Evidence map›Paper›PMID 26705099›Full record

ArticleAmerican journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons2016

Antibody-Mediated Rejection in Sensitized Nonhuman Primates: Modeling Human Biology.

C K Burghuber, J Kwun, E J Page, M Manook, A C Gibby, F V Leopardi, M Song, A B Farris, J J Hong, F Villinger and 3 more

Open 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, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

38 citing papers in PubMed, 51 citations in OpenAlex.

  1. A novel immunoglobulin G- and immunoglobulin cleaving enzyme MG (IceMG), for antibody-mediated rejection.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2026
    Article
  2. Best practices in mouse models of skin transplantation.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Addition of interleukin-6 receptor blockade to carfilzomib-based desensitization in a highly sensitized nonhuman primate model.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2022
    Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Review
  20. 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

13 authors at 5 institutions in 3 countries.

C K BurghuberEmory Transplant Center, Department of Surgery, Emory School of Medicine, Atlanta, GA.
J KwunEmory Transplant Center, Department of Surgery, Emory School of Medicine, Atlanta, GA.
E J PageEmory Transplant Center, Department of Surgery, Emory School of Medicine, Atlanta, GA.
M ManookDuke Transplant Center, Department of Surgery, Duke University, Durham, NC.
A C GibbyEmory Transplant Center, Department of Surgery, Emory School of Medicine, Atlanta, GA.
F V LeopardiEmory Transplant Center, Department of Surgery, Emory School of Medicine, Atlanta, GA.
M SongEmory Transplant Center, Department of Surgery, Emory School of Medicine, Atlanta, GA.
A B FarrisDepartment of Pathology, Emory School of Medicine, Atlanta, GA.
J J HongDepartment of Pathology, Emory School of Medicine, Atlanta, GA.
F VillingerDepartment of Pathology, Emory School of Medicine, Atlanta, GA.
A B AdamsEmory Transplant Center, Department of Surgery, Emory School of Medicine, Atlanta, GA.
N N IwakoshiEmory Transplant Center, Department of Surgery, Emory School of Medicine, Atlanta, GA.
S J KnechtleEmory Transplant Center, Department of Surgery, Emory School of Medicine, Atlanta, GA.
Emory Healthcare · USDuke University · USEmory University · USKorea Research Institute of Bioscience and Biotechnology · KRMedical University of Vienna · AT

Funding

Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
Transplant Tolerance in Non-Human PrimatesU19AI051731 · NIAID · UNIVERSITY OF WESTERN ONTARIO · PI ADAMS, ANDREW B · 2002 to 2022
$54.1M
Nonhuman Primate Reagent ResourceU24AI126683 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Diogo Magnani · 2016 to 2026
$20.1M
Resource for Nonhuman Primate Cell Depleting AntibodiesR24OD010976 · OD · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI ENGELMAN, KATHLEEN, MAGNANI, DIOGO · 2012 to 2019
$4.7M
Austrian Science Fund FWF J 3414NIAID NIH HHS U19 AI051731NIAID NIH HHS U24 AI126683NIH HHS P51 OD011132NIH HHS R24 OD010976
6 · The paper itself

Abstract

We have established a model of sensitization in nonhuman primates and tested two immunosuppressive regimens. Animals underwent fully mismatched skin transplantation, and donor-specific antibody (DSA) response was monitored by flow cross-match. Sensitized animals subsequently underwent kidney transplantation from their skin donor. Immunosuppression included tacrolimus, mycophenolate, and methylprednisolone. Three animals received basiliximab induction; compared with nonsensitized animals, they showed a shorter mean survival time (4.7 ± 3.1 vs. 187 ± 88 days). Six animals were treated with T cell depletion (anti-CD4/CD8 mAbs), which prolonged survival (mean survival time 21.6 ± 19.0 days). All presensitized animals showed antibody-mediated rejection (AMR). In two of three basiliximab-injected animals, cellular rejection (ACR) was prominent. After T cell depletion, three of six monkeys experienced early acute rejection within 8 days with histological evidence of thrombotic microangiopathy and AMR. The remaining three monkeys survived 27-44 days, with mixed AMR and ACR. Most T cell-depleted animals experienced a rebound of DSA that correlated with deteriorating kidney function. We also found an increase in proliferating memory B cells (CD20(+) CD27(+) IgD(-) Ki67(+) ), lymph node follicular helper T cells (ICOS(+) PD-1(hi) CXCR5(+) CD4(+) ), and germinal center (GC) response. Depletion controlled cell-mediated rejection in sensitized nonhuman primates better than basiliximab, yet grafts were rejected with concomitant DSA rise. This model provides an opportunity to test novel desensitization strategies.

Indexed as

Disease Models, AnimalSkin TransplantationAnimalsGraft RejectionHumansImmunosuppressive AgentsIsoantibodiesKidney TransplantationLymphocyte DepletionMacaca mulattaMaleT-Lymphocytes, Helper-InducerImmunosuppressive AgentsIsoantibodies

Identifiers

PMID26705099
PMCPMC4874845
OpenAlexW2221834647

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.