Volume 64, Issue 1 pp. 57-60
Research Article

Developing a new clinical tool for diagnosing chronic Q fever: the Coxiella ELISPOT

Gijs J.M. Limonard

Corresponding Author

Gijs J.M. Limonard

Department of Pulmonary Diseases, Diakonessenhuis Utrecht, Utrecht, The Netherlands

Correspondence: Gijs J.M. Limonard, MD, Department of Pulmonary Diseases, Diakonessenhuis Utrecht, Bosboomstraat 1, 3508 TG Utrecht, The Netherlands. Tel.: 0031 88 2506445; fax: +31 88 2506673; e-mail: [email protected]Search for more papers by this author
Steven F. Thijsen

Steven F. Thijsen

Department of Medical Microbiology & Immunology, Diakonessenhuis Utrecht, Utrecht, The Netherlands

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Aik W. Bossink

Aik W. Bossink

Department of Pulmonary Diseases, Diakonessenhuis Utrecht, Utrecht, The Netherlands

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Anita Asscheman

Anita Asscheman

Department of Medical Microbiology & Immunology, Diakonessenhuis Utrecht, Utrecht, The Netherlands

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John J.M. Bouwman

John J.M. Bouwman

Department of Medical Microbiology & Immunology, Diakonessenhuis Utrecht, Utrecht, The Netherlands

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First published: 03 November 2011
Citations: 2

Abstract

Definitively establishing a clinical diagnosis of chronic Q fever remains challenging, as the diagnostic performance of both conventional serological tests and PCR is limited. Given the importance of an early diagnosis of chronic Q fever, there is a need for a reliable diagnostic test. We developed an enzyme-linked immunospot assay to measure Coxiella burnetii (C. burnetii)-specific T-cell responses (Coxiella ELISPOT) to both phase I and phase II antigens and tested convalescent Q fever patients (without chronic disease, n = 9) and patients with an established diagnosis of chronic Q fever (n = 3). The Coxiella ELISPOT adequately identified convalescent Q fever patients from healthy controls by demonstrating C. burnetii-specific T-cell interferon-γ production to both phase I and phase II antigens. Compared to convalescent Q fever patients, chronic Q fever patients showed a distinct Coxiella ELISPOT profile characterized by a much higher spot count for both phase I and phase II (18-fold for phase II, 8-fold higher for phase I) and a consistent shift towards more phase I reactivity. The diagnostic potential of the Coxiella ELISPOT is promising and warrants further investigation.

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