AI Article Synopsis

  • The sympathetic nervous system (SNS) influences immune cell functions, playing a dual role in promoting tumor growth while potentially impairing antitumor immunity.
  • Recent findings indicate that norepinephrine affects cytokine production in monocyte-derived macrophages, but dendritic cells do not respond to it due to a lack of β-adrenergic receptor expression.
  • Combining the β-blocker propranolol with a peptide cancer vaccine significantly improved DC maturation, increased effective CD8 T cell presence in tumors, reduced suppressor cell levels, and resulted in a notable reduction in tumor growth compared to the vaccine alone.

Article Abstract

The sympathetic nervous system (SNS) is an important regulator of immune cell function during homeostasis and states of inflammation. Recently, the SNS has been found to bolster tumor growth and impair the development of antitumor immunity. However, it is unclear whether the SNS can modulate APC function. Here, we investigated the effects of SNS signaling in murine monocyte-derived macrophages (moMФ) and dendritic cells (DCs) and further combined the nonspecific β-blocker propranolol with a peptide cancer vaccine for the treatment of melanoma in mice. We report that norepinephrine treatment dramatically altered moMФ cytokine production, whereas DCs were unresponsive to norepinephrine and critically lack β-adrenergic receptor expression. In addition, we show that propranolol plus cancer vaccine enhanced peripheral DC maturation, increased the intratumor proportion of effector CD8 T cells, and decreased the presence of intratumor PD-L1 myeloid-derived suppressor cells. Furthermore, this combination dramatically reduced tumor growth compared with vaccination alone. Taken together, these results offer insights into the cell-specific manner by which the SNS regulates the APC immune compartment and provide strong support for the use of propranolol in combination with cancer vaccines to improve patient response rates and survival.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9583274PMC
http://dx.doi.org/10.4049/jimmunol.2100719DOI Listing

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