Evidence map›Paper›PMID 31416704›Full record

ReviewCytotherapy2019

Preservation of cell-based immunotherapies for clinical trials.

Rui Li, Rachel Johnson, Guanglin Yu, David H McKenna, Allison Hubel

Open access · greenAbstract readReview
In one paragraph

Review in Cytotherapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
5.2field-weighted citation impact, top 3% 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

51 citing papers in PubMed, 101 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Restoring NK Cell Cytotoxicity Post-Cryopreservation via Synthetic Cells.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Good manufacturing practice production of an off-the-shelf CD34Cellular and molecular life sciences : CMLS · 2025
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. A quest for stakeholder synchronization in the CAR T-cell therapy supply chain.Frontiers in bioengineering and biotechnology · 2024
    Review
  20. 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

5 authors at 1 institution in 1 country.

Rui LiDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, Minnesota, USA.
Rachel JohnsonDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, Minnesota, USA.
Guanglin YuDepartment of Mechanical Engineering, University of Minnesota, Minneapolis, Minnesota, USA.
David H McKennaDepartment of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, Minnesota, USA.
Allison HubelDepartment of Mechanical Engineering, University of Minnesota, Minneapolis, Minnesota, USA. Electronic address: hubel001@umn.edu.
University of Minnesota · US

Funding

Multicomponent solutions for the preservation of cell therapy productsR01EB023880 · NIBIB · UNIVERSITY OF MINNESOTA · PI HUBEL, ALLISON · 2017 to 2019
$1.1M
Integrated training in development and clinical practice of cell-based therapiesR25HL128372 · NHLBI · UNIVERSITY OF MINNESOTA · PI HUBEL, ALLISON, MCKENNA, DAVID HURLEY · 2015 to 2019
$553k
NHLBI NIH HHS R25 HL128372NIBIB NIH HHS R01 EB023880
6 · The paper itself

Abstract

In the unique supply chain of cellular therapies, preservation is important to keep the cell product viable. Many factors in cryopreservation affect the outcome of a cell therapy: (i) formulation and introduction of a freezing medium, (ii) cooling rate, (iii) storage conditions, (iv) thawing conditions and (v) post-thaw processing. This article surveys clinical trials of cellular immunotherapy that used cryopreserved regulatory, chimeric antigen receptor or gamma delta T cells, dendritic cells or natural killer (NK) cells. Several observations are summarized from the given information. The aforementioned cell types have been similarly frozen in media containing 5-10% dimethyl sulfoxide (DMSO) with plasma, serum or human serum albumin. Two common freezing methods are an insulated freezing container such as Nalgene Mr. Frosty and a controlled-rate freezer at a cooling rate of -1°C/min. Water baths at approximately 37°C have been commonly used for thawing. Post-thaw processing of cryopreserved cells varied greatly: some studies infused the cells immediately upon thawing; some diluted the cells in a carrier solution of varying formulation before infusion; some washed cells to remove cryoprotective agents; and others re-cultured cells to recover cell viability or functionality lost due to cryopreservation. Emerging approaches to preserving cellular immunotherapies are also described. DMSO-free formulations of the freezing media have demonstrated improved preservation of cell viability in T lymphocytes and of cytotoxic function in natural killer cells. Saccharides are a common type of molecule used as an alternative cryoprotective agent to DMSO. Improving methods of preservation will be critical to growth in the clinical use of cellular immunotherapies.

Indexed as

Clinical Trials as TopicCryopreservationImmunotherapyCell- and Tissue-Based TherapyDendritic CellsHumansKiller Cells, Naturalcell therapiescryopreservationdendritic cellsnatural killer cellsT cells

Identifiers

PMID31416704
PMCPMC6746578
OpenAlexW2968960744

What OpenQuestion holds

Textmetadata
LicenceTDM
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.