Evidence map›Paper›PMID 27028595›Full record

ArticlePloS one2016

Establishment of a Therapeutic Anti-Pan HLA-Class II Monoclonal Antibody That Directly Induces Lymphoma Cell Death via Large Pore Formation.

Shuji Matsuoka, Yasuyuki Ishii, Atsuhito Nakao, Masaaki Abe, Naomi Ohtsuji, Shuji Momose, Hui Jin, Hisashi Arase, Koichi Sugimoto, Yusuke Nakauchi and 5 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 38% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

15 authors at 7 institutions in 1 country.

Shuji MatsuokaDepartment of Pathology and Oncology, Juntendo University School of Medicine, Tokyo, 113-8421, Japan.
Yasuyuki IshiiRIKEN Research Center for Allergy and Immunology, Yokohama, 204-0022, Japan.
Atsuhito NakaoDepartment of Immunology, Faculty of Medicine, Yamanashi University, Yamanashi, 409-3898, Japan.
Masaaki AbeDepartment of Pathology and Oncology, Juntendo University School of Medicine, Tokyo, 113-8421, Japan.
Naomi OhtsujiDepartment of Pathology and Oncology, Juntendo University School of Medicine, Tokyo, 113-8421, Japan.
Shuji MomoseDepartment of Pathology and Oncology, Juntendo University School of Medicine, Tokyo, 113-8421, Japan.
Hui JinDepartment of Immunochemistry, WPI Immunology Frontier Research Center, Osaka University, Osaka, 565-0871, Japan.
Hisashi AraseDepartment of Immunochemistry, WPI Immunology Frontier Research Center, Osaka University, Osaka, 565-0871, Japan.
Koichi SugimotoDepartment of Hematology and Oncology, JR Tokyo Hospital, Tokyo, 151-8523, Japan.
Yusuke NakauchiDivision of Stem Cell Therapy, Center for Stem Cell Biology and Regenerative Medicine, Institute of Medical Science, The University of Tokyo, Tokyo, 108-8639, Japan.
Hiroshi MasutaniDepartment of Cell Biology, Institute for Virus Research, Kyoto University, Kyoto, 606-8507, Japan.
Michiyuki MaedaDepartment of Cell Biology, Institute for Virus Research, Kyoto University, Kyoto, 606-8507, Japan.
Hideo YagitaDepartment of Immunology, Juntendo University School of Medicine, Tokyo, 113-8421, Japan.
Norio KomatsuDivision of Hematology, Department of Internal Medicine, Juntendo University School of Medicine, Tokyo, 113-8421, Japan.
Okio HinoDepartment of Pathology and Oncology, Juntendo University School of Medicine, Tokyo, 113-8421, Japan.
Juntendo University · JPKyoto University · JPOsaka University · JPJR Tokyo General Hospital · JPRIKEN Center for Integrative Medical Sciences · JPThe University of Tokyo · JPUniversity of Yamanashi · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To develop a new therapeutic monoclonal Antibody (mAb) for Hodgkin lymphoma (HL), we immunized a BALB/c mouse with live HL cell lines, alternating between two HL cell lines. After hybridization, we screened the hybridoma clones by assessing direct cytotoxicity against a HL cell line not used for immunization. We developed this strategy for establishing mAb to reduce the risk of obtaining clonotypic mAb specific for single HL cell line. A newly established mouse anti-human mAb (4713) triggered cytoskeleton-dependent, but complement- and caspase-independent, cell death in HL cell lines, Burkitt lymphoma cell lines, and advanced adult T-cell leukemia cell lines. Intravenous injection of mAb 4713 in tumor-bearing SCID mice improved survival significantly. mAb 4713 was revealed to be a mouse anti-human pan-HLA class II mAb. Treatment with this mAb induced the formation of large pores on the surface of target lymphoma cells within 30 min. This finding suggests that the cell death process induced by this anti-pan HLA-class II mAb may involve the same death signals stimulated by a cytolytic anti-pan MHC class I mAb that also induces large pore formation. This multifaceted study supports the therapeutic potential of mAb 4713 for various forms of lymphoma.

Indexed as

AnimalsAntibodies, MonoclonalAntineoplastic AgentsCell DeathCell Line, TumorCell ShapeCytoskeletonHEK293 CellsHistocompatibility Antigens Class IIHumansMice, Inbred BALB CMice, Inbred ICRMice, SCIDSignal TransductionXenograft Model Antitumor AssaysAntibodies, MonoclonalAntineoplastic AgentsHistocompatibility Antigens Class IImAB4713 monoconal antibody, mouse

Identifiers

PMID27028595
PMCPMC4814124
OpenAlexW2317351834

What OpenQuestion holds

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Registered trials

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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.