AI Article Synopsis

  • The rat protoparvovirus H-1 (H-1PV) is known for its anticancer effects in human tumors, particularly non-Hodgkin lymphomas (NHL), but its impact on T-cell malignancies has been less studied.
  • A pilot study showed that H-1PV successfully infected and induced cancer cell death in cutaneous T-cell lymphoma (CTCL) models, while not affecting healthy cells, and even increased immune cell infiltration in cancer spheroids.
  • The findings suggest that H-1PV could be a promising new treatment option for CTCL, highlighting its potential as a viroimmunotherapeutic candidate.

Article Abstract

The rat protoparvovirus H-1 (H-1PV) is an oncolytic virus known for its anticancer properties in laboratory models of various human tumors, including non-Hodgkin lymphomas (NHL) of B-cell origin. However, H-1PV therapeutic potential against hematological malignancies of T-cell origin remains underexplored. The aim of the present study was to conduct a pilot preclinical investigation of H-1PV-mediated oncolytic effects in cutaneous T-cell lymphoma (CTCL), a type of NHL that is urgently calling for innovative therapies. We demonstrated H-1PV productive infection and induction of oncolysis in both classically grown CTCL suspension cultures and in a novel, in vivo-relevant, heterotypic spheroid model, but not in healthy donor controls, including peripheral blood mononuclear cells (PBMCs). H-1PV-mediated oncolysis of CTCL cells was not prevented by Bcl-2 overexpression and was accompanied by increased extracellular ATP release. In CTCL spheroid co-cultures with PBMCs, increased spheroid infiltration with immune cells was detected upon co-culture treatment with the virus. In conclusion, our preclinical data show that H-1PV may hold significant potential as an ingenious viroimmunotherapeutic drug candidate against CTCL.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11311363PMC
http://dx.doi.org/10.3390/cancers16152711DOI Listing

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