Evidence map›Paper›PMID 28390927›Full record

ArticleJournal of immunological methods2017

A novel hemolytic complement-sufficient NSG mouse model supports studies of complement-mediated antitumor activity in vivo.

Mohit K Verma, Julia Clemens, Lisa Burzenski, Stephen B Sampson, Michael A Brehm, Dale L Greiner, Leonard D Shultz

Abstract read
In one paragraph

Article in Journal of immunological methods, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

30 citing papers in PubMed, 42 citations in OpenAlex.

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  5. Transgenic expression of human CD47 on pig cells provides only partial protection against human macrophage-mediated destruction in human immune system mice.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2026
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  6. Humanized mice enableMolecular therapy. Advances · 2026
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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

7 authors at 2 institutions in 1 country.

Mohit K VermaThe Jackson Laboratory, Bar Harbor, ME, United States.
Julia ClemensThe Jackson Laboratory, Bar Harbor, ME, United States.
Lisa BurzenskiThe Jackson Laboratory, Bar Harbor, ME, United States.
Stephen B SampsonThe Jackson Laboratory, Bar Harbor, ME, United States.
Michael A BrehmDiabetes Center of Excellence™, Department of Molecular Medicine, University of Massachusetts Medical School, Worcester, MA, United States.
Dale L GreinerDiabetes Center of Excellence™, Department of Molecular Medicine, University of Massachusetts Medical School, Worcester, MA, United States.
Leonard D ShultzThe Jackson Laboratory, Bar Harbor, ME, United States. Electronic address: lenny.shultz@jax.org.
Jackson Laboratory · USUniversity of Massachusetts Chan Medical School · US

Funding

Shared Resource ManagementP30CA034196 · NCI · JACKSON LABORATORY · PI Jeffrey Hsu-Min Chuang · 1985 to 2026
$61.9M
Tissue Repository and Animal Models CoreP01CA171983 · NCI · UNIVERSITY OF VIRGINIA · PI CLAXTON, DAVID F · 2013 to 2024
$19.9M
Humanized Mouse Avatars for T1DUC4DK104218 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BREHM, MICHAEL ALLEN, DALEY, GEORGE Q · 2014 to 2014
$4.1M
Development and Validation of Novel NSG Mouse Models for Human Stem Cell TherapyR24OD018259 · OD · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BREHM, MICHAEL ALLEN, GREINER, DALE LESLIE · 2014 to 2017
$3.0M
Summer Research Experience in Cancer Biology and Genomics for UndergraduatesR25CA174584 · NCI · JACKSON LABORATORY · PI SHULTZ, LEONARD · 2013 to 2017
$243k
NCI NIH HHS P01 CA171983NCI NIH HHS P30 CA034196NCI NIH HHS R25 CA174584NIDDK NIH HHS UC4 DK104218NIH HHS R24 OD018259
6 · The paper itself

Abstract

Monoclonal antibodies (mAbs) have emerged as a mainstream therapeutic option against cancer. mAbs mediate tumor cell-killing through several mechanisms including complement-dependent cytotoxicity (CDC). However, studies of mAb-mediated CDC against tumor cells remain largely dependent on in vitro systems. Previously developed and widely used NOD-scid IL2rγ

Indexed as

AnimalsAntibodies, MonoclonalAntibodies, Monoclonal, Murine-DerivedAntibody-Dependent Cell CytotoxicityAntigens, CD20Cell Line, TumorComplement System ProteinsDisease Models, AnimalHeterograftsImmunotherapyMiceMice, Inbred NODMice, SCIDRituximabAntibodies, MonoclonalAntibodies, Monoclonal, Murine-DerivedAntigens, CD20Complement System ProteinsRituximabComplement-dependent cytotoxicity (CDC)ImmunotherapyMonoclonal antibody (mAb)NSG micePatient-derived xenograft (PDX)

Identifiers

PMID28390927
PMCPMC5480316
OpenAlexW2604167679

What OpenQuestion holds

Textmetadata
LicenceTDM
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.