Evidence map›Paper›PMID 24854034›Full record

ArticlePLoS neglected tropical diseases2014

Scabies mite inactive serine proteases are potent inhibitors of the human complement lectin pathway.

Simone L Reynolds, Robert N Pike, Angela Mika, Anna M Blom, Andreas Hofmann, Lakshmi C Wijeyewickrema, Dave Kemp, Katja Fischer

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.7field-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

28 citing papers in PubMed, 51 citations in OpenAlex.

  1. Pathogens (Basel, Switzerland) · 2025
    Article
  2. Article
  3. Scabies.Nature reviews. Disease primers · 2024
    Review
  4. Review
  5. Article
  6. Characterization of a novel galectin inFrontiers in microbiology · 2023
    Article
  7. Article
  8. Article
  9. Article
  10. Pathogens (Basel, Switzerland) · 2021
    Review
  11. Article
  12. Itch in Scabies-What Do We Know?Frontiers in medicine · 2021
    Review
  13. Article
  14. Review
  15. Isoforms of Cathepsin B1 in Neurotropic Schistosomula ofFrontiers in cellular and infection microbiology · 2020
    Article
  16. Article
  17. Review
  18. Review
  19. Article
  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

8 authors at 5 institutions in 3 countries.

Simone L ReynoldsInfectious Diseases Division, QIMR Berghofer Medical Research Institute, Brisbane, Australia.
Robert N PikeDepartment of Biochemistry and Molecular Biology, Monash University, Melbourne, Australia.
Angela MikaDiagnostics Development, Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Anna M BlomDepartment of Laboratory Medicine, Lund University, Malmö, Sweden.
Andreas HofmannStructural Chemistry Program, Eskitis Institute, Griffith University, Brisbane, Australia.
Lakshmi C WijeyewickremaDepartment of Biochemistry and Molecular Biology, Monash University, Melbourne, Australia.
Dave KempInfectious Diseases Division, QIMR Berghofer Medical Research Institute, Brisbane, Australia.
Katja FischerInfectious Diseases Division, QIMR Berghofer Medical Research Institute, Brisbane, Australia.
QIMR Berghofer Medical Research Institute · AUMonash University · AUBernhard Nocht Institute for Tropical Medicine · DEGriffith University · AULund University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Scabies is an infectious skin disease caused by the mite Sarcoptes scabiei and has been classified as one of the six most prevalent epidermal parasitic skin diseases infecting populations living in poverty by the World Health Organisation. The role of the complement system, a pivotal component of human innate immunity, as an important defence against invading pathogens has been well documented and many parasites have an arsenal of anti-complement defences. We previously reported on a family of scabies mite proteolytically inactive serine protease paralogues (SMIPP-Ss) thought to be implicated in host defence evasion. We have since shown that two family members, SMIPP-S D1 and I1 have the ability to bind the human complement components C1q, mannose binding lectin (MBL) and properdin and are capable of inhibiting all three human complement pathways. This investigation focused on inhibition of the lectin pathway of complement activation as it is likely to be the primary pathway affecting scabies mites. Activation of the lectin pathway relies on the activation of MBL, and as SMIPP-S D1 and I1 have previously been shown to bind MBL, the nature of this interaction was examined using binding and mutagenesis studies. SMIPP-S D1 bound MBL in complex with MBL-associated serine proteases (MASPs) and released the MASP-2 enzyme from the complex. SMIPP-S I1 was also able to bind MBL in complex with MASPs, but MASP-1 and MASP-2 remained in the complex. Despite these differences in mechanism, both molecules inhibited activation of complement components downstream of MBL. Mutagenesis studies revealed that both SMIPP-Ss used an alternative site of the molecule from the residual active site region to inhibit the lectin pathway. We propose that SMIPP-Ss are potent lectin pathway inhibitors and that this mechanism represents an important tool in the immune evasion repertoire of the parasitic mite and a potential target for therapeutics.

Indexed as

Amino Acid SequenceAnimalsComplement C1qComplement Pathway, Mannose-Binding LectinHost-Pathogen InteractionsHumansMannose-Binding LectinMannose-Binding Protein-Associated Serine ProteasesMolecular Sequence DataMutagenesis, Site-DirectedMutationSarcoptes scabieiScabiesSequence AlignmentSerine ProteasesComplement C1qMannose-Binding LectinMannose-Binding Protein-Associated Serine ProteasesSerine Proteases

Identifiers

PMID24854034
PMCPMC4031079
OpenAlexW2106160808

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.