Evidence map›Paper›PMID 38437725›Full record

ArticleBlood2024

CD19-CD28: an affinity-optimized CD28 agonist for combination with glofitamab (CD20-TCB) as off-the-shelf immunotherapy.

Johannes Sam, Thomas Hofer, Christine Kuettel, Christina Claus, Jenny Thom, Sylvia Herter, Guy Georges, Koorosh Korfi, Martin Lechmann, Miro Julian Eigenmann and 29 more

Registry-linked trialOpen 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. It is linked to trial NCT05219513 (An Open-Label, Phase 1 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of RO7443904 in Combination With Glofitamab in Participants With Relapsed/Refractory B-Cell Non-Hodgkin's Lymphoma), which is not on this map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
9.6field-weighted citation impact, top 1% 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.

NCT05219513 phase1terminatednot on this map

An Open-Label, Phase 1 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of RO7443904 in Combination With Glofitamab in Participants With Relapsed/Refractory B-Cell Non-Hodgkin's Lymphoma

TypeinterventionalSponsorHoffmann-La RocheRan2022 to 2024Enrolled53ConditionsLymphoma, Non-HodgkinArmsRO7443904, Glofitamab, Obinutuzumab, Tocilizumab
3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 34 citations in OpenAlex.

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  20. Bispecific Antibodies in Hematologic Malignancies: Attacking the Frontline.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2025
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

39 authors at 3 institutions in 3 countries.

Johannes SamRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.ORCID 0000-0002-7455-0609
Thomas HoferRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
Christine KuettelRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
Christina ClausRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.ORCID 0000-0001-6316-5855
Jenny ThomRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
Sylvia HerterRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.ORCID 0000-0002-2446-696X
Guy GeorgesRoche Innovation Center Munich, Roche Pharma Research and Early Development, Penzberg, Germany.ORCID 0000-0001-5737-006X
Koorosh KorfiRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
Martin LechmannRoche Innovation Center Munich, Roche Pharma Research and Early Development, Penzberg, Germany.
Miro Julian EigenmannRoche Innovation Center Basel, Roche Pharma Research and Early Development, Basel, Switzerland.ORCID 0000-0002-7193-9264
Daniel MarbachRoche Innovation Center Basel, Roche Pharma Research and Early Development, Basel, Switzerland.ORCID 0000-0002-6686-9249
Candice JamoisRoche Innovation Center Basel, Roche Pharma Research and Early Development, Basel, Switzerland.
Katharina LechnerRoche Innovation Center Munich, Roche Pharma Research and Early Development, Penzberg, Germany.
Sreenath M KrishnanRoche Innovation Center Basel, Roche Pharma Research and Early Development, Basel, Switzerland.ORCID 0000-0002-5051-7556
Brenda GaillardRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
Joana MarinhoRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.ORCID 0000-0001-9001-9378
Sven KronenbergRoche Innovation Center Basel, Roche Pharma Research and Early Development, Basel, Switzerland.
Leo KunzRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.ORCID 0000-0001-7332-3343
Sabine WilsonRoche Innovation Center Welwyn, Roche Pharma Research and Early Development, Welwyn Garden City, United Kingdom.
Stefanie BrinerRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.ORCID 0000-0003-1266-4384
Samuel GebhardtRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.ORCID 0009-0005-3246-957X
Ahmet VarolRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
Birte AppeltRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
Valeria NicoliniRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
Dario SpezialeRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
Miriam BezRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
Esther BommerRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
Jan EckmannRoche Innovation Center Munich, Roche Pharma Research and Early Development, Penzberg, Germany.ORCID 0009-0008-0829-9576
Carina HageRoche Innovation Center Munich, Roche Pharma Research and Early Development, Penzberg, Germany.ORCID 0000-0002-5352-0742
Florian LimaniRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
Silvia JenniRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.ORCID 0000-0001-7358-7808
Anne SchoenleRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.ORCID 0009-0005-9825-4643
Marine Le ClechRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
Jean-Baptiste Pierre VallierRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.
Sara ColombettiRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.ORCID 0000-0002-7375-8600
Marina BacacRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.ORCID 0000-0003-0581-9579
Stephan GasserRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.ORCID 0000-0002-5616-0914
Christian KleinRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.ORCID 0000-0001-7594-7280
Pablo UmañaRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Schlieren, Switzerland.ORCID 0000-0001-8206-2771
Roche (Switzerland) · CHRoche Pharma AG (Germany) · DERoche (United Kingdom) · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractEffective T-cell responses not only require the engagement of T-cell receptors (TCRs; "signal 1"), but also the availability of costimulatory signals ("signal 2"). T-cell bispecific antibodies (TCBs) deliver a robust signal 1 by engaging the TCR signaling component CD3ε, while simultaneously binding to tumor antigens. The CD20-TCB glofitamab redirects T cells to CD20-expressing malignant B cells. Although glofitamab exhibits strong single-agent efficacy, adding costimulatory signaling may enhance the depth and durability of T-cell-mediated tumor cell killing. We developed a bispecific CD19-targeted CD28 agonist (CD19-CD28), RG6333, to enhance the efficacy of glofitamab and similar TCBs by delivering signal 2 to tumor-infiltrating T cells. CD19-CD28 distinguishes itself from the superagonistic antibody TGN1412, because its activity requires the simultaneous presence of a TCR signal and CD19 target binding. This is achieved through its engineered format incorporating a mutated Fc region with abolished FcγR and C1q binding, CD28 monovalency, and a moderate CD28 binding affinity. In combination with glofitamab, CD19-CD28 strongly increased T-cell effector functions in ex vivo assays using peripheral blood mononuclear cells and spleen samples derived from patients with lymphoma and enhanced glofitamab-mediated regression of aggressive lymphomas in humanized mice. Notably, the triple combination of glofitamab with CD19-CD28 with the costimulatory 4-1BB agonist, CD19-4-1BBL, offered substantially improved long-term tumor control over glofitamab monotherapy and respective duplet combinations. Our findings highlight CD19-CD28 as a safe and highly efficacious off-the-shelf combination partner for glofitamab, similar TCBs, and other costimulatory agonists. CD19-CD28 is currently in a phase 1 clinical trial in combination with glofitamab. This trial was registered at www.clinicaltrials.gov as #NCT05219513.

Indexed as

Antibodies, BispecificAntigens, CD19Antigens, CD20CD28 AntigensImmunotherapyAnimalsHumansMiceMice, Inbred NODT-LymphocytesXenograft Model Antitumor AssaysAntibodies, BispecificAntigens, CD19Antigens, CD20CD19 molecule, humanCD28 Antigens

Identifiers

PMID38437725
PMCPMC11143537
OpenAlexW4392383798

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.