Evidence map›Paper›PMID 28351852›Full record

ReviewJournal of leukocyte biology2017

Leukocyte immunoglobulin-like receptors in human diseases: an overview of their distribution, function, and potential application for immunotherapies.

Jilu Zhang, Sunny Mai, Hui-Ming Chen, Kyeongah Kang, Xian Chang Li, Shu-Hsia Chen, Ping-Ying Pan

Abstract readReview
In one paragraph

Review in Journal of leukocyte biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
–field-weighted citation impact
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

28 citing papers in PubMed.

  1. Article
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  8. Exploring gastric cancer genetics: A turning point in common variable immunodeficiency.The journal of allergy and clinical immunology. Global · 2024
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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.

Jilu ZhangDepartment of Oncological Sciences, Icahn School of Medicine, Mount Sinai, New York, New York, USA.
Sunny MaiDepartment of Oncological Sciences, Icahn School of Medicine, Mount Sinai, New York, New York, USA.
Hui-Ming ChenDepartment of Oncological Sciences, Icahn School of Medicine, Mount Sinai, New York, New York, USA.
Kyeongah KangDepartment of Oncological Sciences, Icahn School of Medicine, Mount Sinai, New York, New York, USA.
Xian Chang LiImmunobiology & Transplant Science Center, Houston Methodist Hospital, Texas Medical Center, Houston, Texas, USA.
Shu-Hsia ChenDepartment of Oncological Sciences, Icahn School of Medicine, Mount Sinai, New York, New York, USA.
Ping-Ying PanDepartment of Oncological Sciences, Icahn School of Medicine, Mount Sinai, New York, New York, USA; ping-ying.pan@mssm.edu.

Funding

Teaching biomedical and pharmacological trainees to produce FAIR data for AI & ML applicationsT32GM062754 · NIGMS · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI SCHLESSINGER, AVNER · 2001 to 2023
$6.2M
Intervention of immune tolerance by small molecules to enhance immune therapyR01CA127483 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI CHEN, SHU-HSIA · 2008 to 2018
$3.4M
Myeloid Suppressor Cell-Mediated Immune Suppression of Tumor Specific T CellsR01CA109322 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CHEN, SHU-HSIA · 2006 to 2015
$3.2M
Modulation of tumor inflammatory factor for immune therapyR01CA208703 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI CHEN, SHU-HSIA · 2017 to 2021
$2.3M
LILRB modulates tumor microenvironment and promotes tumor progressionR01CA204191 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI CHEN, SHU-HSIA · 2017 to 2022
$2.2M
Novel therapy targeting refractory colon cancerR01CA188610 · NCI · METHODIST HOSPITAL RESEARCH INSTITUTE · PI PAN, PING-YING · 2015 to 2019
$1.8M
HSC Derived MDSC for the Prevention of GHVD Without Suppressing GvLR01CA140243 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI PAN, PING-YING · 2011 to 2015
$1.7M
NCI NIH HHS R01 CA109322NCI NIH HHS R01 CA127483NCI NIH HHS R01 CA140243NCI NIH HHS R01 CA188610NCI NIH HHS R01 CA204191NCI NIH HHS R01 CA208703NIGMS NIH HHS T32 GM062754
6 · The paper itself

Abstract

Myeloid-derived suppressor cells (MDSCs), a population of immature myeloid cells expanded and accumulated in tumor-bearing mice and in patients with cancer, have been shown to mediate immune suppression and to promote tumor progression, thereby, posing a major hurdle to the success of immune-activating cancer therapies. MDSCs, like their healthy counterparts, such as monocytes/macrophages and granulocytes, express an array of costimulatory and coinhibitory molecules as well as myeloid activators and inhibitory receptors, such as leukocyte immunoglobulin-like receptors (LILR) A and B. This review summarizes current findings on the LILR family members in various diseases, their potential roles in the pathogenesis, and possible strategies to revert or enhance the suppressive function of MDSCs for the benefit of patients by targeting LILRs.

Indexed as

AnimalsHumansImmunotherapyMyeloid-Derived Suppressor CellsReceptors, ImmunologicTumor EscapeReceptors, ImmunologicautoimmunitycancerinfectionMDSCstransplant tolerance

Identifiers

PMID28351852
PMCPMC5505746

What OpenQuestion holds

Textmetadata
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.