Volume 1098, Issue 1 p. 437-445

Rapid Assay Format for Multiplex Detection of Humoral Immune Responses to Infectious Disease Pathogens (HIV, HCV, and TB)

PAUL L. A. M. CORSTJENS

PAUL L. A. M. CORSTJENS

Department of Molecular Cell Biology, Leiden University Medical Center, Leiden, the Netherlands

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ZONGYUANG CHEN

ZONGYUANG CHEN

Department of Mechanical Engineering and Applied Mechanics, University of Pennsylvania, Philadelphia, Pennsylvania, USA

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MICHEL ZUIDERWIJK

MICHEL ZUIDERWIJK

Department of Molecular Cell Biology, Leiden University Medical Center, Leiden, the Netherlands

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HAIM H. BAU

HAIM H. BAU

Department of Mechanical Engineering and Applied Mechanics, University of Pennsylvania, Philadelphia, Pennsylvania, USA

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WILLIAM R. ABRAMS

WILLIAM R. ABRAMS

Department of Basic Sciences, New York University College of Dentistry, New York, New York, USA

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DANIEL MALAMUD

DANIEL MALAMUD

Department of Basic Sciences, New York University College of Dentistry, New York, New York, USA

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R. SAM NIEDBALA

R. SAM NIEDBALA

Department of Chemistry, Lehigh University, Bethlehem, Pennsylvania, USA

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HANS J. TANKE

HANS J. TANKE

Department of Molecular Cell Biology, Leiden University Medical Center, Leiden, the Netherlands

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First published: 02 April 2007
Citations: 76
Address for correspondence: Paul L. A. M. Corstjens, Department of Molecular Cell Biology, Leiden University Medical Center, PO Box 9600, 2300 RC Leiden, the Netherlands. Voice: +31-71-5269209; fax: +31-71-5268270.
[email protected]

Abstract

Abstract: A novel assay is described for multiplex detection of antibodies against different pathogens from a single sample. The assay employs a modified lateral flow format (consecutive flow, CF) together with a sensitive reporter particle technology (up-converting phosphor technology, UPT) that allows for fully instrumented assay analysis. Lateral flow (LF ) strips developed for the detection of human antibodies against human immunodeficiency virus type-1 and -2 (HIV-1 and -2) with additional capture zones to detect antibodies against Myobacterium tuberculosis (TB) and hepatitis C Virus (HCV) provided the strips to test multiplexing. Data are presented that show the performance of the TB and HCV test, as well as two multiplex assays, TB with HIV and HCV with HIV. The TB/HCV assays demonstrate excellent detection capability, and HIV multiplexing does not affect the qualitative test result. The bench-top CF format was converted to a microfluidic platform and a first prototype semiautomated chip capable of performing CF is presented here.