Evidence map›Paper›PMID 41835536›Full record

ArticleACS omega2026

Electronic Detection of Functional Cellular Immunity Using Enzymatic Metallization.

Yuvraj Rallapalli, Josiah Rudge, Madeline Hoyle, Rebecca Corral, Advaith Nair, Mallika Senthil, Caitlin Costello, Aniruddh Sarkar

Abstract read
In one paragraph

Article in ACS omega, 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. 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

8 authors.

Yuvraj RallapalliWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.
Josiah RudgeWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.
Madeline HoyleWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.
Rebecca CorralWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.
Advaith NairWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.
Mallika SenthilWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.
Caitlin CostelloWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.
Aniruddh SarkarWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.ORCID https://orcid.org/0000-0002-9327-1525

Funding

Microscale Multiplexed Antibody Fc Profiling and Nanoscale Electronic Detection for Rapid and Scalable Point-of-Care Diagnosis of TuberculosisR01AI182322 · NIAID · GEORGIA INSTITUTE OF TECHNOLOGY · PI Aniruddh Sarkar · 2024 to 2026
$1.1M
NIAID NIH HHS R01 AI182322
6 · The paper itself

Abstract

Accurate detection of immune cell function at the single-cell level is needed for diagnostic and research applications, yet conventional methods such as flow cytometry require complex instrumentation and fluorescent labeling which limits their use in resource-poor settings. To address this limitation, we developed Electronic Phenotyping using Impedance Cytometry (EPIC), a platform that combines antibody-directed enzymatic metallization on the cell surface with multifrequency impedance analysis, in a microscale 3D-printed plastic aperture, to electronically detect surface marker-based metallization and cytokine secretion. Using CD45-targeted metallization, EPIC generated distinct impedance signatures in Jurkat cells and primary human peripheral blood mononuclear cells, with impedance changes correlating to surface metallization. A bispecific capture strategy coupled to the metallization was then used for detection of IFN-γ secretion of cells, with impedance readouts matching flow cytometry. These findings demonstrate the ability of the EPIC system for sensitive electronic immune profiling and support its potential as a scalable, low-cost alternative to fluorescence-based assays for point-of-care cellular immunity based diagnostics.

Identifiers

PMID41835536
PMCPMC12980182

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.