Evidence map›Paper›PMID 36672628›Full record

ArticleBiomedicines2023

Immunomodulatory Effects of Non-Thermal Plasma in a Model for Latent HIV-1 Infection: Implications for an HIV-1-Specific Immunotherapy.

Hager Mohamed, Rachel Berman, Jennifer Connors, Elias K Haddad, Vandana Miller, Michael R Nonnemacher, Will Dampier, Brian Wigdahl, Fred C Krebs

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2023. 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
1.4field-weighted citation impact, top 21% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. 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

9 authors at 2 institutions in 1 country.

Hager MohamedDepartment of Microbiology and Immunology, Drexel University College of Medicine, Philadelphia, PA 19102, USA.
Rachel BermanDepartment of Microbiology and Immunology, Drexel University College of Medicine, Philadelphia, PA 19102, USA.
Jennifer ConnorsDepartment of Microbiology and Immunology, Drexel University College of Medicine, Philadelphia, PA 19102, USA.ORCID 0000-0001-9137-0717
Elias K HaddadDepartment of Microbiology and Immunology, Drexel University College of Medicine, Philadelphia, PA 19102, USA.
Vandana MillerDepartment of Microbiology and Immunology, Drexel University College of Medicine, Philadelphia, PA 19102, USA.ORCID 0000-0002-2323-2299
Michael R NonnemacherDepartment of Microbiology and Immunology, Drexel University College of Medicine, Philadelphia, PA 19102, USA.
Will DampierDepartment of Microbiology and Immunology, Drexel University College of Medicine, Philadelphia, PA 19102, USA.
Brian WigdahlDepartment of Microbiology and Immunology, Drexel University College of Medicine, Philadelphia, PA 19102, USA.ORCID 0000-0002-5211-0936
Fred C KrebsDepartment of Microbiology and Immunology, Drexel University College of Medicine, Philadelphia, PA 19102, USA.ORCID 0000-0002-1530-4432
Institute for Molecular Medicine · USDrexel University · US

Funding

Gene editing strategies to target HIV for elimination in periphery and brainR01MH110360 · NIMH · DREXEL UNIVERSITY · PI Ilker Kudret Sariyer, Brian Wigdahl · 2016 to 2026
$7.3M
NIMH NIH HHS R01 MH110360
6 · The paper itself

Abstract

In people living with HIV-1 (PLWH), antiretroviral therapy (ART) eventually becomes necessary to suppress the emergence of human immunodeficiency virus type 1 (HIV-1) replication from latent reservoirs because HIV-1-specific immune responses in PLWH are suboptimal. Immunotherapies that enhance anti-HIV-1 immune responses for better control of virus reemergence from latent reservoirs are postulated to offer ART-free control of HIV-1. Toward the goal of developing an HIV-1-specific immunotherapy based on non-thermal plasma (NTP), the early immunological responses to NTP-exposed latently infected T lymphocytes were examined. Application of NTP to the J-Lat T-lymphocyte cell line (clones 10.6 and 15.4) stimulated monocyte recruitment and macrophage maturation, which are key steps in initiation of an immune response. In contrast, CD8+ T lymphocytes in a mixed lymphocyte reaction assay were not stimulated by the presence of NTP-exposed J-Lat cells. Furthermore, co-culture of NTP-exposed J-Lat cells with mature phagocytes did not modulate their antigen presentation to primary CD8+ T lymphocytes (cross-presentation). However, reactivation from latency was stimulated in a clone-specific manner by NTP. Overall, these studies, which demonstrated that ex vivo application of NTP to latently infected lymphocytes can stimulate key immune cell responses, advance the development of an NTP-based immunotherapy that will provide ART-free control of HIV-1 reactivation in PLWH.

Indexed as

chemotaxisHIV-1immunomodulationlatencylow temperature plasma (LTP)non-thermal plasma (NTP)people living with HIV (PLWH)reactivation

Identifiers

PMID36672628
PMCPMC9856147
OpenAlexW4313584173

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.