Evidence map›Paper›PMID 10880058›Full record

ArticleThe Journal of clinical investigation2000

Human allograft acceptance is associated with immune regulation.

A M VanBuskirk, W J Burlingham, E Jankowska-Gan, T Chin, S Kusaka, F Geissler, R P Pelletier, C G Orosz

Abstract read
In one paragraph

Article in The Journal of clinical investigation, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed, 1 pooled it
–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

64 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Review
  4. Regulatory T cells in renal disease.Clinical & translational immunology · 2018
    Review
  5. Review
  6. Review
  7. Measurement of T Cell Alloreactivity Using Imaging Flow Cytometry.Journal of visualized experiments : JoVE · 2017
    Article
  8. Article
  9. Review
  10. Quantification of CD4(+) T Cell Alloreactivity and Its Control by Regulatory T Cells Using Time-Lapse Microscopy and Immune Synapse Detection.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2016
    Article
  11. Review
  12. Article
  13. Article
  14. Immune monitoring post liver transplant.World journal of transplantation · 2014
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article

4 more citing papers are in PubMed but not listed here.

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

8 authors.

A M VanBuskirkDepartment of Surgery, Ohio State University, Columbus, Ohio, USA. vanbuskirk.1@osu.edu
W J Burlingham
E Jankowska-Gan
T Chin
S Kusaka
F Geissler
R P Pelletier
C G Orosz

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI WANCAI YANG · 1985 to 2026
$132.3M
MECHANISMS OF ALLOGRAFT TOLERANCER01HL061966 · NHLBI · OHIO STATE UNIVERSITY · PI OROSZ, CHARLES G · 1999 to 2002
$847k
KIDNEY TRANSPLANTATION &NON-INHERITED MATERNAL ANTIGENSR01AI044077 · NIAID · UNIVERSITY OF WISCONSIN MADISON · PI BURLINGHAM, WILLIAM J · 1999 to 2003
$843k
PRECLINICAL ANALYSIS OF DTH IN TRANSPLANT RECIPIENTSR29AI040909 · NIAID · OHIO STATE UNIVERSITY · PI VANBUSKIRK, ANNE M · 1997 to 2001
$222k
NCI NIH HHS P30 CA016058NCI NIH HHS P30-CA16058NHLBI NIH HHS R01-HL61966NIAID NIH HHS R01 AI044077NIAID NIH HHS R29-AI40909
6 · The paper itself

Abstract

The ultimate goal of transplantation is drug-free allograft acceptance, which is rarely encountered in transplant recipients. Using a novel human-to-mouse "trans vivo" delayed-type hypersensitivity assay, we assessed donor-reactive cell-mediated immune responses in kidney and liver transplant patients, four of whom discontinued all immunosuppression. One of these subjects (J.B.) rejected his graft after 7 years of stable function, while the others (D.S., R.D., M.L.) continue to have excellent graft function 5, 28, and 4 years after the cessation of immunosuppression. PBMCs from J.B. exhibited strong responses to both donor and recall antigens whereas PBMCs from patients D.S., R.D., and M.L. responded strongly to recall, but not donor, antigens. Furthermore, when donor and recall antigens were colocalized, the recall response in these three patients was inhibited. This donor antigen-linked nonresponsiveness was observed in four other patients who are still maintained on immunosuppression. The weakness of donor-reactive DTH responses in these patients is due to donor alloantigen-triggered regulation that relies on either TGF-beta or IL-10. In D.S., regulation is triggered by a single donor HLA Class I antigen, either in membrane-bound or soluble form. This demonstrates that allograft acceptance in humans is associated with an immune regulation pattern, which may be useful in the diagnosis and/or monitoring of transplant patients for allograft acceptance.

Indexed as

AnimalsHistocompatibility TestingHLA-A AntigensHLA-DR AntigensHumansHypersensitivity, DelayedInterleukin-10Kidney TransplantationLiver TransplantationMiceMice, SCIDRabbitsTransforming Growth Factor betaTransplantation, HomologousHLA-A AntigensHLA-DR AntigensInterleukin-10Transforming Growth Factor beta

Identifiers

PMID10880058
PMCPMC314359

What OpenQuestion holds

Textmetadata
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.