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Record W7133063697

The role and mechanisms of double negative regulatory T cells in the prevention of cardiac xenograft rejection

2006· dissertation· W7133063697 on OpenAlexaff
Wenhao Chen

Bibliographic record

VenueTSpace · 2006
Typedissertation
Language
FieldMedicine
TopicXenotransplantation and immune response
Canadian institutionsPublic Health OntarioLibrary and Archives Canada
FundersOffice of Energy Efficiency and Renewable Energy
KeywordsAdoptive cell transferXenotransplantationIn vitroTransplantationAntigenMonoclonal antibodyImmune systemT lymphocyte
DOInot available

Abstract

fetched live from OpenAlex

We have previously identified peripheral alphabetaTCR+CD3 +CD4-CD8- double negative (DN) T cells as a distinct Treg subset. DN Tregs obtained from allograft-tolerant mice can suppress/kill anti-donor T cells in vitro in an antigen specific manner and prolong donor-specific allograft survival in recipient mice following adoptive transfer. In this thesis, I studied the role of DN Tregs in the prevention of organ xenograft rejection. I used a rat-to-mouse cardiac xenotransplantation model, in which CD4+ T cells play a critical role in rejecting xenografts since CD4+ T cell-deficient (CD4-/- ) mice failed to reject rat hearts. I demonstrate that a combination treatment of pretransplant donor lymphocyte infusion (DLI) and a short course of anti-CD4 depleting mAb, but not anti-CD4 mAb alone, induced permanent rat-heart survival in wild type mice. Adoptive transfer CD4+ T cells from DLI/anti-CD4-treated xenograft-accepted mice can induce rejection of rat hearts in CD4-/- mice, indicating the presence of functional anti-donor CD4 + T cells in xenograft-accepted mice. Interestingly, the number of DN Tregs was significantly increased in the secondary lymphoid organs of DLI/anti-CD4-treated xenografted mice when compared to that of anti-CD4-alone treated recipients. DN Tregs isolated from the secondary lymphoid organs of DLI/anti-CD4-, but not anti-CD4-, treated xenografted mice could suppress the in vitro proliferation of anti-donor CD4+ T cells in an antigen-specific manner. In addition, when the number and phenotype of graft-infiltrating cells were compared between anti-CD4- and DLI/anti-CD4-treated groups, I observed a significant increase in both the number and suppressive activity of DN Tregs in the xenografts of DLI/anti-lCD4-treated mice. Thus, DN Tregs may be involved in controlling anti-xenograft CD4+ T cell responses in both secondary lymphoid organs and xenografts. Furthermore, adoptive transfer DN Tregs from xenograft-accepted mice significantly inhibited the in vivo proliferation and cytokine production of transferred naive CD4+ T cells, and prevented transferred CD4+ T cell-mediated rejection of rat cardiac xenografts in CD4-/- mice. These data provide in vivo evidence that DN Tregs are able to control anti-xenograft CD4+ T cell responses. Taken together, I have shown that suppression of anti-donor CD4+ T cells by DN Tregs contributes to the maintenance of xenograft survival.

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 score0.000
Threshold uncertainty score0.002

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.000
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)0.0000.000

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 head0.009
GPT teacher head0.296
Teacher spread0.287 · 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
Published2006
Admission routes1
Has abstractyes

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