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Updated: Jun 2, 2026

Development and Validation of an Ultrasensitive Single Molecule Array Digital Enzyme-linked Immunosorbent Assay for Human Interferon-α
Published on: June 14, 2018
Immuno-PCR: a promising ultrasensitive diagnostic method to detect antigens and antibodies
1URMITE CNRS/IRD 6236, Faculté de médecine, Université de la Méditerranée, Marseille, 13385, France.
Insights
Immuno-PCR (iPCR) combines ELISA and PCR for sensitive protein detection. Recent advancements are making iPCR a viable and routine tool for microbial diagnostics.
Area of Science:
- Biotechnology
- Immunology
- Molecular Biology
Background:
- Immuno-PCR (iPCR) merges ELISA and PCR, offering high sensitivity for protein antigen detection.
- Historically, iPCR has been underutilized due to limitations, reflected in sparse publication records.
- The development of novel systems and reagents is enhancing iPCR's applicability.
Purpose of the Study:
- To review the evolution of Immuno-PCR (iPCR) technology.
- To highlight the advancements that address previous drawbacks of iPCR.
- To explore the potential of iPCR as a routine microbial diagnostic tool.
Main Methods:
- Review of classical and modern Immuno-PCR (iPCR) formats.
- Analysis of technological improvements in iPCR systems.
- Evaluation of iPCR's suitability for microbial diagnostics.
Main Results:
- Early iPCR formats presented significant drawbacks hindering routine use.
- Modern iPCR systems incorporate ready-to-use reagents and diverse linker molecules.
- Protocol times have been reduced, and new systems enhance iPCR's practicality.
Conclusions:
- Immuno-PCR (iPCR) has evolved from a niche technique to a promising diagnostic method.
- Technological refinements are overcoming previous limitations of iPCR.
- iPCR is poised to become an essential tool in microbial diagnostics.
Abstract:
Immuno-PCR (iPCR) is a method that combines the advantages of both enzyme-linked immunosorbent assay and PCR and is a powerful method for detecting low quantities of protein antigens. Despite its potential, for a long time iPCR was an underutilized method as evidenced by the low number of publications on its routine application. The introduction of ready-to-use reagents, the large choice in linker molecule, reduction of protocol time and the development of new systems is opening the way for iPCR to become a routine method for use as a microbial diagnostic. To understand how iPCR could become an indispensible microbial diagnostic, we review the evolution of iPCR, from its first classical format with numerous drawbacks to more sophisticated systems developed to circumvent these drawbacks.
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