Evidence map›Paper›PMID 23797159›Full record

ArticleJournal of innate immunity2014

Thymosin α1 activates complement receptor-mediated phagocytosis in human monocyte-derived macrophages.

Annalucia Serafino, Francesca Pica, Federica Andreola, Roberta Gaziano, Noemi Moroni, Gabriella Moroni, Manuela Zonfrillo, Pasquale Pierimarchi, Paola Sinibaldi-Vallebona, Enrico Garaci

Open access · bronzeAbstract read
In one paragraph

Article in Journal of innate immunity, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.8field-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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Aging and Thymosin Alpha-1.International journal of molecular sciences · 2025
    Review
  3. Therapeutic Potential ofInternational journal of molecular sciences · 2025
    Article
  4. Article
  5. Clinical practice of sepsis-induced immunosuppression: Current immunotherapy and future options.Chinese journal of traumatology = Zhonghua chuang shang za zhi · 2024
    Review
  6. Review
  7. Article
  8. Essential Oil fromMolecules (Basel, Switzerland) · 2022
    Article
  9. Immune therapy in sepsis: Are we ready to try again?Journal of the Intensive Care Society · 2018
    Review
  10. Article
  11. On PAMPs and DAMPs.Journal of innate immunity · 2016
    Article
  12. Foodies of Innate Immunity.Journal of innate immunity · 2015
    Article
  13. 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 3 institutions in 1 country.

Annalucia SerafinoInstitute of Translational Pharmacology, National Research Council of Italy, Rome, Italy.
Francesca Pica
Federica Andreola
Roberta Gaziano
Noemi Moroni
Gabriella Moroni
Manuela Zonfrillo
Pasquale Pierimarchi
Paola Sinibaldi-Vallebona
Enrico Garaci
University of Rome Tor Vergata · ITIstituto di Farmacologia Traslazionale · ITNational Research Council · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thymosin α1 (Tα1) is a naturally occurring thymic peptide used worldwide in clinical trials for the treatment of infectious diseases and cancer. The immunomodulatory activity of Tα1 on innate immunity effector cells has been extensively described, but its mechanism of action is not completely understood. We report that Tα1-exposed human monocyte-derived macrophages (MDMs) assume the typical activated morphology also exhibited by lipopolysaccharide-activated MDMs, but show a comparatively higher ability of internalizing fluorescent beads and zymosan particles. Tα1 exposure also promptly and dramatically stimulates MDM phagocytosis and killing of Aspergillus niger conidia starting as soon as 30 min after challenge. The effect is dose dependent and early coupled to low transcription of the proinflammatory cytokines tumor necrosis factor α and interleukin-6 and unmodified Toll-like receptor expression. The Tα1-stimulated phagocytosis is strictly dependent on the integrity of the microtubule network and protein kinase C activity and occurs by a variation in the classic zipper model, with recruitment of vinculin and actin at the phagosome exhibiting a punctate distribution. These findings indicate that, in human mature MDMs, Tα1 implements pathogen internalization and killing via the stimulation of the complement receptor-mediated phagocytosis. Our observations document that Tα1 is an early and potent activator of innate immunity and reinforce the concept of its pleiotropy.

Indexed as

PhagocytosisActinsAspergillus nigerCells, CulturedComplement ActivationComplement System ProteinsCytotoxicity, ImmunologicDown-RegulationHumansImmunity, InnateInflammation MediatorsInterleukin-6LipopolysaccharidesMacrophagesThymalfasinThymosinActinsComplement System ProteinsInflammation MediatorsInterleukin-6LipopolysaccharidesThymalfasinThymosinTumor Necrosis Factor-alphaVinculinZymosan

Identifiers

PMID23797159
PMCPMC6741600
OpenAlexW2080100768

What OpenQuestion holds

Textmetadata
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.