Evidence map›Paper›PMID 20405180›Full record

ReviewJournal of clinical immunology2010

Cell death modulation by intravenous immunoglobulin.

Stephan von Gunten, Hans-Uwe Simon

Abstract readReview
PubMed Publisher
In one paragraph

Review in Journal of clinical immunology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.0field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Multifarious roles of sialic acids in immunity.Annals of the New York Academy of Sciences · 2012
    Review
  11. 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

2 authors at 1 institution in 1 country.

Stephan von GuntenInstitute of Pharmacology, University of Bern, Friedbühlstrasse 49, Bern, Switzerland.
Hans-Uwe Simon
University of Bern · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The induction of cell death in immune cells by naturally occurring antibodies specific for death receptors may present an important antiinflammatory mechanism of intravenous immunoglobulin (IVIG). Conversely, the protection of tissue cells from death receptor-mediated apoptosis by blocking antibodies is thought to contribute to the beneficial effects of IVIG in certain inflammatory disorders such as toxic epidermal necrolysis, also known as Lyell's syndrome. In this review, we focus on recent insights into the role of functional antibodies against Fas, sialic acid-binding immunoglobulin-like lectin (Siglec)-8, and Siglec-9 receptors in IVIG-mediated cell survival or death effects. In addition, we examine a variety of factors in inflammatory disease that may interplay with these cellular events and influence the therapeutic efficacy or potency of IVIG. These involve activation status of the target cell, cytokine microenvironment, pathogenesis and stage of disease, individual genetic determinants, species characteristics, and batch-to-batch variations of IVIG preparations.

Indexed as

Antibody SpecificityAntigens, CDAntigens, Differentiation, B-LymphocyteApoptosisAutoantibodiesAutoantigensEosinophilsfas ReceptorHumansImmunoglobulins, IntravenousInflammationIsoantibodiesLectinsModels, ImmunologicalNeutrophilsSialic Acid Binding Immunoglobulin-like LectinsAntigens, CDAntigens, Differentiation, B-LymphocyteAutoantibodiesAutoantigensFAS protein, humanfas ReceptorImmunoglobulins, IntravenousIsoantibodiesLectinsSialic Acid Binding Immunoglobulin-like LectinsSIGLEC8 protein, humanSIGLEC9 protein, human

Identifiers

PMID20405180
OpenAlexW2059456135

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.