Evidence map›Paper›PMID 21214915›Full record

ArticleImmunity & ageing : I & A2011

Aging impacts isolated lymphoid follicle development and function.

Keely G McDonald, Matthew R Leach, Conway Huang, Caihong Wang, Rodney D Newberry

Open access · goldAbstract read
In one paragraph

Article in Immunity & ageing : I & A, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

30 citing papers in PubMed, 59 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

5 authors at 2 institutions in 1 country.

Keely G McDonald *Department of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Matthew R Leach *Department of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Conway Huang *University of Texas Southwestern Medical School, Austin Texas, 78701, USA.
Caihong WangDepartment of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Rodney D NewberryDepartment of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Washington University in St. Louis · USThe University of Texas Southwestern Medical Center · US

Funding

Lymphotoxin Beta Receptor in Intestinal InflammationR01DK064798 · NIDDK · WASHINGTON UNIVERSITY · PI NEWBERRY, RODNEY D · 2005 to 2013
$2.8M
NIDDK NIH HHS R01 DK064798
6 · The paper itself

Abstract

backgroundImmunosenescence is the age-related decline and dysfunction of protective immunity leading to a marked increase in the risk of infections, autoimmune disease, and cancer. The majority of studies have focused on immunosenescence in the systemic immune system; information concerning the effect of aging on intestinal immunity is limited. Isolated lymphoid follicles (ILFs) are newly appreciated dynamic intestinal lymphoid structures that arise from nascent lymphoid tissues, or cryptopatches (CP), in response to local inflammatory stimuli. ILFs promote "homeostatic" responses including the production of antigen-specific IgA, thus playing a key role in mucosal immune protection. ILF dysfunction with aging could contribute to immunosenescence of the mucosal system, and accordingly we examined phenotypic and functional aspects of ILFs from young (2 month old) and aged (2 year old) mice.

resultsWe observed that aged mice have increased numbers of ILFs and increased numbers of structures corresponding to an early stage of CPs transforming into ILFs. The cellular composition of ILFs in aged mice is altered with a smaller B-lymphocyte population and an increased T-lymphocyte population. The ILF T-lymphocyte population is notable by the presence of CD4+ CD8αα+ T-lymphocytes, which are absent from the systemic compartment. The smaller B-lymphocyte population in ILFs from aged mice is directly correlated with decreased mRNA and protein expression of CCL20 and CXCL13, two chemokines that play crucial roles in recruiting B-lymphocytes into ILFs. Aged mice had elevated levels of serum and fecal immunoglobulins and despite the decreased B-lymphocyte population, ILFs from aged mice displayed increased IgA production. The immunoglobulin repertoire was skewed in aged mice, and ILFs demonstrated a repertoire usage similar to that of the systemic pool in both young and aged mice.

conclusionsHere we observed that ILF development, cellular composition, and immunoglobulin production are altered with aging suggesting that ILF dysfunction contributes to mucosal immunosenescence.

Identifiers

PMID21214915
PMCPMC3023758
OpenAlexW2145232408

What OpenQuestion holds

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Registered trials

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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.