Evidence map›Paper›PMID 24370984›Full record

ArticleJournal of clinical immunology2014

Longitudinal immune responses and gene expression profiles in type 1 leprosy reactions.

Annemieke Geluk, Krista E van Meijgaarden, Louis Wilson, Kidist Bobosha, Jolien J van der Ploeg-van Schip, Susan J F van den Eeden, Edwin Quinten, Karin Dijkman, Kees L M C Franken, Elisabeth M Haisma and 3 more

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Article in Journal of clinical immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 2 pooled it
3.8field-weighted citation impact, top 6% 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, 2 syntheses or guidelines pooled it, 68 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Anti-phenolic glycolipid antibodies inOne health (Amsterdam, Netherlands) · 2025
    Article
  6. Article
  7. Leprosy.Nature reviews. Disease primers · 2024
    Review
  8. Frontiers in microbiology · 2023
    Article
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  13. 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

13 authors at 2 institutions in 2 countries.

Annemieke GelukDepartment of Infectious Diseases, Leiden University Medical Center, PO Box 9600, 2300 RC, Leiden, The Netherlands, ageluk@lumc.nl.
Krista E van Meijgaarden
Louis Wilson
Kidist Bobosha
Jolien J van der Ploeg-van Schip
Susan J F van den Eeden
Edwin Quinten
Karin Dijkman
Kees L M C Franken
Elisabeth M Haisma
Mariëlle C Haks
Colette L M van Hees
Tom H M Ottenhoff
Leiden University Medical Center · NLErasmus MC · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeLeprosy, a chronic disease initiated by Mycobacterium leprae, is often complicated by acute inflammatory reactions. Although such episodes occur in at least 50% of all leprosy patients and may cause irreversible nerve damage, no laboratory tests are available for early diagnosis or prediction of reactions. Since immune- and genetic host factors are critical in leprosy reactions, we hypothesize that identification of host-derived biomarkers correlated to leprosy reactions can provide the basis for new tests to facilitate timely diagnosis and treatment thereby helping to prevent tissue damage.

methodsThe longitudinal host response of a leprosy patient, who was affected by a type 1 reaction (T1R) after MDT-treatment, was studied in unprecedented detail, measuring cellular and humoral immunity and gene expression profiles to identify biomarkers specific for T1R.

resultsCytokine analysis in response to M. leprae revealed increased production of IFN-γ, IP-10, CXCL9, IL-17A and VEGF at diagnosis of T1R compared to before T1R, whereas a simultaneous decrease in IL-10 and G-CSF was observed at T1R. Cytokines shifts coincided with a reduction in known regulatory CD39(+)CCL4(+) and CD25(high) T-cell subsets. Moreover, RNA expression profiles revealed that IFN-induced genes, (V)EGF, and genes associated with cytotoxic T-cell responses (GNLY, GZMA/B, PRF1) were upregulated during T1R, whereas expression of T-cell regulation-associated genes were decreased.

conclusionsThese data show that increased inflammation, vasculoneogenesis and cytotoxicity, perturbed T-cell regulation as well as IFN-induced genes play an important role in T1R and provide potential T1R-specific host biomarkers.

Indexed as

TranscriptomeAdolescentAntigens, BacterialBiomarkersBiopsyCytokinesGene Expression ProfilingGene Expression RegulationHumansImmunity, CellularImmunity, HumoralImmunophenotypingLeprosyMaleMycobacterium lepraeRNA, MessengerAntigens, BacterialBiomarkersCytokinesRNA, Messenger

Identifiers

PMID24370984
OpenAlexW2095397983

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.