Evidence map›Paper›PMID 19864604›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2009

Complement activation by CpG in a human whole blood loop system: mechanisms and immunomodulatory effects.

Sara M Mangsbo, Javier Sanchez, Kerstin Anger, John D Lambris, Kristina Nilsson Ekdahl, Angelica S Loskog, Bo Nilsson, Thomas H Tötterman

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

16 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Strategies to improve safety profile of AAV vectors.Frontiers in molecular medicine · 2022
    Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
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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

8 authors at 3 institutions in 2 countries.

Sara M MangsboDepartment of Oncology, Radiology and Clinical Immunology, Division of Clinical Immunology, Uppsala University, Uppsala, Sweden. Sara.mangsbo@klinimm.uu.se
Javier Sanchez
Kerstin Anger
John D Lambris
Kristina Nilsson Ekdahl
Angelica S Loskog
Bo Nilsson
Thomas H Tötterman
Uppsala University · SEUppsala University Hospital · SEUniversity of Pennsylvania · US

Funding

Role of complement in kidney disorders: from hemodialysis to transportationP01AI068730 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI LAMBRIS, JOHN D · 2007 to 2018
$16.0M
STRUCTURAL-FUNCTIONAL ANALYSIS OF COMPSTATINR01GM062134 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI LAMBRIS, JOHN D · 2001 to 2010
$2.5M
NIAID NIH HHS AI-068730NIAID NIH HHS P01 AI068730NIGMS NIH HHS GM-62134NIGMS NIH HHS R01 GM062134
6 · The paper itself

Abstract

Phosphorothioate oligodeoxynucleotides can activate complement, and experimental murine studies have revealed differential effects upon simultaneous TLR stimulation and complement activation compared with either event alone. We set out to investigate the immune stimulatory effects of CpG 2006 in fresh non-anticoagulated human blood with or without presence of active complement. We also sought to elucidate the mechanism behind complement activation upon stimulation with phosphorothioate CpG 2006. In a human blood loop system, both backbone and sequence-specific effects by CpG were counteracted by selective inhibition of C3. Furthermore, DNA backbone-mediated CD40 and CD83 expression on monocytes and sequence-specific IL-6 and TNF production were reduced by complement inhibition. CpG-induced complement activation occurred via either the classical or the alternative pathway and deposits of both IgM and properdin, two activators of complement, were detected on CpG after incubation with EDTA plasma. Quartz crystal microbalance with dissipation monitoring demonstrated alternative pathway convertase build-up onto CpG as a likely pathway to initiate and sustain complement activation. Specific inhibition of C3 suppressed CpG 2006 uptake into monocytes indicating that C3 fragments are involved in CpG internalization. The interplay between complement and TLR9 signaling demonstrated herein warrants further investigation.

Indexed as

Adjuvants, ImmunologicAntigens, CDCD40 AntigensCD83 AntigenComplement ActivationComplement Pathway, AlternativeComplement System ProteinsCytokinesHumansImmunoglobulin MImmunoglobulinsInterleukin-6Membrane GlycoproteinsMonocytesOligodeoxyribonucleotidesPeptides, CyclicAdjuvants, ImmunologicAntigens, CDCD40 AntigensCD83 AntigenComplement System ProteinscompstatinCPG-oligonucleotideCytokinesIL6 protein, humanImmunoglobulin MImmunoglobulinsInterleukin-6Membrane GlycoproteinsOligodeoxyribonucleotidesPeptides, CyclicPhosphorothioate OligonucleotidesProperdinTumor Necrosis Factor-alpha

Identifiers

PMID19864604
PMCPMC2857538
OpenAlexW1808677409

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.