4.5 Article

Pervasive inflammatory activation in patients with deficiency in very-long-chain acyl-coA dehydrogenase (VLCADD)

Journal

CLINICAL & TRANSLATIONAL IMMUNOLOGY
Volume 10, Issue 6, Pages -

Publisher

WILEY
DOI: 10.1002/cti2.1304

Keywords

fatty acid oxidation; inflammation; lymphocytes; monocytes; rhabdomyolysis; very-long-chain acyl-CoA dehydrogenase deficiency

Categories

Funding

  1. United States National Institutes of Health [R01 DK78755]
  2. IRG Award from the Nancy E Taylor Foundation for Chronic Diseases, Inc.

Ask authors/readers for more resources

The study found that patients with VLCADD exhibit systemic inflammatory responses during symptomatic and asymptomatic periods, with an abundance of immune cells expressing high levels of inflammatory mediators. Patients with recurrent hospitalisations showed sustained high levels of plasma cytokines and higher intracellular stores of inflammatory molecules in monocytes.
Objectives. Very-long-chain acyl-CoA dehydrogenase deficiency (VLCADD) is a disorder of fatty acid oxidation. Symptoms are managed by dietary supplementation with medium-chain fatty acids that bypass the metabolic block. However, patients remain vulnerable to hospitalisations because of rhabdomyolysis, suggesting pathologic processes other than energy deficit. Since rhabdomyolysis is a self-destructive process that can signal inflammatory/immune cascades, we tested the hypothesis that inflammation is a physiologic dimension of VLCADD. Methods. All subjects (n = 18) underwent informed consent/assent. Plasma cytokine and cytometry analyses were performed. A prospective case analysis was carried out on a patient with recurrent hospitalisation. Health data were extracted from patient medical records. Results. Patients showed systemic upregulation of nine inflammatory mediators during symptomatic and asymptomatic periods. There was also overall abundance of immune cells with high intracellular expression of IFN gamma, IL-6, MIP-1 beta (CCL4) and TNF alpha, and the transcription factors p65-NF kappa B and STAT1 linked to inflammatory pathways. A case analysis of a patient exhibited already elevated plasma cytokine levels during diagnosis in early infancy, evolving into sustained high systemic levels during recurrent rhabdomyolysis-related hospitalisations. There were corresponding activated leukocytes, with higher intracellular stores of inflammatory molecules in monocytes compared to T cells. Exposure of monocytes to long-chain free fatty acids recapitulated the cytokine signature of patients. Conclusion. Pervasive plasma cytokine upregulation and pre-activated immune cells indicate chronic inflammatory state in VLCADD. Thus, there is rationale for practical implementation of clinical assessment of inflammation and/or translational testing, or adoption, of anti-inflammatory intervention(s) for personalised disease management.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available