Evidence map›Paper›PMID 35168213›Full record

ReviewBiomedical materials (Bristol, England)2022

Foreign body response to synthetic polymer biomaterials and the role of adaptive immunity.

Themis R Kyriakides, Hyun-Je Kim, Christy Zheng, Lauren Harkins, Wanyun Tao, Emily Deschenes

Open access · greenAbstract readReview
In one paragraph

Review in Biomedical materials (Bristol, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
7.0field-weighted citation impact, top 3% 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

49 citing papers in PubMed, 78 citations in OpenAlex.

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  15. Integrating mechanical cues inFrontiers in immunology · 2026
    Review
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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

6 authors at 1 institution in 1 country.

Themis R KyriakidesDepartment of Biomedical Engineering, Yale University, New Haven, CT, 06405, United States of America.ORCID 0000-0002-1937-5764
Hyun-Je KimDepartment of Biomedical Engineering, Yale University, New Haven, CT, 06405, United States of America.
Christy ZhengDepartment of Biomedical Engineering, Yale University, New Haven, CT, 06405, United States of America.ORCID 0000-0002-1748-7607
Lauren HarkinsDepartment of Biomedical Engineering, Yale University, New Haven, CT, 06405, United States of America.
Wanyun TaoDepartment of Biomedical Engineering, Yale University, New Haven, CT, 06405, United States of America.
Emily DeschenesDepartment of Biomedical Engineering, Yale University, New Haven, CT, 06405, United States of America.ORCID 0000-0001-8942-1634
Yale University · US

Funding

Bulk metallic glass nanomoulding for glucose sensorsR01DK115969 · NIDDK · YALE UNIVERSITY · PI KYRIAKIDES, THEMIS R · 2018 to 2021
$1.7M
NIDDK NIH HHS R01 DK115969
6 · The paper itself

Abstract

Implanted biomaterials elicit a series of distinct immune and repair-like responses that are collectively known as the foreign body reaction (FBR). These include processes involving innate immune inflammatory cells and wound repair cells that contribute to the encapsulation of biomaterials with a dense collagenous and largely avascular capsule. Numerous studies have shown that the early phase is dominated by macrophages that fuse to form foreign body giant cells that are considered a hallmark of the FBR. With the advent of more precise cell characterization techniques, specific macrophage subsets have been identified and linked to more or less favorable outcomes. Moreover, studies comparing synthetic- and natural-based polymer biomaterials have allowed the identification of macrophage subtypes that distinguish between fibrotic and regenerative responses. More recently, cells associated with adaptive immunity have been shown to participate in the FBR to synthetic polymers. This suggests the existence of cross-talk between innate and adaptive immune cells that depends on the nature of the implants. However, the exact participation of adaptive immune cells, such as T and B cells, remains unclear. In fact, contradictory studies suggest either the independence or dependence of the FBR on these cells. Here, we review the evidence for the involvement of adaptive immunity in the FBR to synthetic polymers with a focus on cellular and molecular components. In addition, we examine the possibility that such biomaterials induce specific antibody responses resulting in the engagement of adaptive immune cells.

Indexed as

Biocompatible MaterialsForeign BodiesAdaptive ImmunityForeign-Body ReactionHumansPolymersBiocompatible MaterialsPolymersadaptive immunitybiocompatibilityforeign bodypolymers

Identifiers

PMID35168213
PMCPMC9159526
OpenAlexW4213050961

What OpenQuestion holds

Textmetadata
LicenceTDM
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.