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Study breakdown

T-Cell Activation and Environment Control How Sensitive T-Cells Are to VIP Anti-Inflammatory Peptide

In VitroPreliminary evidence
The takeaway

TCR signaling strength and cytokine environment jointly regulated VPAC-1 receptor expression on CD4 T-cells, determining their sensitivity to VIP's immunomodulatory effects — context-dependent neuropeptide immune regulation.

Key finding

CD4 T-cell VPAC-1 receptor expression was regulated by TCR activation strength and cytokine milieu (IL-2, IL-7, IL-15), determining VIP immunomodulato

What the researchers found

CD4 T-cell VPAC-1 receptor expression was regulated by TCR activation strength and cytokine milieu (IL-2, IL-7, IL-15), determining VIP immunomodulatory sensitivity — explaining context-dependent neuropeptide-immune regulation at the T-cell level.

Why it matters

Relevant for neuropeptides, immune-function.

How the study worked

in-vitro study.

What this study cannot tell us

See abstract.

How to read the evidence

preliminary evidence.

When this study was published

Published in 2008.

The bigger picture

Advances peptide research.

Questions still open

  • Further research needed.
  • Clinical translation to evaluate.

Common questions

What was studied?
T-Cell Activation and Environment Control How Sensitive T-Cells Are to VIP Anti-Inflammatory Peptide
What was found?
TCR signaling strength and cytokine environment jointly regulated VPAC-1 receptor expression on CD4 T-cells, determining their sensitivity to VIP's immunomodulatory effects — context-dependent neuropeptide immune regulation.

Read the original research

TCR signaling and environment affect vasoactive intestinal peptide receptor-1 (VPAC-1) expression in primary mouse CD4 T cells.

Brain, behavior, and immunity, 22(7), 1032-1040

Citation

Vomhof-DeKrey, Emilie E; Hermann, Rebecca J; Palmer, Megan F; Benton, Keith D; Sandy, Ashley R; Dorsam, Sheri T; Dorsam, Glenn Paul. (2008). TCR signaling and environment affect vasoactive intestinal peptide receptor-1 (VPAC-1) expression in primary mouse CD4 T cells.. Brain, behavior, and immunity, 22(7), 1032-1040. https://doi.org/10.1016/j.bbi.2008.04.005