Evidence map›Paper›PMID 21119019›Full record

ReviewMicrobiology and molecular biology reviews : MMBR2010

Leprosy and the human genome.

Elizabeth A Misch, William R Berrington, James C Vary, Thomas R Hawn

Open access · greenAbstract readReview
In one paragraph

Review in Microbiology and molecular biology reviews : MMBR, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
4.6field-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

45 citing papers in PubMed, 123 citations in OpenAlex.

  1. Article
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  18. Infection with Mycobacterium lepromatosis.The American journal of tropical medicine and hygiene · 2016
    Article
  19. Review
  20. Article
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

4 authors at 1 institution in 1 country.

Elizabeth A MischDepartment of Medicine, University of Washington School of Medicine, Seattle, Washington 98195, USA.
William R Berrington
James C Vary
Thomas R Hawn
University of Washington · US

Funding

HOST DEFENSE TRAINING IN ALLERGY AND INFECTIOUS DISEASEST32AI007044 · NIAID · UNIVERSITY OF WASHINGTON · PI DAVID Neal FREDRICKS · 1985 to 2026
$14.6M
TLR 1 Variation and the immune Response to Mycobacterium tuberculosisK08AI076604 · NIAID · UNIVERSITY OF WASHINGTON · PI MISCH, ELIZABETH ANN · 2009 to 2013
$753k
The Role of Nod1 and Nod2 in the Pathogeneisis of Legionella Pneumophila PneumoniK08AI080952 · NIAID · UNIVERSITY OF WASHINGTON · PI BERRINGTON, WILLIAM RICHARD · 2009 to 2012
$623k
Polymorphisms of the innate immune system in leprosyF32AR057293 · NIAMS · UNIVERSITY OF WASHINGTON · PI VARY, JAMES C · 2009 to 2009
$55k
NIAID NIH HHS K08 AI076604NIAID NIH HHS K08 AI080952NIAID NIH HHS T32 AI007044NIAMS NIH HHS F32 AR057293NIAMS NIH HHS F32AR057293-01
6 · The paper itself

Abstract

Despite the availability of effective treatment for several decades, leprosy remains an important medical problem in many regions of the world. Infection with Mycobacterium leprae can produce paucibacillary disease, characterized by well-formed granulomas and a Th1 T-cell response, or multibacillary disease, characterized by poorly organized cellular infiltrates and Th2 cytokines. These diametric immune responses confer states of relative resistance or susceptibility to leprosy, respectively, and have well-defined clinical manifestations. As a result, leprosy provides a unique opportunity to dissect the genetic basis of human in vivo immunity. A series of studies over the past 40 years suggests that host genes influence the risk of leprosy acquisition and the predilection for different clinical forms of the disease. However, a comprehensive, cellular, and molecular view of the genes and variants involved is still being assembled. In this article, we review several decades of human genetic studies of leprosy, including a number of recent investigations. We emphasize genetic analyses that are validated by the replication of the same phenotype in independent studies or supported by functional experiments demonstrating biological mechanisms of action for specific polymorphisms. Identifying and functionally exploring the genetic and immunological factors that underlie human susceptibility to leprosy have yielded important insights into M. leprae pathogenesis and are likely to advance our understanding of the immune response to other pathogenic mycobacteria. This knowledge may inform new treatment or vaccine strategies for leprosy or tuberculosis.

Indexed as

Genome, HumanGenetic LinkageGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansLeprosyMycobacterium leprae

Identifiers

PMID21119019
PMCPMC3008172
OpenAlexW2096402478

What OpenQuestion holds

Textmetadata
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.