Evidence map›Paper›PMID 32030689›Full record

ReviewAdvances in experimental medicine and biology2020

CD200-CD200R Pathway in the Regulation of Tumor Immune Microenvironment and Immunotherapy.

Jin-Qing Liu, Aiyan Hu, Jianmin Zhu, Jianyu Yu, Fatemeh Talebian, Xue-Feng Bai

Open access · greenAbstract readReview
In one paragraph

Review in Advances in experimental medicine and biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
22.9field-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

49 citing papers in PubMed, 69 citations in OpenAlex.

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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

6 authors at 2 institutions in 2 countries.

Jin-Qing LiuDepartment of Pathology, College of Medicine and Comprehensive Cancer Center, Ohio State University, Columbus, OH, USA.
Aiyan HuDepartment of Pathology, College of Medicine and Comprehensive Cancer Center, Ohio State University, Columbus, OH, USA.
Jianmin ZhuDepartment of Pathology, College of Medicine and Comprehensive Cancer Center, Ohio State University, Columbus, OH, USA.
Jianyu YuDepartment of Pathology, College of Medicine and Comprehensive Cancer Center, Ohio State University, Columbus, OH, USA.
Fatemeh TalebianDepartment of Pathology, College of Medicine and Comprehensive Cancer Center, Ohio State University, Columbus, OH, USA.
Xue-Feng BaiDepartment of Pathology, College of Medicine and Comprehensive Cancer Center, Ohio State University, Columbus, OH, USA. Xue-Feng.Bai@osumc.edu.
The Ohio State University · USShanghai Jiao Tong University · CN

Funding

CD200R signaling in tumor growth, immunity and immunotherapyR01CA211014 · NCI · OHIO STATE UNIVERSITY · PI BASU, SUJIT · 2018 to 2022
$1.8M
NCI NIH HHS R01 CA211014
6 · The paper itself

Abstract

Tumor-associated inflammation and immune responses are key components in the tumor microenvironment (TME) which regulate tumor growth, progression, and metastasis. Tumor-associated myeloid cells (TAMCs) are a group of cells that play multiple key roles including induction of tumor-associated inflammation/angiogenesis and regulation of tumor-specific T-cell responses. Thus, identification and characterization of key pathways that can regulate TAMCs are of critical importance for developing cancer immunotherapy. Recent studies suggest that CD200-CD200 receptor (CD200R) interaction may be important in regulating the TME via affecting TAMCs. In this chapter, we will give a brief overview of the CD200-CD200R axis, including the biology behind CD200-CD200R interaction and the role(s) it plays in tumor microenvironment and tumor growth, and activation/effector functions of T cells. We will also discuss CD200-CD200R's role as potential checkpoint molecules for cancer immunotherapy. Further investigation of the CD200-CD200R pathway will not only advance our understanding of tumor pathogenesis and immunity but also provide the rationale for CD200-CD200R-targeted immunotherapy of human cancer.

Indexed as

ImmunotherapyAntigens, CDHumansMyeloid CellsNeoplasmsOrexin ReceptorsTumor MicroenvironmentAntigens, CDantigens, CD200CD200R1 protein, humanOrexin ReceptorsCD200CD200 receptorCytotoxic T lymphocytes (CTLs)Dendritic cells (DCs)ImmunotherapyMyeloid derived suppressor cells (MDSCs)Regulatory T cells (Tregs)Tumor-associated macrophages (TAMs)Tumor-associated myeloid cells (TAMCs)Tumor immunityTumor microenvironment

Identifiers

PMID32030689
PMCPMC7339106
OpenAlexW3004998351

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.