Evidence map›Paper›PMID 28654684›Full record

Observational studyPloS one2017

Intravenous immunoglobulin therapy in kidney transplant recipients with de novo DSA: Results of an observational study.

Marie Matignon, Caroline Pilon, Morgane Commereuc, Cynthia Grondin, Claire Leibler, Tomek Kofman, Vincent Audard, José Cohen, Florence Canoui-Poitrine, Philippe Grimbert

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

5 citing papers in PubMed, 14 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. 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

10 authors at 3 institutions in 1 country.

Marie MatignonAP-HP, Henri Mondor Hospital, Nephrology and Transplantation Department and CIC Biothérapies 504, Créteil, France.
Caroline PilonINSERM U955, Team 21, Créteil, France and Paris Est University (UPEC), Créteil, France.
Morgane CommereucAP-HP, Henri Mondor Hospital, Nephrology and Transplantation Department, Créteil, France.
Cynthia GrondinAP-HP, Henri Mondor Hospital, CIC Biothérapies 504, Créteil France.
Claire LeiblerINSERM U955, Team 21, Créteil, France and Paris Est University (UPEC), Créteil, France.
Tomek KofmanAP-HP, Henri Mondor Hospital, Nephrology and Transplantation Department, Créteil, France.
Vincent AudardINSERM U955, Team 21, Créteil, France and Paris Est University (UPEC), Créteil, France.
José CohenINSERM U955, Team 21, Créteil, France and Paris Est University (UPEC), Créteil, France.
Florence Canoui-PoitrineAP-HP, Henri-Mondor Hospital, Public Health Department, Creteil, France.
Philippe GrimbertAP-HP, Henri Mondor Hospital, Nephrology and Transplantation Department and CIC Biothérapies 504, Créteil, France.ORCID http://orcid.org/0000-0002-8235-2864
Inserm · FRAssistance Publique – Hôpitaux de Paris · FRUniversité Paris-Est Créteil · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundApproximately 25% of kidney transplant recipients develop de novo anti-HLA donor-specific antibodies (dnDSA) leading to acute antibody-mediated rejection (ABMR) in 30% of patients. Preemptive therapeutic strategies are not available.

methodsWe conducted a prospective observational study including 11 kidney transplant recipients. Inclusion criteria were dnDSA occurring within the first year after transplant and normal allograft biopsy. All patients were treated with high-dose IVIG (2 g/kg 0, 1 and 2 months post-dnDSA). The primary efficacy outcome was incidence of clinical and subclinical acute ABMR within 12 months after dnDSA detection as compared to a historical control group (IVIG-).

resultsAcute ABMR occurred in 2 or 11 patients in the IVIG+ group and in 1 of 9 patients in the IVIG- group. IVIG treatment did not affect either class I or class II DSA, as observed at the end of the follow-up. IVIG treatment significantly decreased FcγRIIA mRNA expression in circulating leukocytes, but did not affect the expression of any other markers of B cell activation.

conclusionsIn this first pilot study including kidney allograft recipients with early dnDSA, preemptive treatment with high-dose IVIG alone did not prevent acute ABMR and had minimal effects on DSA outcome and B cell phenotype.

Indexed as

Kidney TransplantationAdultAgedFemaleGraft RejectionGraft SurvivalHLA AntigensHumansImmunoglobulins, IntravenousIsoantibodiesMaleMiddle AgedPilot ProjectsProspective StudiesTransplant RecipientsTreatment OutcomeHLA AntigensImmunoglobulins, IntravenousIsoantibodies

Identifiers

PMID28654684
PMCPMC5487035
OpenAlexW2731486760

What OpenQuestion holds

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LicenceCC BY
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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.