Evidence map›Paper›PMID 22051115›Full record

ReviewSeminars in immunology2012

Chronic alloantibody mediated rejection.

R Neal Smith, Robert B Colvin

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in immunology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Transplantology: Challenges for Today.Archivum immunologiae et therapiae experimentalis · 2016
    Review
  11. Review
  12. B Cells, Antibodies, and More.Clinical journal of the American Society of Nephrology : CJASN · 2016
    Review
  13. Lupus-Prone Mice Resist Immune Regulation and Transplant Tolerance Induction.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2016
    Article
  14. ABO-compatible liver allograft antibody-mediated rejection: an update.Current opinion in organ transplantation · 2015
    Review
  15. Graft microvascular disease in solid organ transplantation.Journal of molecular medicine (Berlin, Germany) · 2014
    Review
  16. Article
  17. Lessons and limits of mouse models.Cold Spring Harbor perspectives in medicine · 2013
    Review
  18. Reversing endogenous alloreactive B cell GC responses with anti-CD154 or CTLA-4Ig.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2013
    Article
  19. 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 at 1 institution in 1 country.

R Neal SmithDepartment of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA. rnsmith@partners.org
Robert B Colvin
Massachusetts General Hospital · US

Funding

Tolerance to Composite Islet-Kidney Transplants in Non-Human PrimatesU19AI102405 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI COSIMI, A BENEDICT · 2012 to 2016
$7.7M
NIAID NIH HHS U19 AI102405
6 · The paper itself

Abstract

Alloantibodies clearly cause acute antibody mediated rejection, and all available evidence supports their pathogenic etiology in the development of chronic alloantibody mediated rejection (CAMR). But the slow evolution of this disease, the on-going immunosuppression, the variations in titer of alloantibodies, and variation in antigenic targets all complicate identifying which dynamic factors are most important clinically and pathologically. This review highlights the pathological factors related to the diagnosis of CAMR, the time course and natural history of this disease. What is known about CAMR pathogenesis is discussed including alloantibodies, the role of complement, gene activation, and Fc effector cell function. Therapy, which is problematic for this disease, is also discussed, including on-going and potential therapies and their limitations.

Indexed as

Chronic DiseaseComplement System ProteinsGraft RejectionHumansIsoantibodiesTransplantation, HomologousComplement System ProteinsIsoantibodies

Identifiers

PMID22051115
PMCPMC3728653
OpenAlexW2065695595

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.