Evidence map›Paper›PMID 42559412›Full record

ArticlePlastic and reconstructive surgery. Global open2026

Human Adipose Allograft Restores Volume Through Host-mediated Tissue Replacement.

Alla Danilkovitch, Molly C Saunders, Samson Tom

Abstract read
In one paragraph

Article in Plastic and reconstructive surgery. Global open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Alla DanilkovitchFrom the Britecyte, Inc., Frederick, MD.
Molly C SaundersFrom the Britecyte, Inc., Frederick, MD.
Samson TomFrom the Britecyte, Inc., Frederick, MD.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Advances in adipose tissue technology have led to the development of a commercial human adipose tissue allograft (hATA) for the restoration of adipose volume; hATA retains native adipose architecture, including structurally intact adipocytes, while eliminating immunogenic components to allow allogeneic use. This study evaluates the mechanisms by which hATA restores volume and the fate of donor-derived human deoxyribonucleic acid (DNA) and proteins following in vivo implantation. Methods: Tissue structure and adipocyte integrity in hATA were evaluated by histology and free lipid analysis. The absence of extracellular damage-associated molecular patterns was assessed by DNA electrophoresis. In vivo remodeling and persistence of human-derived molecules were evaluated in a 12-week nude mouse model. Grafts were evaluated by visual appearance and weight; histology and immunohistochemistry; and the presence of human cells, adiponectin, and DNA. Systemic distribution was evaluated by human adiponectin detection in mouse serum. Results: The hATA lacked immunogenic cells and extracellular damage-associated molecular patterns. Following in vivo implantation, hATA was populated by host-derived cells that remodeled and replaced the graft with host tissue. Human DNA was not detectable beyond 4 weeks, and human proteins progressively degraded. No human molecules were detected in systemic circulation. Conclusions: Use of hATA provides immediate volume restoration through structurally intact adipocytes with retention maintained by host-mediated tissue regeneration. These findings support the graft replacement theory as the mechanism underlying hATA remodeling in vivo.

Identifiers

PMID42559412
PMCPMC13441125

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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.