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
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
e0261025Subventions
Organisme : NIAID NIH HHS
ID : U19 AI115658
Pays : United States
Déclaration de conflit d'intérêts
No authors have competing interests.
Références
Emerg Infect Dis. 2011 Sep;17(9):1678-84
pubmed: 21888794
Lancet Infect Dis. 2009 Sep;9(9):524-6
pubmed: 19695489
Cytokine. 2016 Sep;85:80-2
pubmed: 27295614
BMC Infect Dis. 2010 Nov 19;10:332
pubmed: 21087520
Cytokine. 2011 May;54(2):117-20
pubmed: 21316985
PLoS Negl Trop Dis. 2009 Jun 02;3(6):e453
pubmed: 19488407
PLoS Negl Trop Dis. 2007 Oct 31;1(1):e56
pubmed: 17989782
PLoS Negl Trop Dis. 2015 Sep 17;9(9):e0003898
pubmed: 26379143
Crit Care. 2004 Aug;8(4):R204-12
pubmed: 15312219
PLoS Negl Trop Dis. 2014 Jan 16;8(1):e2626
pubmed: 24454971
J Exp Med. 1994 May 1;179(5):1695-9
pubmed: 8163946
BMC Infect Dis. 2020 Apr 7;20(1):268
pubmed: 32264832
Can J Infect Dis Med Microbiol. 2018 Jul 10;2018:9704532
pubmed: 30123395
Jpn J Infect Dis. 2009 Nov;62(6):474-5
pubmed: 19934544
Asian Pac J Trop Med. 2016 Apr;9(4):390-394
pubmed: 27086159
Trans R Soc Trop Med Hyg. 2015 Dec;109(12):749-54
pubmed: 26626338
Indian J Med Microbiol. 2008 Oct-Dec;26(4):405-6
pubmed: 18974510
PLoS Negl Trop Dis. 2013 Sep 19;7(9):e2457
pubmed: 24069500
Mem Inst Oswaldo Cruz. 2015 Jun;110(4):485-91
pubmed: 26061234
Am J Trop Med Hyg. 2011 Sep;85(3):471-8
pubmed: 21896807
Int Arch Med. 2014 Jun 21;7:31
pubmed: 25018781
Eur J Clin Microbiol Infect Dis. 2015 Apr;34(4):687-95
pubmed: 25413923
Trans R Soc Trop Med Hyg. 2015 Nov;109(11):710-6
pubmed: 26464233
PLoS Negl Trop Dis. 2015 Oct 02;9(10):e0004122
pubmed: 26431366
PLoS Negl Trop Dis. 2015 Jun 25;9(6):e0003866
pubmed: 26110270
Am J Trop Med Hyg. 2015 Jan;92(1):139-44
pubmed: 25331809
Clin Infect Dis. 1996 Nov;23(5):1177-8
pubmed: 8922824