Evidence map›Paper›PMID 31897428›Full record

Trial reportScience advances2019

Blocking FcRn in humans reduces circulating IgG levels and inhibits IgG immune complex-mediated immune responses.

L J Blumberg, J E Humphries, S D Jones, L B Pearce, R Holgate, A Hearn, J Cheung, A Mahmood, B Del Tito, J S Graydon and 13 more

Open access · goldAbstract readClinical Trial, Phase IRandomized Controlled Trial
In one paragraph

Trial report in Science advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
8.9field-weighted citation impact, top 2% 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

75 citing papers in PubMed, 120 citations in OpenAlex.

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  7. Targeting FcRn for immunomodulation: a promising therapy in autoimmune inflammatory rheumatic diseases.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Review
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  11. Review
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15 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

23 authors at 10 institutions in 4 countries.

L J BlumbergSyntimmune Inc., Boston, MA 02116, USA.ORCID 0000-0002-5647-0672
J E HumphriesBiologics Consulting, Alexandria, VA 22314, USA.
S D JonesBioProcess Technology Consultants, Woburn, MA 01801, USA.
L B PearceBiologics Consulting, Alexandria, VA 22314, USA.
R HolgateAbzena, Babraham, Cambridge, CB22 3AT, UK.
A HearnAbzena, Babraham, Cambridge, CB22 3AT, UK.ORCID 0000-0002-1237-9359
J CheungNew York Structural Biology Center, New York, NY 10027, USA.
A MahmoodNew York Structural Biology Center, New York, NY 10027, USA.ORCID 0000-0003-4779-8358
B Del TitoBiologics Consulting, Alexandria, VA 22314, USA.ORCID 0000-0002-6747-7159
J S GraydonSyntimmune Inc., Boston, MA 02116, USA.
L E StolzSyntimmune Inc., Boston, MA 02116, USA.
A BitontiSyntimmune Inc., Boston, MA 02116, USA.ORCID 0000-0002-1912-7840
S PurohitBioProcess Technology Consultants, Woburn, MA 01801, USA.
D de GraafSyntimmune Inc., Boston, MA 02116, USA.ORCID 0000-0002-7047-256X
K KacenaBioBridges, Wellesley, MA 02481, USA.ORCID 0000-0002-2038-692X
J T AndersenDepartment of Immunology and Centre for Immune Regulation, Oslo University Hospital Rikshospitalet and University of Oslo, Oslo 0424, Norway.
G J ChristiansonThe Jackson Laboratory, Bar Harbor, ME 04609, USA.
D C RoopenianThe Jackson Laboratory, Bar Harbor, ME 04609, USA.
J J HubbardDepartment of Medicine, Division of Gastroenterology, Hepatology and Endoscopy, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
A K GandhiDepartment of Medicine, Division of Gastroenterology, Hepatology and Endoscopy, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
K LasseterClinical Pharmacology of Miami, Miami, FL 33014, USA.ORCID 0000-0001-8175-2199
M PyzikDepartment of Medicine, Division of Gastroenterology, Hepatology and Endoscopy, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.ORCID 0000-0003-2591-6202
R S BlumbergDepartment of Medicine, Division of Gastroenterology, Hepatology and Endoscopy, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.ORCID 0000-0002-9704-248X
Synimmune (Germany) · DEBrigham and Women's Hospital · USInnovative Biologics (United States) · USBabraham Institute · GBGEI Consultants · USJackson Laboratory · USNew York Structural Biology Center · USClinical Pharmacology of Miami · USOslo University Hospital · NOWellesley College · US

Funding

STRUCTURE-FUNCTION RELATIONSHIPS IN THE ALIMENTARY TRACTP30DK034854 · NIDDK · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI JONATHAN C KAGAN · 1986 to 2026
$32.4M
INTESTINAL TRANSCYTOSIS OF IGG IN ADULT LIFER01DK053056 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI BLUMBERG, RICHARD S · 1997 to 2021
$10.6M
Intestinal Immune Regulation by IgG and FcRnR56DK053056 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI BLUMBERG, RICHARD S · 2017 to 2017
$100k
NIDDK NIH HHS P30 DK034854NIDDK NIH HHS R01 DK053056NIDDK NIH HHS R56 DK053056
6 · The paper itself

Abstract

The neonatal crystallizable fragment receptor (FcRn) functions as an intracellular protection receptor for immunoglobulin G (IgG). Recently, several clinical studies have reported the lowering of circulating monomeric IgG levels through FcRn blockade for the potential treatment of autoimmune diseases. Many autoimmune diseases, however, are derived from the effects of IgG immune complexes (ICs). We generated, characterized, and assessed the effects of SYNT001, a FcRn-blocking monoclonal antibody, in mice, nonhuman primates (NHPs), and humans. SYNT001 decreased all IgG subtypes and IgG ICs in the circulation of humans, as we show in a first-in-human phase 1, single ascending dose study. In addition, IgG IC induction of inflammatory pathways was dependent on FcRn and inhibited by SYNT001. These studies expand the role of FcRn in humans by showing that it controls not only IgG protection from catabolism but also inflammatory pathways associated with IgG ICs involved in a variety of autoimmune diseases.

Indexed as

AnimalsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntigen-Antibody ComplexAutoantibodiesAutoimmune DiseasesCohort StudiesDouble-Blind MethodFemaleHealthy VolunteersHistocompatibility Antigens Class IHumansImmunity, HumoralImmunoglobulin GMacaca fascicularisMaleAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntigen-Antibody ComplexAutoantibodiesFc receptor, neonatalHistocompatibility Antigens Class IImmunoglobulin GorilanolimabReceptors, Fc

Identifiers

PMID31897428
PMCPMC6920022
OpenAlexW2994780695

What OpenQuestion holds

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LicenceCC BY-NC
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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.