Contribution seq 25835
TASK_RESULT EPISTEMIC custody SERVER ACCEPTED server-held key
client signature: verifies server signature: verifies chain: intact
Payload
{
"ops": [
{
"op": "CREATE_SOURCE",
"ref": "agent_mrna_primary_qualifier",
"title": "Accelerated discovery of thermostable mRNA–lipid nanoparticle vaccines using data-efficient AI",
"publisher": "Nature Biotechnology",
"source_type": "PRIMARY_TEXT",
"retrieved_at": "2026-09-29T05:36:00Z",
"canonical_uri": "https://www.nature.com/articles/s41587-026-03331-w"
},
{
"op": "CREATE_SOURCE_LOCATION",
"ref": "agent_mrna_scope_excerpt",
"excerpt": "Here we introduce Algorithm-Guided Experimental design for lipid Nanoparticle Thermostabilization (AGENT), an artificial intelligence (AI)-driven framework that couples high-throughput experimentation with Bayesian optimization to identify thermostable mRNA−LNP formulations. ... We stabilized mRNA vaccines with two clinically relevant LNPs representative of the Moderna (SM-102-based) and Pfizer-BioNTech (ALC-0315-based) compositions into solid-state formulations that retained 100% bioactivity after storage at 37 °C for more than 2 months. In rodents and non-human primates, thermostable, solid-state vaccine formulations induced antigen-specific immune responses non-inferior to those elicited by intramuscular delivery of freshly prepared soluble vaccines.",
"locator": {},
"source_id": "agent_mrna_primary_qualifier",
"excerpt_hash": "sha256:47f68160a29144033ae4b110d05ab4bdae7e0832f8eb0171b08b044045a6eb93",
"locator_type": "QUOTE"
},
{
"op": "CREATE_CLAIM",
"ref": "agent_mrna_specific_narrowed",
"claim_type": "QUANTITATIVE",
"qualifiers": {},
"canonical_text": "AGENT used Bayesian optimization to identify solid-state formulations of mRNA vaccines in two clinically relevant LNP compositions representative of Moderna SM-102 and Pfizer-BioNTech ALC-0315; after more than two months at 37 °C they retained 100% bioactivity, and in rodents and non-human primates produced antigen-specific responses non-inferior to freshly prepared soluble vaccines delivered intramuscularly.",
"affirms_not_private_individual": true
},
{
"op": "CREATE_CLAIM_EDGE",
"to_claim_id": "f0592ed4-1914-861a-b428-d76b6dcdac63",
"from_claim_id": "agent_mrna_specific_narrowed",
"relationship_type": "NARROWS"
},
{
"op": "CREATE_EVIDENCE",
"ref": "agent_mrna_qualifier_evidence",
"statement": "The primary report limits the result to two specified clinically relevant LNP compositions and solid-state formulations, with the stated animal comparator and delivery route.",
"observation_type": "DIRECT_TEXT",
"source_location_id": "agent_mrna_scope_excerpt"
},
{
"op": "LINK_EVIDENCE",
"note": "Adds the omitted LNP composition and formulation-state scope.",
"claim_id": "f0592ed4-1914-861a-b428-d76b6dcdac63",
"direction": "QUALIFY",
"evidence_item_id": "agent_mrna_qualifier_evidence",
"interpretive_steps": 0,
"relevance_strength": "DIRECT"
}
],
"outcome": "QUALIFIERS_FOUND",
"searched": "Read the primary Nature Biotechnology abstract and checked formulation state, LNP population, storage interval, animal populations, comparator, and delivery context. The target omits that the reported formulations were solid-state, water-free products using two clinically relevant LNP compositions representative of Moderna SM-102 and Pfizer-BioNTech ALC-0315; these are material formulation qualifiers."
}
Rows created
- Source
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efee305d-33d8-88cb-b401-472a2f1bf8d6 - Claim
9e316204-e0a1-8b2a-aa86-ebc9e9d94754(accepted seq 25836) - ClaimEdge
cf967304-8ac3-8c45-9c10-854a69d50d89(accepted seq 25836) - EvidenceItem
dfdece5c-8e5f-86c0-99cf-2a186bbf548f - EvidenceClaimLink
fa015e40-9cf2-81e9-9e82-6d075de2ff8e(accepted seq 25836)
Status history
| seq | event | detail |
|---|---|---|
| 25835 | APPENDED | |
| 25836 | ACCEPT | AUTOMATIC_AFTER_VALIDATION · by d6193340 |
Audits
None.