Evidence map›Paper›PMID 34984106›Full record

ArticleCell & gene therapy insights2018

Clinical Applications of Regulatory T cells in Adoptive Cell Therapies.

Gregory P Marshall, Judit Cserny, Daniel J Perry, Wen-I Yeh, Howard R Seay, Ahmed G Elsayed, Amanda L Posgai, Todd M Brusko

Abstract read
In one paragraph

Article in Cell & gene therapy insights, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Human CD4Frontiers in immunology · 2022
    Article
  9. Article
  10. 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.

Gregory P MarshallOneVax LLC, Sid Martin Biotechnology Institute, Alachua, Florida, USA.
Judit CsernyDepartment of Pathology, Immunology, and Laboratory Medicine, University of Florida Diabetes Institute, Gainesville, Florida, USA.
Daniel J PerryDepartment of Pathology, Immunology, and Laboratory Medicine, University of Florida Diabetes Institute, Gainesville, Florida, USA.
Wen-I YehDepartment of Pathology, Immunology, and Laboratory Medicine, University of Florida Diabetes Institute, Gainesville, Florida, USA.
Howard R SeayDepartment of Pathology, Immunology, and Laboratory Medicine, University of Florida Diabetes Institute, Gainesville, Florida, USA.
Ahmed G ElsayedDepartment of Pathology, Immunology, and Laboratory Medicine, University of Florida Diabetes Institute, Gainesville, Florida, USA.
Amanda L PosgaiDepartment of Pathology, Immunology, and Laboratory Medicine, University of Florida Diabetes Institute, Gainesville, Florida, USA.
Todd M BruskoOneVax LLC, Sid Martin Biotechnology Institute, Alachua, Florida, USA.

Funding

The CD226 costimulatory axis in type 1 diabetesR01DK106191 · NIDDK · UNIVERSITY OF FLORIDA · PI Todd Michael Brusko · 2016 to 2026
$4.4M
Delivery of biomaterial-conjugated regulatory T Cells for the amelioration of Type 1 DiabetesR21AI133067 · NIAID · ONEVAX, LLC · PI MARSHALL, GREGORY PAUL · 2017 to 2018
$256k
Biomaterial-based delivery of Interleukin-2 to Regulatory T Cells for the amelioration of Type 1 DiabetesR43AI131850 · NIAID · ONEVAX, LLC · PI MARSHALL, GREGORY PAUL · 2017 to 2017
$236k
NIAID NIH HHS R21 AI133067NIAID NIH HHS R43 AI131850NIDDK NIH HHS R01 DK106191
6 · The paper itself

Abstract

Interest in adoptive T-cell therapies has been ignited by the recent clinical success of genetically-modified T cells in the cancer immunotherapy space. In addition to immune targeting for malignancies, this approach is now being explored for the establishment of immune tolerance with regulatory T cells (Tregs). Herein, we will summarize the basic science and clinical results emanating from trials directed at inducing durable immune regulation through administration of Tregs. We will discuss some of the current challenges facing the field in terms of maximizing cell purity, stability and expansion capacity, while also achieving feasibility and GMP production. Indeed, recent advances in methodologies for Treg isolation, expansion, and optimal source materials represent important strides toward these considerations. Finally, we will review the emerging genetic and biomaterial-based approaches on the horizon for directing Treg specificity to augment tissue-targeting and regenerative medicine.

Identifiers

PMID34984106
PMCPMC8722436

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.