AI Article Synopsis

  • The study evaluates various deconvolution methods that estimate immune cell levels in tumor samples based on gene expression data during a DREAM Challenge.
  • While many established methods perform adequately for most immune cell types, they struggle with accurately assessing all states of functional CD8+ T cells.
  • Community-contributed methods, particularly a deep learning approach, have shown promising results and could enhance the development of deconvolution techniques, especially in identifying functional CD4+ T cell states.

Article Abstract

We evaluate deconvolution methods, which infer levels of immune infiltration from bulk expression of tumor samples, through a community-wide DREAM Challenge. We assess six published and 22 community-contributed methods using in vitro and in silico transcriptional profiles of admixed cancer and healthy immune cells. Several published methods predict most cell types well, though they either were not trained to evaluate all functional CD8+ T cell states or do so with low accuracy. Several community-contributed methods address this gap, including a deep learning-based approach, whose strong performance establishes the applicability of this paradigm to deconvolution. Despite being developed largely using immune cells from healthy tissues, deconvolution methods predict levels of tumor-derived immune cells well. Our admixed and purified transcriptional profiles will be a valuable resource for developing deconvolution methods, including in response to common challenges we observe across methods, such as sensitive identification of functional CD4+ T cell states.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11350143PMC
http://dx.doi.org/10.1038/s41467-024-50618-0DOI Listing

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