Evidence map›Paper›PMID 28652397›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2017

B Cells Produce Type 1 IFNs in Response to the TLR9 Agonist CpG-A Conjugated to Cationic Lipids.

Munir Akkaya, Billur Akkaya, Pietro Miozzo, Mukul Rawat, Mirna Pena, Patrick W Sheehan, Ann S Kim, Olena Kamenyeva, Juraj Kabat, Silvia Bolland and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

23 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
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  7. Targeting inflammation as cancer therapy.Journal of hematology & oncology · 2024
    Review
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  14. Changes in Transcript, Metabolite, and Antibody Reactivity During the Early Protective Immune Response in Humans to Mycobacterium tuberculosis Infection.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2020
    Article
  15. Review
  16. Review
  17. Review
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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

12 authors at 2 institutions in 2 countries.

Munir AkkayaLaboratory of Immunogenetics, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD 20852; spierce@nih.gov munir.akkaya@nih.gov.ORCID 0000-0002-9949-9424
Billur AkkayaLaboratory of Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892.ORCID 0000-0002-6808-3776
Pietro MiozzoLaboratory of Immunogenetics, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD 20852.ORCID 0000-0003-3486-4061
Mukul RawatIndian Institute of Science Education and Research, Pune 411 008, India; and.
Mirna PenaLaboratory of Immunogenetics, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD 20852.
Patrick W SheehanLaboratory of Immunogenetics, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD 20852.
Ann S KimLaboratory of Immunogenetics, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD 20852.ORCID 0000-0001-6709-4089
Olena KamenyevaBiological Imaging Facility, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892.
Juraj KabatBiological Imaging Facility, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892.
Silvia BollandLaboratory of Immunogenetics, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD 20852.
Akanksha ChaturvediIndian Institute of Science Education and Research, Pune 411 008, India; and.ORCID 0000-0002-4010-5646
Susan K PierceLaboratory of Immunogenetics, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD 20852; spierce@nih.gov munir.akkaya@nih.gov.ORCID 0000-0001-7261-3437
National Institutes of Health · USIndian Institute of Science Education and Research Pune · IN

Funding

Infectious Diseases Research Technologies Core - BethesdaZICAI001051 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI CHERRY, JAMES · 2009 to 2025
$226.1M
Genetic Modifiers Of Autoimmune Disease In FcgammaRIIB Mutant MiceZIAAI000912 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI BOLLAND, SILVIA · 2009 to 2025
$27.0M
Intracellular Trafficking and Signaling Of The B-cell Antigen ReceptorZIAAI000899 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI PIERCE, SUSAN · 2009 to 2018
$5.5M
The Mechanism of Co-Receptor Regulation of B-cell ActivationZIAAI000975 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI PIERCE, SUSAN · 2009 to 2018
$4.5M
Intracellular Trafficking Of The B-cell Antigen ReceptorZ01AI000899 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI PIERCE, SUSAN · 2001 to 2008
$625k
Intramural NIH HHS Z01 AI000899
6 · The paper itself

Abstract

B cells express the innate receptor, TLR9, which signals in response to unmethylated CpG sequences in microbial DNA. Of the two major classes of CpG-containing oligonucleotides, CpG-A appears restricted to inducing type 1 IFN in innate immune cells and CpG-B to activating B cells to proliferate and produce Abs and inflammatory cytokines. Although CpGs are candidates for adjuvants to boost innate and adaptive immunity, our understanding of the effect of CpG-A and CpG-B on B cell responses is incomplete. In this study we show that both CpG-B and CpG-A activated B cells in vitro to proliferate, secrete Abs and IL-6, and that neither CpG-B nor CpG-A alone induced type 1 IFN production. However, when incorporated into the cationic lipid, DOTAP, CpG-A, but not CpG-B, induced a type 1 IFN response in B cells in vitro and in vivo. We provide evidence that differences in the function of CpG-A and CpG-B may be related to their intracellular trafficking in B cells. These findings fill an important gap in our understanding of the B cell response to CpGs, with implications for the use of CpG-A and CpG-B as immunomodulators.

Indexed as

AnimalsAntibody FormationB-LymphocytesCationsCytokinesImmunity, InnateImmunologic FactorsInterferon Type IInterleukin-6LipidsLymphocyte ActivationMiceOligodeoxyribonucleotidesToll-Like Receptor 9CationsCpG-A 2336CpG-B 2006CPG-oligonucleotideCytokinesImmunologic FactorsInterferon Type IInterleukin-6interleukin-6, mouseLipidsOligodeoxyribonucleotidesToll-Like Receptor 9

Identifiers

PMID28652397
PMCPMC5531204
OpenAlexW2706644550

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.