Evidence map›Paper›PMID 38410512›Full record

ReviewFrontiers in immunology2024

The human factor H protein family - an update.

Noémi Sándor, Andrea E Schneider, Alexandra T Matola, Veronika H Barbai, Dániel Bencze, Hani Hashim Hammad, Alexandra Papp, Dorottya Kövesdi, Barbara Uzonyi, Mihály Józsi

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
5.3field-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

14 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Complement system in cancer: friend or foe of immunotherapy.Journal for immunotherapy of cancer · 2026
    Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. 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

10 authors at 2 institutions in 1 country.

Noémi SándorDepartment of Immunology, ELTE Eötvös Loránd University, Budapest, Hungary.
Andrea E SchneiderDepartment of Immunology, ELTE Eötvös Loránd University, Budapest, Hungary.
Alexandra T MatolaDepartment of Immunology, ELTE Eötvös Loránd University, Budapest, Hungary.
Veronika H BarbaiDepartment of Immunology, ELTE Eötvös Loránd University, Budapest, Hungary.
Dániel BenczeDepartment of Immunology, ELTE Eötvös Loránd University, Budapest, Hungary.
Hani Hashim HammadDepartment of Immunology, ELTE Eötvös Loránd University, Budapest, Hungary.
Alexandra PappDepartment of Immunology, ELTE Eötvös Loránd University, Budapest, Hungary.
Dorottya KövesdiDepartment of Immunology, ELTE Eötvös Loránd University, Budapest, Hungary.
Barbara UzonyiDepartment of Immunology, ELTE Eötvös Loránd University, Budapest, Hungary.
Mihály JózsiDepartment of Immunology, ELTE Eötvös Loránd University, Budapest, Hungary.
Eötvös Loránd University · HUHungarian Research Network

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Complement is an ancient and complex network of the immune system and, as such, it plays vital physiological roles, but it is also involved in numerous pathological processes. The proper regulation of the complement system is important to allow its sufficient and targeted activity without deleterious side-effects. Factor H is a major complement regulator, and together with its splice variant factor H-like protein 1 and the five human factor H-related (FHR) proteins, they have been linked to various diseases. The role of factor H in inhibiting complement activation is well studied, but the function of the FHRs is less characterized. Current evidence supports the main role of the FHRs as enhancers of complement activation and opsonization, i.e., counter-balancing the inhibitory effect of factor H. FHRs emerge as soluble pattern recognition molecules and positive regulators of the complement system. In addition, factor H and some of the FHR proteins were shown to modulate the activity of immune cells, a non-canonical function outside the complement cascade. Recent efforts have intensified to study factor H and the FHRs and develop new tools for the distinction, quantification and functional characterization of members of this protein family. Here, we provide an update and overview on the versatile roles of factor H family proteins, what we know about their biological functions in healthy conditions and in diseases.

Indexed as

Complement Factor HComplement System ProteinsComplement ActivationHumansCFH protein, humanComplement Factor HComplement System Proteinsage-related macular degenerationcancercomplement alternative pathwayFactor Hfactor H-related proteinsinfectioninflammationkidney disease

Identifiers

PMID38410512
PMCPMC10894998
OpenAlexW4391750380

What Socratic 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 Socratic graph.