Evidence map›Paper›PMID 16760575›Full record

ReviewImmunologic research2006

The role of complement in danger sensing and transmission.

Jörg Köhl

Abstract readReview
PubMed Publisher
In one paragraph

Review in Immunologic research, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
14.1field-weighted citation impact, top 1% 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

73 citing papers in PubMed, 168 citations in OpenAlex.

  1. Article
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  10. The Role of Inflammation in Cholestatic Liver Injury.Journal of inflammation research · 2023
    Review
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  13. Article
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13 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

1 author at 1 institution in 1 country.

Jörg KöhlDivision of Molecular Immunology, Cincinnati Children's Hospital Medical Center and University of Cincinnati College of Medicine, Cincinnati, Ohio 45229, USA. Joerg.Koehl@chmcc.org
Cincinnati Children's Hospital Medical Center · US

Funding

Complement in Allergic Asthma: The role of C3a and C5aR01AI057839 · NIAID · CINCINNATI CHILDRENS HOSP MED CTR · PI KOEHL, JOERG · 2004 to 2008
$1.8M
Molecular regulation of immune complex diseaseR01AI059305 · NIAID · CINCINNATI CHILDRENS HOSP MED CTR · PI KOEHL, JOERG · 2005 to 2009
$1.7M
NIAID NIH HHS R01-AI057839NIAID NIH HHS R01-AI059305
6 · The paper itself

Abstract

Self-non-self discrimination has long been considered the main function of the immune system. Increasing evidence supports the view of the immune system as a network of complex danger sensors and transmitters in which self-non-self discrimination is only one facet. To meet the challenge of danger sensing, the immune system carries a large stock of germline-encoded, highly conserved molecules that can recognize microbial as well as modified host structures. Among those are the Toll-like receptors (TLR), which comprise a dozen membrane-bound pattern-recognition receptors that directly link danger recognition to danger transmission through activation of several distinct cellular signaling pathways. Here, I discuss the function and biology of a complex, evolutionary ancient system, the complement system, which has long been considered critical to host defense. In contrast to TLRs, the complement system senses danger by a panel of soluble molecules that can directly bind to specific complement receptors and/or initiate a complex cascade of proteolytic events that lead to the generation of soluble complement fragments able to bind to another, distinct set of specific complement receptors. As I will outline in this review, complement- mediated danger sensing and the complex transition of this information into distinct cellular activation profiles is critical for tissue homeostasis under steady-state conditions and in response to infection and cell injury. Furthermore, I will discuss recent findings that support a concept of intense cross-talk between the complement system and TLRs, which defines the quality and the magnitude of immune responses in vivo.

Indexed as

Immunity, InnateAnimalsAntigen-Presenting CellsComplement ActivationComplement System ProteinsDendritic CellsHumansLungReceptors, ComplementSignal TransductionToll-Like ReceptorsComplement System ProteinsReceptors, ComplementToll-Like Receptors

Identifiers

PMID16760575
OpenAlexW2136670693

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.