Evidence map›Paper›PMID 40411409›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2025

Sugar Functionalized Collagen Material for Local Modulation of Innate Immunity.

Francesca Taraballi, Claudia Corbo, Julia Enterria-Rosales, John Otto Martinez, Silvia Minardi, Laura Pandolfi, Xing Wang, Ennio Tasciotti, Kavindra V Singh, Cesar A Arias and 1 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2025. 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. Article
  2. Sugar Functionalized Collagen Material for Local Modulation of Innate Immunity.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    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

11 authors.

Francesca TaraballiCenter for Musculoskeletal Regeneration, Houston Methodist Academic Institute, Houston, TX, USA.
Claudia CorboSchool of Medicine and Surgery, Nanomedicine Center Nanomib, University of Milano-Bicocca, Monza, Italy.
Julia Enterria-RosalesCenter for Precision Environmental Health, Baylor College of Medicine, Houston, TX, USA.
John Otto MartinezCenter for Musculoskeletal Regeneration, Houston Methodist Academic Institute, Houston, TX, USA.
Silvia MinardiCenter for Musculoskeletal Regeneration, Houston Methodist Academic Institute, Houston, TX, USA.
Laura PandolfiCenter for Musculoskeletal Regeneration, Houston Methodist Academic Institute, Houston, TX, USA.
Xing WangCenter for Musculoskeletal Regeneration, Houston Methodist Academic Institute, Houston, TX, USA.
Ennio TasciottiCenter for Musculoskeletal Regeneration, Houston Methodist Academic Institute, Houston, TX, USA.
Kavindra V SinghCenter for Infectious Disease, Houston Methodist Research Institute, Houston, TX, USA.
Cesar A AriasCenter for Infectious Disease, Houston Methodist Research Institute, Houston, TX, USA.
Bruna CorradettiCenter for Precision Environmental Health, Baylor College of Medicine, Houston, TX, USA.ORCID https://orcid.org/0000-0002-0345-4847

Funding

Congressionally Directed Medical Research Programs (CDRMP) Discovery Award W81XWH2210048
6 · The paper itself

Abstract

Small alterations during the early stages of the innate immune response to an implant can drive large changes in adaptive immunity. Biomaterials for regenerative purposes can be engineered to modulate this immune response in beneficial ways. This study presents an innovative patch designed and functionalized to target the innate immunity at the implant site. Mannose moieties are incorporated into collagen patches, resulting in a technology called Local Immunotuning Patch (LIP), designed to directly interact with antigen presenting cells through their mannose receptor. In vitro, LIP shows anti-inflammatory effects on bone marrow-derived macrophages and inhibitory properties even on methicillin-resistant bacterial strains. Subcutaneous implantation in mice reveals that LIP modulates multiple pathways related to innate and adaptive immunity, underscoring its role in shaping an immune-engineered environment around the implant. These findings highlight the potential of this strategy to control the foreign body reaction at the implant site, making it applicable for various uses, including wound healing and surgical infection control in reconstructive procedures.

Indexed as

Biocompatible MaterialsCollagenForeign-Body ReactionImmunity, InnateProstheses and ImplantsTissue ScaffoldsAdaptive ImmunityAnimalsCross-Linking ReagentsMacrophagesMannoseMiceMice, Inbred BALB CMice, Inbred C57BLPrimary Cell CultureWound HealingBiocompatible MaterialsCollagenCross-Linking ReagentsMannoseimmunomodulatory patchinnate immunitymannosesugar functionalization

Identifiers

PMID40411409
PMCPMC12376565

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.