Evidence map›Paper›PMID 27481849›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2016

Enhanced Requirement for TNFR2 in Graft Rejection Mediated by Low-Affinity Memory CD8+ T Cells during Heterologous Immunity.

Scott M Krummey, Ching-Wen Chen, Sara A Guasch, Danya Liu, Maylene Wagener, Christian P Larsen, Mandy L Ford

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 27% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Scott M KrummeyEmory Transplant Center, Emory University, Atlanta, GA 30322.
Ching-Wen ChenEmory Transplant Center, Emory University, Atlanta, GA 30322.
Sara A GuaschEmory Transplant Center, Emory University, Atlanta, GA 30322.ORCID 0000-0002-5275-1821
Danya LiuEmory Transplant Center, Emory University, Atlanta, GA 30322.ORCID 0000-0001-6103-6486
Maylene WagenerEmory Transplant Center, Emory University, Atlanta, GA 30322.
Christian P LarsenEmory Transplant Center, Emory University, Atlanta, GA 30322.
Mandy L FordEmory Transplant Center, Emory University, Atlanta, GA 30322 mandy.ford@emory.edu.
Emory University · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM008169 · NIGMS · EMORY UNIVERSITY · PI GROSS, ROBERT E · 1987 to 2021
$20.3M
TRAINING IN IMMUNOLOGY AND MOLECULAR PATHOGENESIST32AI007610 · NIAID · EMORY UNIVERSITY · PI EVAVOLD, BRIAN D · 2000 to 2014
$4.4M
Activation, Apathy, Anergy and Apoptosis in TransplantationR37AI040519 · NIAID · EMORY UNIVERSITY · PI LARSEN, CHRISTIAN P. · 2007 to 2016
$4.1M
Determinants of T Cell Fate in Transplantation ToleranceR01AI073707 · NIAID · EMORY UNIVERSITY · PI FORD, MANDY L · 2008 to 2021
$4.0M
Advanced Research Training in Transplantation ScienceT32AI070081 · NIAID · EMORY UNIVERSITY · PI Mandy L Ford · 2006 to 2026
$3.1M
Costimulatory and Coinhibitory Receptor Control of Alloreactive T Cell ResponsesR01AI104699 · NIAID · EMORY UNIVERSITY · PI FORD, MANDY L · 2013 to 2017
$2.1M
Novel Costimulation Blockers in Islet TransplantationF30DK098928 · NIDDK · EMORY UNIVERSITY · PI KRUMMEY, SCOTT M · 2013 to 2014
$94k
NIAID NIH HHS R01 AI073707NIAID NIH HHS R01 AI104699NIAID NIH HHS R37 AI040519NIAID NIH HHS T32 AI007610NIAID NIH HHS T32 AI070081NIDDK NIH HHS F30 DK098928NIGMS NIH HHS T32 GM008169
6 · The paper itself

Abstract

The affinity of a TCR binding to peptide:MHC profoundly impacts the phenotype and function of effector and memory cell differentiation. Little is known about the effect of low-affinity priming on memory cell generation and function, which is particularly important in heterologous immunity, when microbe-specific T cells cross-react with allogeneic Ag and mediate graft rejection. We found that low-affinity-primed memory CD8(+) T cells produced high levels of TNF ex vivo in response to heterologous rechallenge compared with high-affinity-primed memory T cells. Low-affinity secondary effectors significantly upregulated TNFR2 on the cell surface and contained a higher frequency of TNFR2(hi) proliferating cells. Low-affinity-primed secondary effectors concurrently downregulated TNF production. Importantly, blockade of TNFR2 attenuated graft rejection in low- but not high-affinity-primed animals. These data establish a functional connection between TNF signaling and TCR-priming affinity and have implications for the immunomodulation of pathogenic T cell responses during transplantation.

Indexed as

Immunity, HeterologousImmunologic MemoryAnimalsAntibody AffinityCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell DifferentiationGraft RejectionMiceMice, Inbred C57BLReceptors, Tumor Necrosis Factor, Type IISkin TransplantationTumor Necrosis Factor-alphaReceptors, Tumor Necrosis Factor, Type IITumor Necrosis Factor-alpha

Identifiers

PMID27481849
PMCPMC4992585
OpenAlexW2494514697

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.