calibrator in quantitative analyses result in the underestimation of residual disease in patient samples whereby the weakest positive patient samples are at highest error. Based on these findings for patient samples, the efficiency compensation control was developed. This control includes two reference reactions in a multiplex setting, specific for the β-actin and albumin housekeeping genes that are present in a constant ratio within DNA templates. The difference in threshold cycle values for both reference reactions, ie, the ΔCt2value, is dependent on the amplification efficiency, and is used to compensate for efficiency differences between patient samples and the calibrator. The β-actin reference reaction is also used to normalize for DNA input. Furthermore, the efficiency compensation control facilitates identification of patient samples that are so contaminated with PCR inhibitory compounds that different amplification reactions are affected to a different extent. Accurate quantitation of residual disease in these samples is therefore impossible with the current quantitative real-time PCR protocols. Identification and exclusion of these inadequate samples will be of utmost importance in quantitative retrospective studies, but even more so, in future molecular diagnostic analyses.
Elsevier