Evidence map›Paper›PMID 38919628›Full record

ArticleFrontiers in immunology2024

Proof of concept of a new plasma complement Factor H from waste plasma fraction.

Filippo Mori, Giancarlo Pascali, Silvia Berra, Alessandra Lazzarotti, Daniele Panetta, Silvia Rocchiccioli, Elisa Ceccherini, Francesco Norelli, Antonio Morlando, Roberta Donadelli and 5 more

Abstract read
In one paragraph

Article 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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Frontiers in immunology · 2026
    Article
  2. 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

15 authors.

Filippo MoriResearch and Innovation, Kedrion Biopharma, Lucca, Italy.
Giancarlo PascaliBiosciences, Australian Nuclear Science and Technology Organisation, Lucas Heights, NSW, Australia.
Silvia BerraDepartment of Biomedical and Clinical Sciences (DIBIC), University of Milan, Milan, Italy.
Alessandra LazzarottiResearch and Innovation, Kedrion Biopharma, Lucca, Italy.
Daniele PanettaIstituto di Fisiologia Clinica, Consiglio Nazionale delle Ricerche, Pisa, Italy.
Silvia RocchiccioliIstituto di Fisiologia Clinica, Consiglio Nazionale delle Ricerche, Pisa, Italy.
Elisa CeccheriniIstituto di Fisiologia Clinica, Consiglio Nazionale delle Ricerche, Pisa, Italy.
Francesco NorelliIstituto di Fisiologia Clinica, Consiglio Nazionale delle Ricerche, Pisa, Italy.
Antonio MorlandoIstituto di Fisiologia Clinica, Consiglio Nazionale delle Ricerche, Pisa, Italy.
Roberta DonadelliIstituto di Ricerche Farmacologiche Mario Negri IRCCS, Bergamo, Italy.
Alberto ClivioDepartment of Biomedical and Clinical Sciences (DIBIC), University of Milan, Milan, Italy.
Claudio FarinaResearch and Innovation, Kedrion Biopharma, Lucca, Italy.
Marina NorisIstituto di Ricerche Farmacologiche Mario Negri IRCCS, Bergamo, Italy.
Piero A SalvadoriIstituto di Fisiologia Clinica, Consiglio Nazionale delle Ricerche, Pisa, Italy.
Giuseppe RemuzziIstituto di Ricerche Farmacologiche Mario Negri IRCCS, Bergamo, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Complement factor H (FH) is a major regulator of the complement alternative pathway, its mutations predispose to an uncontrolled activation in the kidney and on blood cells and to secondary C3 deficiency. Plasma exchange has been used to correct for FH deficiency and although the therapeutic potential of purified FH has been suggested by Methods: Waste fractions from industrial plasma fractionation (pooled human plasma) were analyzed for FH content by ELISA. FH was purified from unused fraction III and its decay acceleration, cofactor, and C3 binding capacity were characterized Results: Our purification method resulted in a high yield of highly purified (92,07%), pathogen-safe FH. FH concentrate is intact and fully functional as demonstrated by Conclusion: We developed an efficient and economical system for purifying intact and functional FH, starting from waste material of industrial plasma fractionation. The FH concentrate could therefore constitute possible treatments options of patients with C3 glomerulopathy, particularly for those with FH deficiency, but also for patients with other diseases associated with alternative pathway activation.

Indexed as

Complement C3Complement Factor HMice, KnockoutAnimalsDisease Models, AnimalHumansMiceMice, Inbred C57BLProof of Concept StudyCFH protein, humanComplement C3Complement Factor HC3 glomerulopathyconcentrated complement factor H (FH)high-resolution dynamic PETmembrano proliferative glomerulonephritis (MPGN)plasma purification

Identifiers

PMID38919628
PMCPMC11197005

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.