Reliability of a newly-developed immunochromatography diagnostic kit for pandemic influenza A/H1N1pdm virus: implications for drug administration

For the diagnosis of seasonal influenza, clinicians rely on point-of-care testing (POCT) using commercially available kits developed against seasonal influenza viruses. However, POCT has not yet been established for the diagnosis of pandemic influenza A virus (H1N1pdm) infection due to the low sensi...

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Published inPloS one Vol. 7; no. 11; p. e50670
Main Authors Sasaki, Tadahiro, Kubota-Koketsu, Ritsuko, Takei, Michihiro, Hagihara, Tatsuo, Iwamoto, Shinichi, Murao, Takuya, Sawami, Kazuo, Fukae, Daizou, Nakamura, Masahiro, Nagata, Eiichi, Kawakami, Akira, Mitsubayashi, Yuko, Ohno, Masafumi, Uehara, Yasuo, Fukukawa, Takashi, Kanai, Yuta, Kosaka, Mieko, Ikuta, Kazuyoshi
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 30.11.2012
Public Library of Science (PLoS)
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Summary:For the diagnosis of seasonal influenza, clinicians rely on point-of-care testing (POCT) using commercially available kits developed against seasonal influenza viruses. However, POCT has not yet been established for the diagnosis of pandemic influenza A virus (H1N1pdm) infection due to the low sensitivity of the existing kits for H1N1pdm. An immunochromatography (IC) test kit was developed based on a monoclonal antibody against H1N1pdm, which does not cross-react with seasonal influenza A or B viruses. The efficacy of this kit (PDM-IC kit) for the diagnosis of H1N1pdm infection was compared with that of an existing kit for the detection of seasonal influenza viruses (SEA-IC kit). Nasal swabs (n = 542) were obtained from patients with flu-like syndrome at 13 clinics in Osaka, Japan during the winter of 2010/2011. Among the 542 samples, randomly selected 332 were further evaluated for viral presence by reverse transcriptase polymerase chain reaction (RT-PCR). The PDM-IC kit versus the SEA-IC kit showed higher sensitivity to and specificity for H1N1pdm, despite several inconsistencies between the two kits or between the kits and RT-PCR. Consequently, greater numbers of false-negative and false-positive cases were documented when the SEA-IC kit was employed. Significant correlation coefficients for sensitivity, specificity, and negative prediction values between the two kits were observed at individual clinics, indicating that the results could be affected by clinic-related techniques for sampling and kit handling. Importantly, many patients (especially influenza-negative cases) were prescribed anti-influenza drugs that were incongruous with their condition, largely due to physician preference for patient responses to questionnaires and patient symptomology, as opposed to actual viral presence. Concomitant use of SEA-IC and PDM-IC kits increased the likelihood of correct influenza diagnosis. Increasing the credibility of POCT is anticipated to decrease the inappropriate dispensing of anti-influenza drugs, thereby minimizing the emergence of drug-resistant H1N1pdm strains.
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Competing Interests: Tadahiro Sasaki is responsible for recognizing and disclosing on behalf of all authors any competing interest that could be perceived to bias their work, acknowledging all financial support and any other relevant financial or competing interests. Mieko Kosaka is employed by Alfresa Pharma Corporation. Funding for collaboration research was from this company only to Osaka University under the contract between Alfresa Pharma Corporation and Osaka University, but not to the authors. Also, immunochromatography kits, products of this company, were supported by this company for this study. The authors declare that they have no affiliations to this company, along with any other relevant declarations relating to employment, consultancy, patents, products, products in development or marketed products. This does not alter the authors’ adherence to all the PLOS One policies on sharing data and materials.
Conceived and designed the experiments: TS RKK MT MK KI. Performed the experiments: TS RKK. Analyzed the data: TS RKK MK. Contributed reagents/materials/analysis tools: MT TH SI TM KS DF MN EN AK YM MO YU TF. Wrote the paper: TS SK KI. Edited the manuscript: RKK SK MK YK. Provided oversight, support, and recruitment of study participants, as well as sample management: MT MK.
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0050670