Clinical spectrum of endemic leptospirosis in relation to cytokine response.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2021
Historique:
received: 19 09 2021
accepted: 22 11 2021
entrez: 8 12 2021
pubmed: 9 12 2021
medline: 7 1 2022
Statut: epublish

Résumé

To describe the clinical spectrum and the cytokine response of leptospirosis patients in an endemic setting of Sri Lanka. Patients presenting to the university teaching hospital, Anuradhapura, Sri Lanka with a leptospirosis-compatible illness were recruited over a period of 12 months starting from June 2012. Daily clinical and biochemical parameters of the patients were prospectively assessed with a follow-up of 14 days after discharge. A magnetic bead-based multiplex cytokine kit was used to detect 17 cytokines. Of the 142 clinically suspected leptospirosis patients recruited, 47 were confirmed and, 29 cases were labeled as "probable." Thrombocytopenia and leukocytosis were observed at least once during the hospital stay among 76(54%) and 39(28%) patients, respectively. Acute kidney injury was observed in 31 patients (22%) and it was significantly higher among confirmed and probable cases. Hu TNF-α and IL-1β were detected only in patients without complications. Hu MIP-1b levels were significantly higher among patients with complications. During the convalescence period, all tested serum cytokine levels were lower compared to the acute sample, except for IL-8. The cytokine response during the acute phase clustered in four different groups. High serum creatinine was associated GM-CSF, high IL-5 and IL-6 level were correlates with lung involvement and saturation drop. The patients with high billirubin (direct)>7 mmol/l had high IL-13 levels. Results of this study confirms that the knowledge on cytokine response in leptospirosis could be more complex than other similar tropical disease, and biosignatures that provide diagnostic and prognostic information for human leptospirosis remain to be discovered.

Identifiants

pubmed: 34879100
doi: 10.1371/journal.pone.0261025
pii: PONE-D-21-30348
pmc: PMC8654203
doi:

Substances chimiques

Biomarkers 0
Cytokines 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0261025

Subventions

Organisme : NIAID NIH HHS
ID : U19 AI115658
Pays : United States

Déclaration de conflit d'intérêts

No authors have competing interests.

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Auteurs

Niroshana J Dahanayaka (NJ)

Faculty of Medicine and Allied Sciences, Department of Medicine, Rajarata University of Sri Lanka, Saliyapura, Sri Lanka.
Faculty of Medicine, Department of Medicine, University of Ruhuna, Matara, Sri Lanka.

Suneth B Agampodi (SB)

Department of Internal Medicine, Section of Infectious Diseases, School of Medicine, Yale University, New Haven, Connecticut, United States of America.
Faculty of Medicine and Allied Sciences, Department of Community Medicine, Rajarata University of Sri Lanka, Saliyapura, Sri Lanka.

Indika Seneviratna (I)

Faculty of Medicine and Allied Sciences, Department of Biochemistry, Rajarata University of Sri Lanka, Saliyapura, Sri Lanka.

Janith Warnasekara (J)

Faculty of Medicine and Allied Sciences, Department of Community Medicine, Rajarata University of Sri Lanka, Saliyapura, Sri Lanka.

Rukman Rajapakse (R)

Faculty of Medicine and Allied Sciences, Department of Medicine, Rajarata University of Sri Lanka, Saliyapura, Sri Lanka.

Kosala Ranathunga (K)

Faculty of Medicine and Allied Sciences, Department of Medicine, Rajarata University of Sri Lanka, Saliyapura, Sri Lanka.

Michael Matthias (M)

Department of Internal Medicine, Section of Infectious Diseases, School of Medicine, Yale University, New Haven, Connecticut, United States of America.

Joseph M Vinetz (JM)

Department of Internal Medicine, Section of Infectious Diseases, School of Medicine, Yale University, New Haven, Connecticut, United States of America.

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