Evidence map›Paper›PMID 42630643›Full record

ArticleAdvanced functional materials2026

Germanane Quantum Dots Promote Metabolic Reprogramming of Immune Cells Toward Regulatory T Cells and Suppress Inflammation In Vitro and In Vivo.

Abhay Srivastava, Alireza Rafieerad, Weiang Yan, Keshav Narayan Alagarsamy, Qingdong Guan, Leena Regi Saleth, Michel Aliani, Sanjiv Dhingra

Abstract read
In one paragraph

Article in Advanced functional materials, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

8 authors.

Abhay SrivastavaInstitute of Cardiovascular Sciences Department of Physiology and Pathophysiology Rady Faculty of Health Sciences St. Boniface Hospital Albrechtsen Research Centre Biomedical Engineering Program University of Manitoba Winnipeg Manitoba Canada.
Alireza RafieeradInstitute of Cardiovascular Sciences Department of Physiology and Pathophysiology Rady Faculty of Health Sciences St. Boniface Hospital Albrechtsen Research Centre Biomedical Engineering Program University of Manitoba Winnipeg Manitoba Canada.
Weiang YanInstitute of Cardiovascular Sciences Department of Physiology and Pathophysiology Rady Faculty of Health Sciences St. Boniface Hospital Albrechtsen Research Centre Biomedical Engineering Program University of Manitoba Winnipeg Manitoba Canada.
Keshav Narayan AlagarsamyInstitute of Cardiovascular Sciences Department of Physiology and Pathophysiology Rady Faculty of Health Sciences St. Boniface Hospital Albrechtsen Research Centre Biomedical Engineering Program University of Manitoba Winnipeg Manitoba Canada.
Qingdong GuanDepartment of Immunology and Internal Medicine Manitoba Blood and Marrow Transplant Program CancerCare Manitoba University of Manitoba Winnipeg Canada.
Leena Regi SalethInstitute of Cardiovascular Sciences Department of Physiology and Pathophysiology Rady Faculty of Health Sciences St. Boniface Hospital Albrechtsen Research Centre Biomedical Engineering Program University of Manitoba Winnipeg Manitoba Canada.
Michel AlianiDivision of Neurodegenerative Disorders St. Boniface General Hospital Albrechtsen Research Centre University of Manitoba Winnipeg Canada.
Sanjiv DhingraInstitute of Cardiovascular Sciences Department of Physiology and Pathophysiology Rady Faculty of Health Sciences St. Boniface Hospital Albrechtsen Research Centre Biomedical Engineering Program University of Manitoba Winnipeg Manitoba Canada.ORCID https://orcid.org/0000-0002-2664-7633

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, nanomaterials have emerged as a tool in developing novel therapies against inflammatory diseases. Metabolic changes in immune cells direct the phenotype and function of the host immune system. Therefore, next-generation immunomodulatory biomaterials should be designed to target metabolic pathways and trigger specific changes in immune cells to direct their fate toward an anti-inflammatory phenotype. The current study reports the fabrication and first application of germanane quantum dots (GeHQDs) to modulate inflammation in cell culture and in vivo mouse model. Using rational design and synthesis strategies, our GeHQDs leverage the intrinsic anti-inflammatory properties of germanane to provide a novel nanoplatform to trigger metabolic reprogramming of immune cells toward an anti-inflammatory phenotype. These GeHQDs are spontaneously uptaken into the immune cells and trigger a switch in their phenotype toward regulatory T (Treg) cells. Metabolomic analysis suggested a downregulation in glycolytic flux and upregulation in fatty acid oxidation with an increase in mitochondrial respiration in the GeHQDs-treated group, which is a typical signature of Treg cells. In an in vivo mouse model of systemic inflammation, GeHQDs treatment upregulated the circulating Treg cell number, improved the metabolomic profile and downregulated inflammation. The current study presents a new paradigm in targeting inflammatory diseases by modulating immune cell metabolism using next-generation nanomaterials.

Indexed as

immunomodulationmetabolic reprogrammingnanomaterialsquantum dotsregulatory T cellssea‐horse analysis

Identifiers

PMID42630643
PMCPMC13494919

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.