Evidence map›Paper›PMID 28894445›Full record

ReviewFrontiers in immunology2017

Adipose Tissue Inflammation Induces B Cell Inflammation and Decreases B Cell Function in Aging.

Daniela Frasca, Bonnie B Blomberg

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

42 citing papers in PubMed, 67 citations in OpenAlex.

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  13. The 'omics of obesity in B-cell acute lymphoblastic leukemia.Journal of the National Cancer Institute. Monographs · 2023
    Article
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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

2 authors at 1 institution in 1 country.

Daniela FrascaDepartment of Microbiology and Immunology, University of Miami Miller School of Medicine, Miami, FL, United States.
Bonnie B BlombergDepartment of Microbiology and Immunology, University of Miami Miller School of Medicine, Miami, FL, United States.
University of Miami · US

Funding

Regulation of Immunoglobulin Class Switch in Aged MiceR37AG023717 · NIA · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI BLOMBERG, BONNIE B. · 2005 to 2014
$3.3M
How do obesity and related inflammation decrease antibody responses in aging?R01AG023717 · NIA · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI BLOMBERG, BONNIE B., FRASCA, DANIELA · 2017 to 2021
$1.8M
Regulation of B Lymphocyte Defects in Senescent HumansR01AG032576 · NIA · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI BLOMBERG, BONNIE B. · 2009 to 2014
$1.6M
Regulation of primary and memory B cell vaccine responses in the elderlyR56AG032576 · NIA · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI BLOMBERG, BONNIE B., FRASCA, DANIELA · 2015 to 2015
$598k
Micro-RNAs: a new mechanism negatively regulating B cell responses in the elderlyR21AG042826 · NIA · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI BLOMBERG, BONNIE B., FRASCA, DANIELA · 2013 to 2014
$422k
Molecular mechanisms for TNF-mediated inhibition of B lymphocyte functionR21AI096446 · NIAID · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI BLOMBERG, BONNIE B., FRASCA, DANIELA · 2012 to 2013
$407k
NIAID NIH HHS R21 AI096446NIA NIH HHS R01 AG023717NIA NIH HHS R01 AG032576NIA NIH HHS R21 AG042826NIA NIH HHS R37 AG023717NIA NIH HHS R56 AG032576
6 · The paper itself

Abstract

Aging is the greatest risk factor for developing chronic diseases. Inflamm-aging, the age-related increase in low-grade chronic inflammation, may be a common link in age-related diseases. This review summarizes recent published data on potential cellular and molecular mechanisms of the age-related increase in inflammation, and how these contribute to decreased humoral immune responses in aged mice and humans. Briefly, we cover how aging and related inflammation decrease antibody responses in mice and humans, and how obesity contributes to the mechanisms for aging through increased inflammation. We also report data in the literature showing adipose tissue infiltration with immune cells and how these cells are recruited and contribute to local and systemic inflammation. We show that several types of immune cells infiltrate the adipose tissue and these include macrophages, neutrophils, NK cells, innate lymphoid cells, eosinophils, T cells, B1, and B2 cells. Our main focus is how the adipose tissue affects immune responses, in particular B cell responses and antibody production. The role of leptin in generating inflammation and decreased B cell responses is also discussed. We report data published by us and by other groups showing that the adipose tissue generates pro-inflammatory B cell subsets which induce pro-inflammatory T cells, promote insulin resistance, and secrete pathogenic autoimmune antibodies.

Indexed as

agingantibody responsesimmunityinflammationobesity

Identifiers

PMID28894445
PMCPMC5581329
OpenAlexW2747063627

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.