Evidence map›Paper›PMID 33193299›Full record

ReviewFrontiers in immunology2020

Duality of B Cell-CXCL13 Axis in Tumor Immunology.

Angel J Rubio, Tyrone Porter, Xuemei Zhong

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.2field-weighted citation impact, top 10% 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

31 citing papers in PubMed, 41 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

3 authors at 2 institutions in 1 country.

Angel J RubioDepartment of Pharmacology and Experimental Therapeutics, Boston University, Boston, MA, United States.
Tyrone PorterDepartment of Biomedical Engineering, University of Texas Austin, Austin, TX, United States.
Xuemei ZhongHematology and Medical Oncology Section, Department of Medicine, Boston University School of Medicine, Boston, MA, United States.
Boston University · USThe University of Texas at Austin · US

Funding

Development of a novel cell-based immune therapy using Nanoparticles and natural IgM-producing phagocytic B cellsR21CA205415 · NCI · BOSTON MEDICAL CENTER · PI ZHONG, XUEMEI · 2016 to 2017
$428k
NCI NIH HHS R21 CA205415
6 · The paper itself

Abstract

Tumor immunity is a rapidly evolving area of research consisting of many possible permutations of immune cell tumor interactions that are dependent upon cell type, tumor type, and stage in tumor progression. At the same time, the majority of cancer immunotherapies have been focused on modulating the T cell-mediated antitumor immune response and have largely ignored the potential utility that B cells possess with respect to tumor immunity. Therefore, this motivated an exploration into the role that B cells and their accompanying chemokine, CXCL13, play in tumor immunity across multiple tumor types. Both B cells and CXCL13 possess dualistic impacts on tumor progression and tumor immunity which is furthered detail in this review. Specifically, various B cells subtypes are able to suppress or enhance several important immunological functions. Paradoxically, CXCL13 has been shown to drive several pro-growth and invasive signaling pathways across multiple tumor types, while also, correlating with improved survival and immune cell tumor localization in other tumor types. Potential tools for better elucidating the mechanisms by which B cells and CXCL13 impact the antitumor immune response are also discussed. In addition, multiples strategies are proposed for modulating the B cell-CXCL13 axis for cancer immunotherapies.

Indexed as

AnimalsB-LymphocytesChemokine CXCL13HumansImmunotherapyNeoplasm ProteinsNeoplasmsTumor MicroenvironmentChemokine CXCL13CXCL13 protein, humanNeoplasm ProteinsB cellCXCL13tumor immune cell interactiontumor immunologytumor infiltrated immune cells

Identifiers

PMID33193299
PMCPMC7609404
OpenAlexW3094090913

What OpenQuestion holds

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LicenceCC BY
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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.