MétaCan
Menu
Back to cohort
Record W2571474109 · doi:10.1182/blood.v118.21.42.42

Intravenous Gammaglobulin (IVIg) Therapy Prevents Antibody-Mediated Transfusion Related Acute Lung Injury (TRALI) by Directly Inhibiting Recipient Neutrophil Activation in a Murine Model

2011· article· en· W2571474109 on OpenAlexaff
John W. Semple, Michael Kim, Jing Hou, Young Jin Lee, Arata Tabuchi, Wolfgang M. Kuebler, Alan H. Lazarus

Bibliographic record

VenueBlood · 2011
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicBlood disorders and treatments
Canadian institutionsCanadian Blood ServicesSt. Michael's Hospital
Fundersnot available
KeywordsMedicineTransfusion-related acute lung injuryImmunologyPulmonary edemaAntibodyLungIn vivoEdemaShock (circulatory)PharmacologyInternal medicine

Abstract

fetched live from OpenAlex

Abstract Abstract 42 Transfusion-related acute lung injury (TRALI) is one of the leading causes of transfusion-related fatalities and most TRALI reactions are thought to be caused by donor antibodies. Because intravenous gammaglobulin (IVIg) therapy has been shown to be beneficial in many antibody-mediated disorders, we hypothesized that IVIg would be effective in treating antibody-mediated TRALI. TRALI was induced in CB.17 SCID mice by injection of an anti-murine major histocompatibility complex (MHC) class I antibody (34-1-2s). The mice were treated with doses of IVIg either prophylactically 18 hours before TRALI induction or after the first symptoms of TRALI were observed (within 3 minutes after 34-1-2s injection). Body temperatures, lung edema, mortality and neutrophil activation were assessed. In IVIg non-treated mice, injection of 34-1-2s caused significantly reduced body temperatures indicating systemic shock within 2 minutes post injection. Pulmonary neutrophil accumulation and mortality occurred within 1 hour post 34-1-2s injection and mortality reach 25% by 2 hours post administration. When bone marrow neutrophils were purified after 34-1-2s administration, they produced significantly more reactive oxygen species compared with 34-1-2s non-treated mice. In contrast, if the mice were pre-treated with either 1 or 2 g/kg IVIg 18 hours before 34-1-2s-TRALI induction, they were completely protected from systemic shock, lung edema and mortality. The prophylactic in vivo IVIg treatment also significantly reduced 34-1-2s-induced neutrophil ROS production. IVIg's effect on ROS production appeared to be due to a direct contact mechanism as titrations of IVIg significantly inhibited the ability of neutrophils to produce ROS in vitro. In mice treated with IVIg 2–3 minutes after 34-1-2s-TRALI induction (when symptoms were first observed), there was also significant protection against the lung damage and mortality. In contrast, IVIg treatment was not as effective against acute lung injury induced by acid inhalation. The results suggest that the treatment of antibody-mediated TRALI reactions with IVIg can effectively prevent pulmonary reactions and mortality and it does so by directly interfering with 34-1-2s-induced neutrophil activation. Disclosures: No relevant conflicts of interest to declare.

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)0.000
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 score0.001
Threshold uncertainty score0.004

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0010.000
Research integrity0.0010.002
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 head0.008
GPT teacher head0.235
Teacher spread0.227 · 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
Published2011
Admission routes1
Has abstractyes

Explore more

Same venueBloodSame topicBlood disorders and treatmentsFrench-language works237,207