Evidence map›Paper›PMID 20004774›Full record

ReviewThe Journal of allergy and clinical immunology2009

Therapy of autoinflammatory syndromes.

Hal M Hoffman

Open access · greenAbstract readReview
In one paragraph

Review in The Journal of allergy and clinical immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
4.3field-weighted citation impact, top 5% 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

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 92 citations in OpenAlex.

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  8. The NLRP1 inflammasome in skin diseases.Frontiers in immunology · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

1 author at 1 institution in 1 country.

Hal M HoffmanDepartment of Pediatrics and Medicine, Division of Allergy, Immunology, and Rheumatology, University of California at San Diego, School of Medicine, 9500 Gilman Dr, La Jolla, CA 92093-0635, USA. hahoffman@ucsd.edu
University of California, San Diego · US

Funding

The Role of Cryopyrin in Autoinflammatory DiseasesR01AI052430 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HOFFMAN, HAROLD M · 2002 to 2011
$3.4M
NIAID NIH HHS R01 AI052430
6 · The paper itself

Abstract

The therapy of autoinflammatory syndromes is an excellent example of the power of translational research. Recent advances in our understanding of the molecular and immunologic basis of this newly identified classification of disease have allowed for the application of novel, effective, targeted treatments with life-changing effects on patients. Although colchicine and TNF-alpha inhibitors are important therapies for specific autoinflammatory syndromes, the novel IL-1-targeted drugs are particularly effective for many of these diseases. Recently, the pharmaceutical industry has adopted a strategy of confirming the efficacy of new targeted drugs in often-ignored patients with orphan diseases, and US Food and Drug Administration policies have allowed for accelerated approval of these drugs, creating a win-win situation for patients and industry. This article reviews the general approach to the therapy of autoinflammatory diseases, focusing on current approved therapies and novel approaches that might be used in the future.

Indexed as

Antirheumatic AgentsAutoantibodiesAutoimmune DiseasesAutoimmunityClinical Trials as TopicColchicineHereditary Autoinflammatory DiseasesHumansInterleukin-1betaInterleukin 1 Receptor Antagonist ProteinSyndromeTubulin ModulatorsTumor Necrosis Factor-alphaAntirheumatic AgentsAutoantibodiesColchicineInterleukin-1betaInterleukin 1 Receptor Antagonist ProteinTubulin ModulatorsTumor Necrosis Factor-alpha

Identifiers

PMID20004774
PMCPMC4508191
OpenAlexW2050781159

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.