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.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 195-200 |
| Number of pages | 6 |
| Journal | Annals of Neurology |
| Volume | 92 |
| Issue number | 2 |
| DOIs | |
| State | Published - Aug 2022 |
Keywords
- Acute-Phase Proteins/metabolism
- Amyotrophic Lateral Sclerosis/metabolism
- Clinical Trials, Phase I as Topic
- Humans
- Inflammation/metabolism
- Oxidative Stress
- T-Lymphocytes, Regulatory/metabolism
ASJC Scopus subject areas
- Clinical Neurology
- Neurology
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