Evidence map›Paper›PMID 35881112›Full record

ArticleThe Journal of experimental medicine2022

Developing high-affinity decoy receptors to treat multiple myeloma and diffuse large B cell lymphoma.

Yu Rebecca Miao, Kaushik Thakkar, Can Cenik, Dadi Jiang, Kazue Mizuno, Chenjun Jia, Caiyun Grace Li, Hongjuan Zhao, Anh Diep, Yu Xu and 7 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 32% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Serum sBCMA in primary and secondary antibody deficiency.Clinical and experimental immunology · 2025
    Article
  3. Article
  4. Current status of BAFF targeting immunotherapy in B-cell neoplasm.International journal of clinical oncology · 2024
    Review
  5. Review
  6. Review
  7. 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

17 authors at 4 institutions in 2 countries.

Yu Rebecca Miao *Department of Radiation Oncology, Stanford University, Stanford, CA.ORCID 0000-0002-5848-9924
Kaushik Thakkar *Department of Radiation Oncology, Stanford University, Stanford, CA.ORCID 0000-0002-4900-3371
Can CenikDepartment of Molecular Biosciences, University of Texas at Austin, Austin, TX.ORCID 0000-0001-6370-0889
Dadi JiangDepartment of Radiation Oncology, MD Anderson Cancer Center, Houston, TX.ORCID 0000-0002-0935-3908
Kazue MizunoDepartment of Radiation Oncology, Stanford University, Stanford, CA.ORCID 0000-0001-8636-3141
Chenjun JiaChemPartner Shanghai, Shanghai, China.ORCID 0000-0003-3636-604X
Caiyun Grace LiDepartment of Radiation Oncology, Stanford University, Stanford, CA.ORCID 0000-0001-6452-3538
Hongjuan ZhaoDepartment of Urology, Stanford University, Stanford, CA.ORCID 0000-0001-6083-0370
Anh DiepDepartment of Radiation Oncology, Stanford University, Stanford, CA.ORCID 0000-0001-6202-6394
Yu XuDepartment of Radiation Oncology, Stanford University, Stanford, CA.ORCID 0000-0001-9332-9013
Xin Eric ZhangDepartment of Oncology, Oxford Institute for Radiation Oncology, University of Oxford, Oxford, UK.ORCID 0000-0003-4439-178X
Teddy Tat Chi YangChemPartner Shanghai, Shanghai, China.ORCID 0000-0002-0622-5353
Michaela LiedtkeDepartment of Medicine (Hematology), Stanford University, Stanford, CA.ORCID 0000-0001-8945-5850
Parveen AbidiDepartment of Medicine (Hematology), Stanford University, Stanford, CA.ORCID 0000-0002-8139-4907
Wing-Sze LeungDepartment of Radiation Oncology, Stanford University, Stanford, CA.ORCID 0000-0001-8332-3005
Albert C KoongDepartment of Radiation Oncology, MD Anderson Cancer Center, Houston, TX.ORCID 0000-0001-9824-1643
Amato J GiacciaDepartment of Radiation Oncology, Stanford University, Stanford, CA.ORCID 0000-0002-1940-2750
Stanford University · USThe University of Texas MD Anderson Cancer Center · USUniversity of Oxford · GBThe University of Texas at Austin · US

Funding

Cancer Prevention and Research Institute of Texas RR180042Kimmelman FundMedical Research CouncilSilicon Valley Community FoundationSydney Frank FoundationWelch Foundation F-2027-20200401
6 · The paper itself

Abstract

Disease relapse and treatment-induced immunotoxicity pose significant clinical challenges for patients with hematological cancers. Here, we reveal distinctive requirements for neutralizing TNF receptor ligands APRIL and BAFF and their receptor activity in MM and DLBCL, impacting protein translation and production in MM cells and modulating the translation efficiency of the ATM interactor (ATMIN/ACSIZ). Therapeutically, we investigated the use of BCMA decoy receptor (sBCMA-Fc) as an inhibitor of APRIL and BAFF. While wild-type sBCMA-Fc effectively blocked APRIL signaling in MM, it lacked activity in DLBCL due to its weak BAFF binding. To expand the therapeutic utility of sBCMA-Fc, we engineered an affinity-enhanced mutant sBCMA-Fc fusion molecule (sBCMA-Fc V3) 4- and 500-fold stronger in binding to APRIL and BAFF, respectively. The mutant sBCMA-Fc V3 clone significantly enhanced antitumor activity against both MM and DLBCL. Importantly, we also demonstrated an adequate toxicity profile and on-target mechanism of action in nonhuman primate studies.

Indexed as

Lymphoma, Large B-Cell, DiffuseMultiple MyelomaAnimalsB-Cell Activating FactorB-Cell Maturation AntigenSignal TransductionTransmembrane Activator and CAML Interactor ProteinTumor Necrosis Factor Ligand Superfamily Member 13B-Cell Activating FactorB-Cell Maturation AntigenTransmembrane Activator and CAML Interactor ProteinTumor Necrosis Factor Ligand Superfamily Member 13

Identifiers

PMID35881112
PMCPMC9428257
OpenAlexW4288039335

What OpenQuestion holds

Textmetadata
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.