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Increased numbers of CD23+CD21hi Bin-like B cells in human reactive and rheumatoid arthritis lymph nodes

Identifieur interne : 000F71 ( Main/Exploration ); précédent : 000F70; suivant : 000F72

Increased numbers of CD23+CD21hi Bin-like B cells in human reactive and rheumatoid arthritis lymph nodes

Auteurs : Igor I. Kuzin [États-Unis] ; Stephen L. Kates [États-Unis] ; Yawen Ju [États-Unis] ; Longze Zhang [États-Unis] ; Homaira Rahimi [États-Unis] ; Wojciech Wojciechowski [États-Unis] ; Steven H. Bernstein [États-Unis] ; Richard Burack [États-Unis] ; Edward M. Schwarz [États-Unis] ; Andrea Bottaro [États-Unis]

Source :

RBID : PMC:4942352

Abstract

A unique population of CD23+ CD21highB cells in inflamed nodes (Bin) has been shown to accumulate in lymph nodes (LNs) draining inflamed joints of TNF-transgenic (TNF-tg) mice. Bin cells contribute to arthritis flare in mice by distorting node architecture and hampering lymphatic flow, but their existence in human inflamed LNs has not yet been described. Here, we report the characterization of resident B-cell populations in fresh popliteal lymph nodes (PLNs) from patients with severe lower limb diseases (non-RA) and rheumatoid arthritis (RA) patients, and from banked, cryopreserved reactive and normal human LN single cell suspension samples. Bin-like B cells were shown to be significantly increased in reactive LNs, and strikingly elevated (>30% of total) in RA samples. Histopathology and immunofluorescence analyses were consistent with B follicular hyperplasia and histological alterations in RA vs. non-RA PLNs. This is the first description of Bin-like B cells in human inflamed LNs. Consistent with published mouse data, this population appears to be associated with inflammatory arthritis and distortion of LN architecture. Further analyses are necessary to assess the role of CD23+CD21hi Bin-like B cells in RA pathogenesis and arthritic flare.


Url:
DOI: 10.1002/eji.201546266
PubMed: 27105894
PubMed Central: 4942352


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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Bin-like B cells in human reactive and rheumatoid arthritis lymph nodes</title>
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<name sortKey="Wojciechowski, Wojciech" sort="Wojciechowski, Wojciech" uniqKey="Wojciechowski W" first="Wojciech" last="Wojciechowski">Wojciech Wojciechowski</name>
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<p id="P2">A unique population of CD23
<sup>+</sup>
CD21
<sup>high</sup>
<underline>B</underline>
cells in inflamed
<underline>n</underline>
odes (Bin) has been shown to accumulate in lymph nodes (LNs) draining inflamed joints of TNF-transgenic (TNF-tg) mice. Bin cells contribute to arthritis flare in mice by distorting node architecture and hampering lymphatic flow, but their existence in human inflamed LNs has not yet been described. Here, we report the characterization of resident B-cell populations in fresh popliteal lymph nodes (PLNs) from patients with severe lower limb diseases (non-RA) and rheumatoid arthritis (RA) patients, and from banked, cryopreserved reactive and normal human LN single cell suspension samples. Bin-like B cells were shown to be significantly increased in reactive LNs, and strikingly elevated (>30% of total) in RA samples. Histopathology and immunofluorescence analyses were consistent with B follicular hyperplasia and histological alterations in RA vs. non-RA PLNs. This is the first description of Bin-like B cells in human inflamed LNs. Consistent with published mouse data, this population appears to be associated with inflammatory arthritis and distortion of LN architecture. Further analyses are necessary to assess the role of CD23
<sup>+</sup>
CD21
<sup>hi</sup>
Bin-like B cells in RA pathogenesis and arthritic flare.</p>
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<name sortKey="Wojciechowski, Wojciech" sort="Wojciechowski, Wojciech" uniqKey="Wojciechowski W" first="Wojciech" last="Wojciechowski">Wojciech Wojciechowski</name>
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