Transcriptomics

Dataset Information

0

Serum Inflammatory Mediators as Markers of Human Lyme Disease Activity


ABSTRACT: Chemokines and cytokines are key signaling molecules that orchestrate the trafficking of immune cells, direct them to sites of tissue injury and inflammation and modulate their states of activation and effector cell function. We have measured, using a multiplex-based approach, the levels of 58 immune mediators and 7 acute phase markers in sera derived from of a cohort of patients diagnosed with acute Lyme disease and matched controls. This analysis identified a cytokine signature associated with the early stages of infection and allowed us to identify two subsets (mediator-high and mediator-low) of acute Lyme patients with distinct cytokine signatures that also differed significantly (p<0.0005) in symptom presentation. In particular, the T cell chemokines CXCL9 (MIG), CXCL10 (IP-10) and CCL19 (MIP3B) were coordinately increased in the mediator-high group and levels of these chemokines could be associated with seroconversion status and elevated liver function tests (p=0.027 and p=0.021 respectively). There was also upregulation of acute phase proteins including CRP and serum amyloid A. Consistent with the role of CXCL9/CXCL10 in attracting immune cells to the site of infection, CXCR3+ CD4 T cells are reduced in the blood of early acute Lyme disease (p=0.01) and the decrease correlates with chemokine levels (p=0.0375). The levels of CXCL9/10 did not relate to the size or number of skin lesions but elevated levels of serum CXCL9/CXCL10 were associated with elevated liver enzymes levels. Collectively these results indicate that the levels of serum chemokines and the levels of expression of their respective chemokine receptors on T cell subsets may prove to be informative biomarkers for Lyme disease and related to specific disease manifestations. A total of 65 immune and inflammatory mediators were profiled in serum samples derived from early Lyme disease patients and age- and sex-matched controls. These samples have been generated as part of a prospective cohort study that includes a well-defined cohort of patients with acute Lyme disease enrolled from a Lyme endemic area of the mid-Atlantic United States. Only patients with untreated, confirmed early Lyme disease manifesting an active EM skin lesion at the time of enrollment, as defined by CDC case criteria are eligible. Patients with a history of prior Lyme disease or the presence of confounding preexisting medical conditions associated with prolonged fatigue, pain or neurocognitive symptoms are excluded. Controls are nonhospitalized age- and sex-matched and have no prior history of Lyme disease or any exclusionary medical conditions including lack of inflammatory disorders.

ORGANISM(S): Homo sapiens  

SUBMITTER: Lauren A Crowder   Mark J Soloski  William H Robinson  Lauren J Lahey  Catriona A Wagner  John N Aucott  William Robinson 

PROVIDER: E-GEOD-55815 | ArrayExpress | 2014-04-25

SECONDARY ACCESSION(S): GSE55815PRJNA241073

REPOSITORIES: GEO, ArrayExpress

altmetric image

Publications

Serum inflammatory mediators as markers of human Lyme disease activity.

Soloski Mark J MJ   Crowder Lauren A LA   Lahey Lauren J LJ   Wagner Catriona A CA   Robinson William H WH   Aucott John N JN  

PloS one 20140416 4


Chemokines and cytokines are key signaling molecules that orchestrate the trafficking of immune cells, direct them to sites of tissue injury and inflammation and modulate their states of activation and effector cell function. We have measured, using a multiplex-based approach, the levels of 58 immune mediators and 7 acute phase markers in sera derived from of a cohort of patients diagnosed with acute Lyme disease and matched controls. This analysis identified a cytokine signature associated with  ...[more]

Similar Datasets

2008-06-14 | E-GEOD-6092 | ArrayExpress
| GSE84479 | GEO
| GSE80805 | GEO
2016-02-15 | E-GEOD-63085 | ArrayExpress
2018-06-24 | GSE113770 | GEO
| GSE79741 | GEO
2012-11-19 | E-GEOD-36331 | ArrayExpress
| GSE97835 | GEO
2008-08-30 | GSE12627 | GEO
2008-10-25 | E-GEOD-12627 | ArrayExpress