Evidence map›Paper›PMID 40662367›Full record

ArticleThe Journal of clinical investigation2025

Chemokine gradients spare graft endothelium from CD8+ T cell-mediated injury during allograft rejection.

Scott M Krummey, Jonathan S Bromberg

Abstract read
In one paragraph

Article in The Journal of clinical investigation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

2 authors.

Scott M KrummeyDepartment of Pathology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Jonathan S BrombergUniversity of Maryland School of Medicine, Departments of Surgery and Microbiology and Immunology, Center for Vascular and Inflammatory Diseases, Baltimore, Maryland, USA.

Funding

Lymph Node Structure and Function in Tolerance: Role of LamininsR01AI114496 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI BROMBERG, JONATHAN S · 2015 to 2024
$4.2M
Role of the CD43 Receptor on Effector CD8+ T Cells During Acute Allograft RejectionR56AI179856 · NIAID · JOHNS HOPKINS UNIVERSITY · PI KRUMMEY, SCOTT M · 2024 to 2024
$328k
NIAID NIH HHS R01 AI114496NIAID NIH HHS R56 AI179856
6 · The paper itself

Abstract

T cell-mediated rejection (TCMR) develops after alloantigen-primed T cells migrate into an allograft to cause tissue damage. In contrast to antibody-mediated rejection, which creates lesions in the graft vasculature, injury to the graft vasculature is often limited during TCMR. In this issue of the JCI, Barba et al. investigated the mechanism by which the endothelium is spared from harm caused by graft-infiltrating CD8+ T cells. Endothelial cell protection was due to cell-extrinsic chemokine variations in the environment, rather than cell-intrinsic differences between endothelial and interstitial cells. The CXCL12 gradient in particular facilitated CD8+ T cell movement through the endothelial layer into the graft parenchyma. These findings suggest that targeting the CXCL12 pathway may prevent or alleviate TCMR.

Indexed as

CD8-Positive T-LymphocytesChemokine CXCL12Endothelium, VascularGraft RejectionAllograftsAnimalsEndothelial CellsHumansMiceChemokine CXCL12Cxcl12 protein, mouse

Identifiers

PMID40662367
PMCPMC12259266

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Registered trials

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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.