Evidence map›Paper›PMID 29136317›Full record

ArticleAmerican journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons2018

IL-7 receptor heterogeneity as a mechanism for repertoire change during postdepletional homeostatic proliferation and its relation to costimulation blockade-resistant rejection.

He Xu, Victoria A Bendersky, Todd V Brennan, Jaclyn R Espinosa, Allan D Kirk

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00565773 (Use of Belatacept During Post Depletional Repopulation to Facilitate Tolerance in Renal Allograft Recipients), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 30% 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.

NCT00565773 phase2completednot on this map

Use of Belatacept During Post Depletional Repopulation to Facilitate Tolerance in Renal Allograft Recipients

TypeinterventionalSponsorAllan D Kirk, MD, PhDRan2007 to 2017Enrolled40ConditionsOrgan TransplantationArmsBelatacept, Sirolimus, Alemtuzumab
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Age-related effects on thymic output and homeostatic T cell expansion following depletional induction in renal transplant recipients.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2021
    Article
  3. Review
  4. CD69+ resident memory T cells are associated with graft-versus-host disease in intestinal transplantation.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2021
    Article
  5. Functional Characteristics and Phenotypic Plasticity of CD57Journal of immunology (Baltimore, Md. : 1950) · 2021
    Article
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

5 authors at 1 institution in 1 country.

He XuDepartment of Surgery, Duke University Medical Center, Durham, NC, USA.
Victoria A BenderskyDepartment of Surgery, Duke University Medical Center, Durham, NC, USA.
Todd V BrennanDepartment of Surgery, Duke University Medical Center, Durham, NC, USA.
Jaclyn R EspinosaDepartment of Surgery, Duke University Medical Center, Durham, NC, USA.
Allan D KirkDepartment of Surgery, Duke University Medical Center, Durham, NC, USA.
Duke Medical Center · US

Funding

Phase 2 Study of Belatacept, Alemtuzumab, and Sirolimus in Renal TransplantationR01FD003539 · FDA · EMORY UNIVERSITY · PI KIRK, ALLAN D. · 2008 to 2019
$3.8M
T Cell Maturation and the Nexus of Viral- and Allo-ImmunityR01AI097423 · NIAID · EMORY UNIVERSITY · PI KIRK, ALLAN D. · 2012 to 2016
$2.6M
Role of Endogenous Toll-Like Receptor Ligands in Allospecific T Cell ActivationK08AI101263 · NIAID · DUKE UNIVERSITY · PI BRENNAN, TODD VICTOR · 2012 to 2016
$644k
FDA HHS R01 FD003539NIAID NIH HHS K08 AI101263NIAID NIH HHS R01 AI097423
6 · The paper itself

Abstract

Kidney transplant patients treated with belatacept without depletional induction experience higher rates of acute rejection compared to patients treated with conventional immunosuppression. Costimulation blockade-resistant rejection (CoBRR) is associated with terminally differentiated T cells. Alemtuzumab induction and belatacept/sirolimus immunotherapy effectively prevent CoBRR. We hypothesized that cells in late phases of differentiation would be selectively less capable than more naive phenotypes of repopulating postdepletion, providing a potential mechanism by which lymphocyte depletion and repopulation could reduce the risk of CoBRR. Lymphocytes from 20 recipients undergoing alemtuzumab-induced depletion and belatacept/sirolimus immunosuppression were studied longitudinally for markers of maturation (CCR7, CD45RA, CD57, PD1), recent thymic emigration (CD31), and the IL-7 receptor-α (IL-7Rα). Serum was analyzed for IL-7. Alemtuzumab induction produced profound lymphopenia followed by repopulation, during which naive IL-7Rα

Indexed as

Cell ProliferationKidney TransplantationLymphocyte DepletionAbataceptCD57 AntigensGraft RejectionGraft SurvivalHumansImmunologic MemoryImmunosuppressive AgentsInterleukin-7PrognosisReceptors, Interleukin-7Risk FactorsAbataceptCD57 AntigensImmunosuppressive AgentsInterleukin-7interleukin-7 receptor, alpha chainReceptors, Interleukin-7basic (laboratory) research/scienceclinical research/practicecytokines/cytokine receptorsimmunobiologyimmunosuppressant - fusion proteins and monoclonal antibodies: belataceptimmunosuppressant - mechanistic target of rapamycin: sirolimusimmunosuppression/immune modulationimmunosuppressive regimens - inductionkidney transplantation/nephrologylymphocyte biology: differentiation/maturation

Identifiers

PMID29136317
PMCPMC6035390
OpenAlexW2770109483

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.