Evidence map›Paper›PMID 33681468›Full record

ReviewOpen medicine (Warsaw, Poland)2021

The ambiguous role of mannose-binding lectin (MBL) in human immunity.

Namarta Kalia, Jatinder Singh, Manpreet Kaur

Open access · goldAbstract readReview
In one paragraph

Review in Open medicine (Warsaw, Poland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.3field-weighted citation impact, top 4% 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

30 citing papers in PubMed, 70 citations in OpenAlex.

  1. Review
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  6. Review
  7. Gene sequencing andJournal of advanced veterinary and animal research · 2025
    Article
  8. Article
  9. Pathogens (Basel, Switzerland) · 2025
    Article
  10. Article
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  12. Innate Immune Response to Viral Infection.Advances in experimental medicine and biology · 2025
    Review
  13. Review
  14. Article
  15. Article
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  17. Review
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  19. Article
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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

3 authors at 1 institution in 2 countries.

Namarta KaliaDepartment of Molecular Biology and Biochemistry, Guru Nanak Dev University, Amritsar, India.ORCID https://orcid.org/0000-0002-7132-8543
Jatinder SinghDepartment of Molecular Biology and Biochemistry, Guru Nanak Dev University, Amritsar, India.
Manpreet KaurDepartment of Human Genetics, Guru Nanak Dev University, Amritsar, India.
Guru Nanak Dev University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mannose-binding lectin (MBL) and lectin complement pathway have become targets of increasing clinical interest. Many aspects of MBL have been recently explored, including the structural properties that allow it to distinguish self from non-self/altered-self structures. Experimental evidences have declared the additional 5'- and 3'-variants that in amalgamation with well-known secretor polymorphisms change MBL function and concentration. Moreover, the current review highlights the differential behavior of MBL on exposure with extra/intracellular pathogens and in autoimmune diseases, stressing the fact that "high MBL levels can increase diseases susceptibility," a paradox that needs justification. Attributable to these discrepancies, no absolute level of MBL deficiency could be defined so far and thus must be interpreted for specific diseases through case-control population-specific designs. Overall, it is evident that further research is needed about MBL and the lectin pathway of complement. Particularly, the transformative role of MBL over evolution is of interest and its role with regard to pathogenesis of different diseases and potential therapeutic targets within the respective pathways should be further explored. Apart from this, it is necessary to adopt an extensive locus-wide methodology to apprehend the clinical significance of

Indexed as

3′UTR5′ near geneautoimmune diseasesfunctional SNPsinfectious diseasesphagocytosis and MBL patentssingle nucleotide polymorphismsvariants

Identifiers

PMID33681468
PMCPMC7917369
OpenAlexW3133448919

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.