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Tregs Attenuate Peripheral Oxidative Stress and Acute Phase Proteins in ALS. | LitMetric

Tregs Attenuate Peripheral Oxidative Stress and Acute Phase Proteins in ALS.

Ann Neurol

Peggy and Gary Edwards ALS Laboratory, Department of Neurology, Houston Methodist Neurological Institute, Houston Methodist Research Institute, Houston Methodist Hospital, Houston, Texas, USA.

Published: August 2022

AI Article Synopsis

  • Oxidative stress (OS) triggers inflammation that worsens OS and increases acute phase proteins (APPs), impacting conditions like amyotrophic lateral sclerosis (ALS).
  • A phase I clinical trial with regulatory T lymphocyte (Treg) therapy showed that the treatment could reduce levels of oxidized low-density lipoprotein (ox-LDL) during administration, but these levels increased when therapy ceased.
  • Additionally, while Treg therapy stabilized various inflammatory markers, these markers rose when treatment stopped, indicating that Treg therapy might help manage oxidative stress and inflammation, offering a way to monitor the effectiveness of immunomodulating therapies.

Article Abstract

Oxidative stress (OS) induces inflammation, which in turn exacerbates OS and the expression of acute phase proteins (APPs). Regulatory T lymphocyte (Treg) therapy was assessed for suppression of OS and APP responses in longitudinal serum samples from subjects with amyotrophic lateral sclerosis (ALS) enrolled in a phase I clinical trial. The first round of Treg therapy suppressed levels of oxidized low-density lipoprotein (ox-LDL). During a 6-month washout period, ox-LDL levels increased. A second round of therapy again suppressed ox-LDL levels and then rose following the cessation of treatment. Serum levels of APPs, soluble CD14, lipopolysaccharide binding protein, and C-reactive protein, were stabilized during Treg administrations, but rose during the washout period and again after therapy was discontinued. Treg therapy potentially suppresses peripheral OS and the accompanying circulating pro-inflammatory induced APPs, both of which may serve as peripheral candidates for monitoring efficacies of immunomodulating therapies. ANN NEUROL 2022;92:195-200.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545429PMC
http://dx.doi.org/10.1002/ana.26375DOI Listing

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