Evidence map›Paper›PMID 32167176›Full record

ArticleTransfusion2020

Group O plasma as a media supplement for CAR-T cells and other adoptive T-cell therapies.

Randin C Nelson, Vicki Fellowes, Ping Jin, Hui Liu, Steven L Highfill, Jiaqiang Ren, James Szymanski, Willy A Flegel, David F Stroncek

Open access · greenAbstract readEvaluation Study
In one paragraph

Article in Transfusion, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 98% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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.

Randin C NelsonDepartment of Transfusion Medicine, National Institutes of Health Clinical Center, Bethesda, Maryland.ORCID 0000-0002-0455-1235
Vicki FellowesDepartment of Transfusion Medicine, National Institutes of Health Clinical Center, Bethesda, Maryland.
Ping JinDepartment of Transfusion Medicine, National Institutes of Health Clinical Center, Bethesda, Maryland.
Hui LiuDepartment of Transfusion Medicine, National Institutes of Health Clinical Center, Bethesda, Maryland.
Steven L HighfillDepartment of Transfusion Medicine, National Institutes of Health Clinical Center, Bethesda, Maryland.
Jiaqiang RenDepartment of Transfusion Medicine, National Institutes of Health Clinical Center, Bethesda, Maryland.
James SzymanskiDepartment of Transfusion Medicine, National Institutes of Health Clinical Center, Bethesda, Maryland.
Willy A FlegelDepartment of Transfusion Medicine, National Institutes of Health Clinical Center, Bethesda, Maryland.ORCID 0000-0002-1631-7198
David F StroncekDepartment of Transfusion Medicine, National Institutes of Health Clinical Center, Bethesda, Maryland.
National Institutes of Health Clinical Center · USAlbert Einstein College of Medicine · US

Funding

Development of novel cell and gene therapiesZIACL002120 · CLC · CLINICAL CENTER · PI STRONCEK, DAVID · 2009 to 2025
$0k
Intramural NIH HHS Z99 CL999999Intramural NIH HHS ZIA CL002120
6 · The paper itself

Abstract

backgroundMost chimeric antigen receptor T (CAR-T) cells and other adoptive T-cell therapies (ACTs) are currently manufactured by ex vivo expansion of patient lymphocytes in culture media supplemented with human plasma from group AB donors. As lymphocytes do not express A or B antigens, the isoagglutinins of non-AB plasmas are unlikely to cause deleterious effects on lymphocytes in culture. STUDY DESIGN AND

methodsSeeding cultures with peripheral blood mononuclear cell (PBMNC) concentrates from group A

resultsThere was no difference in lymphocyte expansion or phenotype when cultured with AB plasma or O plasma with high-titer anti-A. Compared to controls, the presence of contaminating RBCs in lymphocyte culture led to poor lymphocyte expansion and a less desirable phenotype-irrespective of the isoagglutinin titer of the plasma supplement used.

conclusionsThis study suggests that ABO incompatible plasma may be used as a media supplement when culturing cell types that do not express ABO antigens-such as lymphocytes for CAR-T or other ACT. The presence of contaminating RBCs in culture was disadvantageous independent of isoagglutinin titer.

Indexed as

Immunotherapy, AdoptiveABO Blood-Group SystemCells, CulturedCulture MediaFlow CytometryHLA-A AntigensHumansLeukocytes, MononuclearLymphocyte ActivationPlasmaPrimary Cell CultureReceptors, Antigen, T-CellReceptors, Chimeric AntigenTissue DonorsT-LymphocytesABO Blood-Group SystemCulture MediaHLA-A AntigensReceptors, Antigen, T-CellReceptors, Chimeric Antigen

Identifiers

PMID32167176
PMCPMC8404615
OpenAlexW3011659153

What OpenQuestion holds

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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.