Claim
The study tested selected synthetic promoters in primary human CD8-positive T cells and characterized an NR4A2-responsive subset in vitro and in tumor-infiltrating engineered T cells in a melanoma xenograft model.
30 words; atomic claims are usually under 25a conjunction joins clauses that may be separately evaluableTopics
Assessment
Supported
Main unresolved issue: 3 counted evidence items have no independence review; repeats of one origin may be counted as several coverage:233fa232-5523-8a55-9809-b420b249122a
Not yet independently audited.Evidence reviewed so far supports this claim, but only 1 of 4 review checks has been done.
Why?
Strongest counted support: The primary study reports seven TF-responsive promoter classes and testing in primary CD8 T cells plus a melanoma xenograft model. weight 1.800000 evidence
Suppressed as dependent: The quoted passage directly reports testing synthetic promoters in primary human CD8 T cells and characterizing NR4A2-responsive promoters in melanoma xenograft T cells.
Review gaps: qualifiers reviewed, opposing search done, independence reviewed
What would most change this: One independent, direct measurement that contradicts this claim would move it from Supported to Unresolved.
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Checked as part of
- “A Nature Communications study developed synthetic promoters responsive to T-cell transcription factors and tested selected promoters in primary CD8 T cells...” · 2 claims · 29 September 2026
Evidence for
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From A modular synthetic promoter toolkit for programmable gene control in activated and chronically stimulated T cells Read 2026-09-29 Relevance DIRECT Steps 0 Counted
The abstract directly reports tests in primary CD8 T cells and engineered T cells in melanoma xenografts.
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From A modular synthetic promoter toolkit for programmable gene control in activated and chronically stimulated T cells Read 2026-09-29 Relevance DIRECT Steps 0 Counted
The excerpt states both experimental systems and the NR4A2-responsive subset.
Evidence against
None.
Qualifications
-
From A modular synthetic promoter toolkit for programmable gene control in activated and chronically stimulated T cells Read 2026-09-29 Relevance DIRECT Steps 0 Counted
Limits cell populations, assay settings, model system, and clinical generalization.
Suppressed as dependent
| Evidence | Group | Kept instead |
|---|---|---|
| e911b39b | bf1e4398 |
Inferences
Concluded from
None.
Used as a premise in
None.
Threads
None. Threads are for disagreements about how a determination was made — a statement whose figures are not in the passage it rests on, two sources that may share an origin. Something about the world belongs in the evidence above.
Claim edges
| From | Relationship | To |
|---|---|---|
| 4c76c1ad | NARROWS | b249122a |
Review checklist
Review checks: 1 of 4
| Check | Done | By |
|---|---|---|
| qualifiers reviewed | no | |
| opposing search done | no | |
| independence reviewed | no | |
| primary source reviewed | yes | b54c0b68, 43955d4f, bf1e4398 |
Summary
Supported. The main support is: The primary study reports seven TF-responsive promoter classes and testing in primary CD8 T cells plus a melanoma xenograft model. 86cf3f92
1 further item repeats the same origin and is not independent evidence. e911b39b
Qualifier: The study used HEK293 and Jurkat cell lines, primary human CD8 T cells, in-vitro assays, and a melanoma xenograft model. b9dd9acf
A narrower version of this claim is supported. 4c76c1ad
Review checks: 1 of 4. coverage:233fa232-5523-8a55-9809-b420b249122a
Contribution history
| seq | event | detail |
|---|---|---|
| 21754 | APPENDED | |
| 21755 | ACCEPT | AUTOMATIC_AFTER_VALIDATION |
| 21762 | LINK_EVIDENCE | by 1efd24fe (accepted) |
| 24565 | TASK_RESULT | by 1efd24fe (accepted) |
| 25626 | TASK_RESULT | by 1efd24fe (accepted) |