Evidence map›Paper›PMID 35302839›Full record

ArticleScience advances2022

Promoting antibody-dependent cellular phagocytosis for effective macrophage-based cancer immunotherapy.

Xu Cao, Jing Chen, Bolei Li, Jessica Dang, Wencan Zhang, Xiancai Zhong, Chongkai Wang, Mustafa Raoof, Zuoming Sun, Jianhua Yu and 2 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed, 1 pooled it
8.4field-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

58 citing papers in PubMed, 1 synthesis or guideline pooled it, 106 citations in OpenAlex.

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  19. Macrophages: sentinels, warriors, and healers.Human molecular genetics · 2025
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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

12 authors at 1 institution in 1 country.

Xu CaoDepartment of Immuno-Oncology, Beckman Research Institute, City of Hope, Duarte, CA 91010, USA.ORCID 0000-0002-9927-6802
Jing ChenDepartment of Immuno-Oncology, Beckman Research Institute, City of Hope, Duarte, CA 91010, USA.ORCID 0000-0002-6022-3914
Bolei LiDepartment of Immuno-Oncology, Beckman Research Institute, City of Hope, Duarte, CA 91010, USA.ORCID 0000-0002-0077-7421
Jessica DangDepartment of Immuno-Oncology, Beckman Research Institute, City of Hope, Duarte, CA 91010, USA.
Wencan ZhangDepartment of Immunology and Theranostics, Arthur Riggs Diabetes and Metabolism Research Institute, Beckman Research Institute, City of Hope, Duarte, CA 91010, USA.
Xiancai ZhongDepartment of Immunology and Theranostics, Arthur Riggs Diabetes and Metabolism Research Institute, Beckman Research Institute, City of Hope, Duarte, CA 91010, USA.ORCID 0000-0001-8312-4057
Chongkai WangDepartment of Medical Oncology and Therapeutics Research, City of Hope, Duarte, CA 91010, USA.ORCID 0000-0002-2186-8875
Mustafa RaoofDepartment of Surgery, City of Hope, Duarte, CA 91010, USA.ORCID 0000-0003-4710-2226
Zuoming SunDepartment of Immunology and Theranostics, Arthur Riggs Diabetes and Metabolism Research Institute, Beckman Research Institute, City of Hope, Duarte, CA 91010, USA.ORCID 0000-0003-1896-6666
Jianhua YuDepartment of Immuno-Oncology, Beckman Research Institute, City of Hope, Duarte, CA 91010, USA.ORCID 0000-0002-0326-3223
Marwan G FakihDepartment of Medical Oncology and Therapeutics Research, City of Hope, Duarte, CA 91010, USA.ORCID 0000-0002-6554-5488
Mingye FengDepartment of Immuno-Oncology, Beckman Research Institute, City of Hope, Duarte, CA 91010, USA.ORCID 0000-0002-3334-9917
City of Hope · US

Funding

Transgenic Mouse FacilityP30CA033572 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI STANLEY R. HAMILTON · 1985 to 2026
$86.3M
Steroid nuclear receptor coactivators in T cell differentiationR01AI109644 · NIAID · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI Zuoming Sun · 2014 to 2026
$6.9M
IL-15--CHARACTERIZATION THROUGH EXPERIMENTAL IMMUNOLOGYR01CA068458 · NCI · ROSWELL PARK CANCER INSTITUTE · PI CALIGIURI, MICHAEL A, YU, JIANHUA · 1996 to 2019
$4.5M
PKC-theta function in RORgammat-regulated Th17 differentiationR01AI053147 · NIAID · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SUN, ZUOMING · 2004 to 2015
$3.7M
Targeting FLT3 for the Treatment of Relapsed or Refractory Acute Myeloid LeukemiaR01CA265095 · NCI · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI BUDDE, LIHUA ELIZABETH, CALIGIURI, MICHAEL A · 2021 to 2025
$2.4M
Characterizing and Targeting the Novel IL-15- AKT-XBP1s Pathway in NK CellsR01CA247550 · NCI · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI YU, JIANHUA · 2020 to 2024
$2.2M
Identifying and engaging a universal adjuvant for breaking macrophage immune tolerance in cancerR01CA255250 · NCI · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI FENG, MINGYE · 2021 to 2025
$2.1M
Elucidate and Modulate Cell Signaling in NK Cells for Glioma TreatmentR01AI129582 · NIAID · OHIO STATE UNIVERSITY · PI YU, JIANHUA · 2017 to 2021
$2.1M
Overcoming Barriers of Virotherapy by Next-Generation oHSV Expressing E-CadherinR01NS106170 · NINDS · OHIO STATE UNIVERSITY · PI YU, JIANHUA · 2018 to 2023
$1.9M
Phase 1 Evaluation of Enhanced Natural Killer Cells as a Treatment Strategy in Non-Small cell Lung Cancer Patients Refractory to PD-1/PD-L1 Immune Checkpoint InhibitorsR01CA266457 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI VILLALONA, MIGUEL A, YU, JIANHUA · 2022 to 2025
$1.8M
scFvPD1-FLT3 CAR T Cells for the Treatment of Relapsed Acute Myeloid LeukemiaR21CA223400 · NCI · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI YU, JIANHUA · 2019 to 2020
$414k
NCI NIH HHS P30 CA033572NCI NIH HHS R01 CA068458NCI NIH HHS R01 CA247550NCI NIH HHS R01 CA255250NCI NIH HHS R01 CA265095NCI NIH HHS R01 CA266457NCI NIH HHS R21 CA223400NIAID NIH HHS R01 AI053147NIAID NIH HHS R01 AI109644NIAID NIH HHS R01 AI129582NINDS NIH HHS R01 NS106170
6 · The paper itself

Abstract

Macrophages are essential in eliciting antibody-dependent cellular phagocytosis (ADCP) of cancer cells. However, a satisfactory anticancer efficacy of ADCP is contingent on early antibody administration, and resistance develops along with cancer progression. Here, we investigate the mechanisms underlying ADCP and demonstrate an effective combinatorial strategy to potentiate its efficacy. We identified paclitaxel as a universal adjuvant that efficiently potentiated ADCP by a variety of anticancer antibodies in multiple cancers. Rather than eliciting cytotoxicity on cancer cells, paclitaxel polarized macrophages toward a state with enhanced phagocytic ability. Paclitaxel-treated macrophages down-regulated cell surface CSF1R whose expression was negatively correlated with patient survival in multiple malignancies. The suppression of CSF1R in macrophages enhanced ADCP of cancer cells, suggesting a role of CSF1R in regulating macrophage phagocytic ability. Together, these findings define a potent strategy for using conventional anticancer drugs to stimulate macrophage phagocytosis and promote the therapeutic efficacy of clinical anticancer antibodies.

Indexed as

MacrophagesNeoplasmsAntibodies, MonoclonalCell Line, TumorHumansImmunotherapyPhagocytosisAntibodies, Monoclonal

Identifiers

PMID35302839
PMCPMC8932662
OpenAlexW4220851646

What OpenQuestion holds

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LicenceCC BY-NC
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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.