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Record W4408996090 · doi:10.3889/seejim.2025.6109

Antigen-specific peripheral immune cell dynamics predicting clinical responses to checkpoint blockade in melanoma

2025· article· en· W4408996090 on OpenAlexaff
Graham Pawelec

Bibliographic record

VenueSouth East European Journal of Immunology · 2025
Typearticle
Languageen
FieldMedicine
TopicMonoclonal and Polyclonal Antibodies Research
Canadian institutionsHealth Sciences North
Fundersnot available
KeywordsBlockadeImmune checkpointPeripheralMelanomaImmune systemMedicineImmunologyAntigenCancer researchImmunotherapyInternal medicineReceptor

Abstract

fetched live from OpenAlex

Many years ago, we hypothesized that melanoma patients possessing T cells reacting to cancer antigens would do better than those who did not. To test this, we cultured PBMC from conventionally-treated metastatic melanoma patients with short (6 month) vs. long (18 month) survival with mixtures of peptides representing the shared cancer antigens NY-ESO-1, Melan-A, MAGE-A3 and survivin. After 12 days, cultures were restimulated with the same antigens and 24 h later intracellular cytokines measured by flow cytometry. The results were consistent with there being a clinical benefit of possessing T cells reactive to NY-ESO-1 and Melan-A but not MAGE-A3 or survivin, and patients possessing T cells reactive to both NY-ESO-1 and Melan-A did better than those with T cells responding to either alone. A dissection of the nature of the responding cells indicated that the majority of T cells responding to NY-ESO-1 was CD4+ whereas the majority responding to Melan-A was CD8+. Responding cells producing predominantly proinflammatory cytokines (IFN, TNF) were associated with clinical benefit, whereas IL 4 production was associated with poorer survival. Following these results, recent studies have focussed on whether similar findings apply to stage IV melanoma patients treated with anti-PD-1 antibodies, or a combination of anti-PD-1 and anti-CTLA-4 antibodies. Patients´ PBMCs were tested before the start of checkpoint blockade (baseline, BL) and at a mean of 44 days during ICB (follow-up, FU). In the discovery cohort from 3 clinical centers (n=92) and a validation cohort (n=49), it was confirmed that the presence of NY-ESO-1 and Melan-A-reactive T cells at BL before ICB conferred clinical benefit, both in terms of PFS and OS. Intriguingly, it was further shown that a decrease of these reactive cells at day 44 FU was associated with better survival than either their retention in the blood or their de novo appearance. This was interpreted to suggest sequestration of the reactive cells in the tumour, for which some limited evidence has accrued. By combining such analyses with other blood biomarkers (of which primarily BL and FU lactate dehydrogenase and myeloid-derived suppressor cell dynamics, along with extraordinarily high titers of IgG specific for human herpesvirus 5 (CMV) were associated with clinical outcome), we may approach more closely to the aim of providing robust individualized immune monitoring methods informative for individual patient outcomes.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.001
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.001
Threshold uncertainty score0.005

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.001
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0010.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.032
GPT teacher head0.317
Teacher spread0.285 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations1
Published2025
Admission routes1
Has abstractyes

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