Evidence map›Paper›PMID 27821811›Full record

ArticleOncotarget2016

Utilization of leukapheresis and CD4 positive selection in Treg isolation and the ex-vivo expansion for a clinical application in transplantation and autoimmune disorders.

Karolina Gołąb, Randall Grose, Piotr Trzonkowski, Amittha Wickrema, Martin Tibudan, Natalia Marek-Trzonkowska, Sabrina Matosz, Julia Solomina, Diane Ostrega, J Michael Millis and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Article
  3. Improving the Efficacy of Regulatory T Cell Therapy.Clinical reviews in allergy & immunology · 2022
    Review
  4. Combined GM-CSF and G-CSF administration mobilizes CD4American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2020
    Article
  5. Article
  6. The immune response is a prerequisite for the development of CD4International journal of clinical and experimental pathology · 2018
    Article
  7. Article
  8. Article
  9. 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

11 authors at 3 institutions in 3 countries.

Karolina GołąbDepartment of Surgery, Section of Transplantation, University of Chicago, Chicago, USA.
Randall GroseSouth Australian Health and Medical Research Institute, University of Adelaide, Australia.
Piotr TrzonkowskiDepartment of Clinical Immunology and Transplantology, Medical University of Gdansk, Gdansk, Poland.
Amittha WickremaDepartment of Medicine, Section of Hematology-Oncology, Cancer Research Center, University of Chicago, Chicago, USA.
Martin TibudanDepartment of Surgery, Section of Transplantation, University of Chicago, Chicago, USA.
Natalia Marek-TrzonkowskaDepartment of Family Medicine, Medical University of Gdansk, Gdansk, Poland.
Sabrina MatoszDepartment of Surgery, Section of Transplantation, University of Chicago, Chicago, USA.
Julia SolominaDepartment of Surgery, Section of Transplantation, University of Chicago, Chicago, USA.
Diane OstregaDepartment of Surgery, Section of Transplantation, University of Chicago, Chicago, USA.
J Michael MillisDepartment of Surgery, Section of Transplantation, University of Chicago, Chicago, USA.
Piotr WitkowskiDepartment of Surgery, Section of Transplantation, University of Chicago, Chicago, USA.
University of Chicago · USGdańsk Medical University · PLSouth Australian Health and Medical Research Institute · AU

Funding

Pilot and Feasibility ProgramP30DK020595 · NIDDK · UNIVERSITY OF CHICAGO · PI Matthew J Brady · 2013 to 2026
$20.9M
Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
NCATS NIH HHS UL1 TR000430NIDDK NIH HHS P30 DK020595
6 · The paper itself

Abstract

Adoptive transfer of T regulatory cells (Tregs) is of great interest as a novel immunosuppressive therapy in autoimmune disorders and transplantation. Obtaining a sufficient number of stable and functional Tregs generated according to current Good Manufacturing Practice (cGMP) requirements has been a major challenge in introducing Tregs as a clinical therapy. Here, we present a protocol involving leukapheresis and CD4+ cell pre-enrichment prior to Treg sorting, which allows a sufficient number of Tregs for a clinical application to be obtained. With this method there is a decreased requirement for ex- vivo expansion. The protocol was validated in cGMP conditions. Our final Treg product passed all release criteria set for clinical applications. Moreover, during expansion Tregs presented their stable phenotype: percentage of CD4+CD25hiCD127- and CD4+FoxP3+ Tregs was > 95% and > 80%, respectively, and Tregs maintained proper immune suppressive function in vitro. Our results suggest that utilization of leukapheresis and CD4 positive selection during Treg isolation improves the likelihood of obtaining a sufficient number of high quality Treg cells during subsequent ex-vivo expansion and they can be applied clinically.

Indexed as

BiomarkersCD4-Positive T-LymphocytesCell SeparationFlow CytometryForkhead Transcription FactorsHumansInterleukin-2 Receptor alpha SubunitInterleukin-7 Receptor alpha SubunitLeukapheresisT-Lymphocytes, RegulatoryBiomarkersForkhead Transcription FactorsFOXP3 protein, humanIL2RA protein, humanInterleukin-2 Receptor alpha SubunitInterleukin-7 Receptor alpha SubunitCD4+ cellsclinical applicationimmunosupressive therapyleukapheresisregulatory T cells

Identifiers

PMID27821811
PMCPMC5346728
OpenAlexW2547176952

What OpenQuestion holds

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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.