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Record W7115822840

ALLERGEN SPECIFIC B CELLS IN MURINE MODELS

2025· dissertation· en· W7115822840 on OpenAlexfundno aff

Bibliographic record

VenueMacSphere (McMaster University) · 2025
Typedissertation
Languageen
FieldMedicine
TopicAllergic Rhinitis and Sensitization
Canadian institutionsnot available
FundersMcMaster University
KeywordsEpitopeImmunotherapyImmunoglobulin ESplenocyteAntigenAllergenAllergyAntibodyImmune system
DOInot available

Abstract

fetched live from OpenAlex

The prevalence of allergic disease is increasing, with 10-20% of adults globally classified as allergic. Domestic cats are a common source of allergic sensitization, with over 90% of cat allergic individuals being immunoglobulin (Ig) E sensitized to the Felis domesticus (Fel d) 1 protein. During an allergic reaction, affected individuals can experience a wide range of symptoms some of which are life-threatening. Current treatments for cat allergies fail to address the underlying causes of the disease. Peptide immunotherapy using T cell epitopes has demonstrated a strong safety profile and resulted in the development of long-lasting clinical tolerance in studies involving allergic human subjects. However, stability issues, varying responses and manufacturing cost were downsides to the therapy. mRNA peptide immunotherapy vaccines, which encoded the T cell epitopes were a proposed solution. This project aimed to produce and validate Fel d 1 B cell tetramers and to evaluate B cell responses in both naïve and sensitized mice immunized with two prototype vaccines (VXL01, VXL02). Fel d 1 B cell tetramers were produced, tested to ensure specificity and optimized for use in flow cytometry. Splenocytes from mice immunized with vaccine only, immunized with vaccine and given whole-allergen exposure, or allergically sensitized with Fel d 1 and immunized with vaccine were stained and analyzed. Fel d 1 specific B cells were not detected in the vaccine immunized only groups. Neither prototype peptide immunotherapy mRNA vaccine reduced allergic responses in Fel d 1 sensitized mice. There were no statistically significant changes in BAL cellularity, serum IgG and IgE when compared to control at study-endpoint. Fel d 1 sensitized mice immunized with VXL02 had a significantly higher percentage of Fel d 1 tetramer+ B cells than the vehicle alone group, suggesting the vaccine may be capable of activating an established memory B cell pool. In conclusion, performing tetramer analysis on splenocyte populations was both sensitive and antigen-specific. Immunization with prototype vaccines alone did not activate a naïve Fel d 1 specific B cell response but appeared to expand Fel d 1 specific memory B cells. Fel d 1 specific B cells could be detected in mice sensitized to Fel d 1 prior to immunization with the mRNA vaccines with no changes in markers of allergic disease between vaccinated and control groups, indicating the vaccines were not effective at reducing the Th2 allergic disease phenotype.

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)0.002
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: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.008
Threshold uncertainty score0.026

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0020.001
Meta-epidemiology (narrow)0.0020.001
Meta-epidemiology (broad)0.0010.001
Bibliometrics0.0030.001
Science and technology studies0.0010.001
Scholarly communication0.0010.001
Open science0.0010.001
Research integrity0.0030.006
Insufficient payload (model declined to judge)0.0080.004

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 head0.019
GPT teacher head0.210
Teacher spread0.192 · 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 designBench or experimental
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

Citations0
Published2025
Admission routes1
Has abstractyes

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