Evidence map›Paper›PMID 19426498›Full record

ArticleBMC immunology2009

Antibody-mediated immunity to the obligate intracellular bacterial pathogen Coxiella burnetii is Fc receptor- and complement-independent.

Jeffrey G Shannon, Diane C Cockrell, Kazue Takahashi, Gregory L Stahl, Robert A Heinzen

Open access · goldAbstract read
In one paragraph

Article in BMC immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

25 citing papers in PubMed, 40 citations in OpenAlex.

  1. Opsonization Improves Dual Proteomic Analysis ofJournal of proteome research · 2026
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  16. Functions of Antibodies.Microbiology spectrum · 2014
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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

5 authors at 4 institutions in 1 country.

Jeffrey G ShannonCoxiella Pathogenesis Section, Laboratory of Intracellular Parasites, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana, USA. jshannon@niaid.nih.gov
Diane C Cockrell
Kazue Takahashi
Gregory L Stahl
Robert A Heinzen
National Institutes of Health · USBrigham and Women's Hospital · USHarvard University · USNational Institute of Allergy and Infectious Diseases · US

Funding

Specialized Center for Oral Inflammation and ResolutionP50DE016191 · NIDCR · BRIGHAM AND WOMEN'S HOSPITAL · PI SERHAN, CHARLES NICHOLAS · 2004 to 2010
$13.6M
Cellular and Developmental Biology of Coxiella burnetiiZIAAI000931 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI HEINZEN, ROBERT A · 2009 to 2023
$11.8M
The Role of Complement in Protection against SLEP01AI052343 · NIAID · IMMUNE DISEASE INSTITUTE, INC. · PI CARROLL, MICHAEL CRAIG · 2002 to 2006
$7.6M
MECHANISMS OF COMPLEMENT INDUCED MYOCARDIAL ISCHEMIAR01HL052886 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI STAHL, GREGORY L · 1999 to 2007
$3.5M
Microglia, Complement, and PainR01DE017821 · NIDCR · MASSACHUSETTS GENERAL HOSPITAL · PI WOOLF, CLIFFORD J · 2006 to 2010
$2.4M
MECHANISMS OF COMPLEMENT INDUCED MYOCARDIAL ISCHEMIAR29HL052886 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI STAHL, GREGORY L · 1995 to 1998
–
Intramural NIH HHSNHLBI NIH HHS HL52886NHLBI NIH HHS HL56068NHLBI NIH HHS R01 HL052886NIAID NIH HHS AI052343NIAID NIH HHS P01 AI052343NIDCR NIH HHS DE016191NIDCR NIH HHS DE017821NIDCR NIH HHS P50 DE016191NIDCR NIH HHS R01 DE017821
6 · The paper itself

Abstract

backgroundThe obligate intracellular bacterial pathogen Coxiella burnetii causes the zoonosis Q fever. The intracellular niche of C. burnetii has led to the assumption that cell-mediated immunity is the most important immune component for protection against this pathogen. However, passive immunization with immune serum can protect naïve animals from challenge with virulent C. burnetii, indicating a role for antibody (Ab) in protection. The mechanism of this Ab-mediated protection is unknown. Therefore, we conducted a study to determine whether Fc receptors (FcR) or complement contribute to Ab-mediated immunity (AMI) to C. burnetii.

resultsVirulent C. burnetii infects and replicates within human dendritic cells (DC) without inducing their maturation or activation. We investigated the effects of Ab opsonized C. burnetii on human monocyte-derived and murine bone marrow-derived DC. Infection of DC with Ab-opsonized C. burnetii resulted in increased expression of maturation markers and inflammatory cytokine production. Bacteria that had been incubated with naïve serum had minimal effect on DC, similar to virulent C. burnetii alone. The effect of Ab opsonized C. burnetii on DC was FcR dependent as evidenced by a reduced response of DC from FcR knockout (FcR k/o) compared to C57Bl/6 (B6) mice. To address the potential role of FcR in Ab-mediated protection in vivo, we compared the response of passively immunized FcR k/o mice to the B6 controls. Interestingly, we found that FcR are not essential for AMI to C. burnetii in vivo. We subsequently examined the role of complement in AMI by passively immunizing and challenging several different strains of complement-deficient mice and found that AMI to C. burnetii is also complement-independent.

conclusionDespite our data showing FcR-dependent stimulation of DC in vitro, Ab-mediated immunity to C. burnetii in vivo is FcR-independent. We also found that passive immunity to this pathogen is independent of complement.

Indexed as

AnimalsAntibody-Dependent Cell CytotoxicityAntigen-Antibody ComplexAntigens, BacterialCell DifferentiationComplement ActivationComplement System ProteinsCoxiella burnetiiDendritic CellsImmunization, PassiveImmunoglobulin GMiceMice, Inbred C57BLMice, KnockoutQ FeverReceptors, FcAntigen-Antibody ComplexAntigens, BacterialComplement System ProteinsImmunoglobulin GReceptors, Fc

Identifiers

PMID19426498
PMCPMC2689861
OpenAlexW2111248948

What OpenQuestion holds

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Registered trials

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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.