AI Article Synopsis

  • Cancer immunotherapy shows promise for treating cancer with low toxicity, but many patients don't respond effectively to it alone.
  • This study explores a combination treatment using adoptive cell therapy (ACT) with photothermal therapy (PTT), employing smart gold nanoparticles (sAuNPs) to enhance the effectiveness of T cells against tumors.
  • The results indicate that while the T cells can infiltrate tumors and initially control growth, the tumors eventually regrow; thus, combining ACT with PTT leads to significantly better outcomes compared to using either treatment on its own.

Article Abstract

Cancer immunotherapy is a promising therapy to treat cancer patients with minimal toxicity, but only a small fraction of patients responded to it as a monotherapy. In this study, a strategy to boost therapeutic efficacy by combining an immunotherapy based on ex vivo expanded tumor-reactive T cells is devised, or adoptive cell therapy (ACT), with photothermal therapy (PTT). Smart gold nanoparticles (sAuNPs), which aggregates to form gold nanoclusters in the cells, are loaded into T cells, and their photothermal effects within T cells are confirmed. When transferred into tumor-bearing mice, large number of sAuNP-carrying T cells successfully infiltrate into tumor tissues and exert anti-tumor activity to suspend tumor growth, but over time tumor cells evade and regrow. Of note, ≈20% of injected doses of sAuNPs are deposited in tumor tissues, suggesting T cells are an efficient nanoparticle tumor delivery vehicle. When T cells no longer control tumor growth, PTT is performed to further eliminate tumors. In this manner, ACT and PTT are temporally coupled, and the combined immuno-photothermal treatment demonstrated significantly greater therapeutic efficacy than the monotherapy.

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Source
http://dx.doi.org/10.1002/smll.202301377DOI Listing

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