mTOR regulates memory CD8 T-cell differentiation
What this study shows
mTOR is a key regulator of memory CD8 T-cell differentiation; rapamycin enhances memory responses.
At a glance
| Evidence type | A Animal model Marked A because it is an animal intervention or observation study measuring an organismal outcome (model: Mouse); the code names the system studied -- animal work can be rigorous and still not be human data. |
| Study type | 4 - Animal Study |
| Model system | Mouse |
| Journal | Nature |
| Year | 2009 |
| Peer reviewed | Yes |
| Record last updated | 2026-10-01 |
| Source | DOI 10.1038/nature08155 · PMID 19543266 · Free full text (PMC2710807) |
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 | Rapamycin (mTOR modulation) |
| Target | mTOR |
| Model | Mouse |
| Effect | mTOR regulates memory CD8 T-cell differentiation; rapamycin enhances memory T-cell quantity and quality |
| Dose | Rapamycin administered continuously (day -1~35), during expansion (days -1~8), or contraction (days 8~35) post-infection; specific quantitative dose not stated. |
| Sample size | not stated |
| Effect size | Rapamycin enhanced LCMV-specific CD8 T cell responses, decreased T cell contraction, and improved functional qualities of memory CD8 T cells. Memory T cell numbers remained 10-fold higher even 165 days after stopping drug treatment, and rapamycin treatment during contraction resulted in significantly higher numbers of functional memory cells (p <0.0001~0.0022). |
| Limitations | mTOR knockdown does not completely mimic rapamycin treatment. |
In the Atlas
Related topics
Open questions that cite this study
- Cited as supporting evidence for the open question Is there a low-dose mTOR schedule whose immune effects come out favourable, compartment by compartment?.
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