Evidence map›Paper›PMID 27145284›Full record

ArticleOncotarget2016

Chimeric antigen receptor T cells secreting anti-PD-L1 antibodies more effectively regress renal cell carcinoma in a humanized mouse model.

Eloah Rabello Suarez, De Kuan Chang, Jiusong Sun, Jianhua Sui, Gordon J Freeman, Sabina Signoretti, Quan Zhu, Wayne A Marasco

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 213 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
213citing papers in PubMed, 1 pooled it
12.6field-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.

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

213 citing papers in PubMed, 1 synthesis or guideline pooled it, 326 citations in OpenAlex.

  1. Mapping the clinical landscape of multifunctional CAR T cells: Targets, trends, and synergies.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
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  8. CAR-mediated release of IL-10 increases the function of regulatory T cells: Relevance for future clinical application.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
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  12. Ibrutinib and PD-1 Blockade Potentiate Mesothelin-Targeting CAR T-cell Therapy in Preclinical Models of Pancreatic Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
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153 more citing papers are in PubMed but not listed here.

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

8 authors at 4 institutions in 3 countries.

Eloah Rabello SuarezDepartment of Cancer Immunology and Virology, Dana-Farber Cancer Institute (DFCI), Boston, MA, USA.
De Kuan ChangDepartment of Cancer Immunology and Virology, Dana-Farber Cancer Institute (DFCI), Boston, MA, USA.
Jiusong SunDepartment of Cancer Immunology and Virology, Dana-Farber Cancer Institute (DFCI), Boston, MA, USA.
Jianhua SuiNational Institute of Biological Sciences, ZGC Life Science Park, Changping, Beijing, China.
Gordon J FreemanDepartment of Medicine, Harvard Medical School, Boston, MA, USA.
Sabina SignorettiDepartment of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Quan ZhuDepartment of Cancer Immunology and Virology, Dana-Farber Cancer Institute (DFCI), Boston, MA, USA.
Wayne A MarascoDepartment of Cancer Immunology and Virology, Dana-Farber Cancer Institute (DFCI), Boston, MA, USA.
Dana-Farber Cancer Institute · USHarvard University · USBrigham and Women's Hospital · USNational Institute of Biological Sciences, Beijing · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advances in the treatment of metastatic clear cell renal cell carcinoma (ccRCC) have led to improved progression-free survival of many patients; however the therapies are toxic, rarely achieve durable long-term complete responses and are not curative. Herein we used a single bicistronic lentiviral vector to develop a new combination immunotherapy that consists of human anti-carbonic anhydrase IX (CAIX)-targeted chimeric antigen receptor (CAR) T cells engineered to secrete human anti-programmed death ligand 1 (PD-L1) antibodies at the tumor site. The local antibody delivery led to marked immune checkpoint blockade. Tumor growth diminished 5 times and tumor weight reduced 50-80% when compared with the anti-CAIX CAR T cells alone in a humanized mice model of ccRCC. The expression of PD-L1 and Ki67 in the tumors decreased and an increase in granzyme B levels was found in CAR T cells. The anti-PD-L1 IgG1 isotype, which is capable of mediating ADCC, was also able to recruit human NK cells to the tumor site in vivo. These armed second-generation CAR T cells empowered to secrete human anti-PD-L1 antibodies in the ccRCC milieu to combat T cell exhaustion is an innovation in this field that should provide renewed potential for CAR T cell immunotherapy of solid tumors where limited efficacy is currently seen.

Indexed as

AnimalsAntibodiesAntigens, NeoplasmB7-H1 AntigenCarbonic AnhydrasesCarcinoma, Renal CellCD8-Positive T-LymphocytesCell Line, TumorChimeraDisease Models, AnimalGranzymesHEK293 CellsHumansImmunotherapyKi-67 AntigenKidney NeoplasmsAntibodiesAntigens, NeoplasmB7-H1 AntigenCarbonic AnhydrasesCD274 protein, humanGranzymesGzmb protein, mouseKi-67 AntigenMki67 protein, mouseReceptors, Antigen, T-Cellcarbonic anhydrase IXchimeric antigen receptorimmune checkpoint inhibitorinterleukin-21T cell exhaustion

Identifiers

PMID27145284
PMCPMC5085160
OpenAlexW2342747014

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.