Evidence map›Paper›PMID 37879074›Full record

ArticleBlood2024

CD19 occupancy with tafasitamab increases therapeutic index of CART19 cell therapy and diminishes severity of CRS.

R Leo Sakemura, Claudia Manriquez Roman, Paulina Horvei, Elizabeth L Siegler, James H Girsch, Olivia L Sirpilla, Carli M Stewart, Kun Yun, Ismail Can, Ekene J Ogbodo and 21 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Blood, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 5% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
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  8. Article
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  11. Toxicities Associated with CAR-T Cell Therapies.Mediterranean journal of hematology and infectious diseases · 2025
    Review
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  13. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

31 authors at 3 institutions in 2 countries.

R Leo SakemuraT Cell Engineering, Mayo Clinic, Rochester, MN.ORCID 0000-0002-0293-5577
Claudia Manriquez RomanT Cell Engineering, Mayo Clinic, Rochester, MN.ORCID 0000-0003-0082-9735
Paulina HorveiT Cell Engineering, Mayo Clinic, Rochester, MN.ORCID 0009-0006-6774-1542
Elizabeth L SieglerT Cell Engineering, Mayo Clinic, Rochester, MN.ORCID 0000-0002-8336-4373
James H GirschT Cell Engineering, Mayo Clinic, Rochester, MN.ORCID 0000-0003-4592-4015
Olivia L SirpillaT Cell Engineering, Mayo Clinic, Rochester, MN.ORCID 0000-0002-0634-407X
Carli M StewartT Cell Engineering, Mayo Clinic, Rochester, MN.ORCID 0000-0002-2288-2230
Kun YunT Cell Engineering, Mayo Clinic, Rochester, MN.ORCID 0009-0000-2782-8527
Ismail CanT Cell Engineering, Mayo Clinic, Rochester, MN.ORCID 0000-0003-0569-5326
Ekene J OgbodoT Cell Engineering, Mayo Clinic, Rochester, MN.
Mohamad M AdadaT Cell Engineering, Mayo Clinic, Rochester, MN.ORCID 0000-0002-2988-2081
Evandro D BezerraT Cell Engineering, Mayo Clinic, Rochester, MN.ORCID 0000-0002-8978-5697
Lionel Aurelien Kankeu FonkouaT Cell Engineering, Mayo Clinic, Rochester, MN.ORCID 0000-0001-5560-2103
Mehrdad HefaziT Cell Engineering, Mayo Clinic, Rochester, MN.
Michael W RuffT Cell Engineering, Mayo Clinic, Rochester, MN.
Brooke L KimballT Cell Engineering, Mayo Clinic, Rochester, MN.ORCID 0009-0009-3308-2704
Long K MaiT Cell Engineering, Mayo Clinic, Rochester, MN.ORCID 0009-0002-8930-0626
Truc N HuynhT Cell Engineering, Mayo Clinic, Rochester, MN.ORCID 0009-0003-7521-4185
Wendy K NevalaDepartment of Immunology, Mayo Clinic, Rochester, MN.
Kristina IlievaMorphosys AG, Planegg, Germany.ORCID 0000-0002-6877-3793
Christian AugsbergerMorphosys AG, Planegg, Germany.ORCID 0000-0001-7924-2042
Maria Patra-KneuerMorphosys AG, Planegg, Germany.ORCID 0000-0003-4656-0997
Jürgen SchanzerMorphosys AG, Planegg, Germany.
Jan EndellMorphosys AG, Planegg, Germany.
Christina HeitmüllerMorphosys AG, Planegg, Germany.
Stefan SteidlMorphosys AG, Planegg, Germany.ORCID 0000-0003-0048-6859
Sameer A ParikhDivision of Hematology, Mayo Clinic, Rochester, MN.ORCID 0000-0002-3221-7314
Wei DingDivision of Hematology, Mayo Clinic, Rochester, MN.ORCID 0000-0001-9811-4601
Neil E KayDivision of Hematology, Mayo Clinic, Rochester, MN.ORCID 0000-0002-5951-5055
Grzegorz S NowakowskiDivision of Hematology, Mayo Clinic, Rochester, MN.
Saad S KenderianT Cell Engineering, Mayo Clinic, Rochester, MN.ORCID 0000-0003-2767-3830
Mayo Clinic · USMorphoSys (Germany) · DEMayo Clinic in Arizona · US

Funding

Paul Calabresi Program in Clinical/Translational Research at Mayo ClinicK12CA090628 · NCI · MAYO CLINIC ROCHESTER · PI WEROHA, SARAVUT · 2001 to 2025
$19.7M
Towards Safer and More Effective CART Cell Therapy Through the Modulation of Myeloid CytokinesR37CA266344 · NCI · MAYO CLINIC ROCHESTER · PI Saad J. Kenderian · 2022 to 2026
$3.5M
Targeting Cancer-Associated Fibroblasts Prevents Resistance to Chimeric Antigen Receptor T Cell TherapyK99CA273304 · NCI · MAYO CLINIC ROCHESTER · PI SAKEMURA, REONA · 2022 to 2023
$342k
NCI NIH HHS K12 CA090628NCI NIH HHS K99 CA273304NCI NIH HHS R37 CA266344
6 · The paper itself

Abstract

abstractIn the development of various strategies of anti-CD19 immunotherapy for the treatment of B-cell malignancies, it remains unclear whether CD19 monoclonal antibody therapy impairs subsequent CD19-targeted chimeric antigen receptor T-cell (CART19) therapy. We evaluated the potential interference between the CD19-targeting monoclonal antibody tafasitamab and CART19 treatment in preclinical models. Concomitant treatment with tafasitamab and CART19 showed major CD19 binding competition, which led to CART19 functional impairment. However, when CD19+ cell lines were pretreated with tafasitamab overnight and the unbound antibody was subsequently removed from the culture, CART19 function was not affected. In preclinical in vivo models, tafasitamab pretreatment demonstrated reduced incidence and severity of cytokine release syndrome and exhibited superior antitumor effects and overall survival compared with CART19 alone. This was associated with transient CD19 occupancy with tafasitamab, which in turn resulted in the inhibition of CART19 overactivation, leading to diminished CAR T apoptosis and pyroptosis of tumor cells.

Indexed as

Antibodies, Monoclonal, HumanizedImmunotherapyAntigens, CD19Immunotherapy, AdoptiveTherapeutic IndexAntibodies, Monoclonal, HumanizedAntigens, CD19tafasitamab

Identifiers

PMID37879074
PMCPMC10808250
OpenAlexW4387933911

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.