mTORC1 inhibition upregulates CD20 and enhances anti-CD20 antibody efficacy in B-cell precursor acute lymphoblastic leukemia
What this study shows
mTORC1 inhibitors upregulate CD20 via the AKT-FOXO1 axis and promote B-lineage maturation in B-cell precursor ALL, enhancing the antitumor efficacy of anti-CD20 monoclonal antibodies -- including in high-risk IKZF1-deleted disease -- providing a rationale for combining mTORC1 inhibition with CD20-directed immunotherapy.
At a glance
| Evidence type | M Molecular — cells, biochemistry, structure Marked M because it is molecular or in-vitro work (model: BCP-ALL cell lines; patient-derived and in vivo models) rather than a whole-organism health-outcome study. That is often exactly where causal biology gets established -- the code says which system the finding was shown in, and nothing about how good the work is. |
| Study type | 5 - Mechanistic / In Vitro |
| Model system | BCP-ALL cell lines; patient-derived and in vivo models |
| Journal | Leukemia |
| Year | 2026 |
| Peer reviewed | Yes |
| Record last updated | 2026-10-01 |
| Source | DOI 10.1038/s41375-026-03093-z · PMID 42618701 |
Extracted findings
These fields were extracted from the paper with AI assistance and have not been checked against the source. Read them as a pointer into the paper, not as curated claims; where they disagree with the curated summary above, the curated summary stands.
| Intervention | mTORC1 inhibitors; wild-type IKZF1 overexpression; anti-CD20 monoclonal antibody combination |
| Target | mTORC1, with CD20 induction via the AKT-FOXO1 axis |
| Model | human BCP-ALL cell lines, patient-derived models and in vivo models |
| Effect | mTORC1 inhibition raised CD20 and promoted B-lineage maturation, improving anti-CD20 antibody efficacy including in IKZF1-deleted models. |
In the Atlas
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