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Immunological Investigations
A Journal of Molecular and Cellular Immunology
Volume 49, 2020 - Issue 1-2
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Original Articles

Increased Non-switched Memory B Cells are Associated with Plasmablasts, Serum IL-6 Levels and Renal Functional Impairments in IgAN Patients

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Pages 178-190 | Published online: 31 Oct 2019
 

ABSTRACT

Background: Circulating B cells are crucial for the pathogenesis of IgA nephropathy (IgAN). This study aimed at investigating the relationship between frequency of different subsets of circulating B cells and clinical measures in IgAN patients.

Methods: The percentages of different subsets of circulating B cells in 23 IgAN patients and 14 healthy controls (HC) were determined by flow cytometry. Their serum IL-6 levels were measured by Cytometric Bead Array (CBA). Clinical parameters in five patients were measured before and after treatment for 8–12 weeks. The potential relationship between variants was analyzed.

Results: In comparison with the HC, the frequency of CD3-CD19+ CD27+ IgD+IgM+ non-switched memory B cells (P = .0038) and CD3-CD19+ CD27hiCD38hi plasmablasts (P = .0467) and serum IL-6 (P = .0392) levels significantly increased in IgAN patients. The percentages of non-switched memory B cells were positively correlated with plasmablasts (R = 0.5781, P = .0039) and serum IL-6 levels (R = 0.6663, P = .0005) in the patients. The percentages of non-switched memory B cells (R = 0.8399, P < .0001), plasmablasts (R = 0.4486, P = .0318) and the levels of serum IL-6 (R = 0.5461, P = .0070) were positively correlated with the values of 24-h urine proteins in IgAN patients. The serum levels of IL-6 were negatively correlated with the eGFR values. Following standard treatment, the frequency of non-switched memory B cells and plasmablasts and the levels of 24-h urine proteins (P = .0317, P = .0079, P < .05) significantly decreased in IgAN patients.

Conclusions: Abnormally higher frequency of non-switched memory B cells and plasmablasts may contribute to the pathogenesis of IgAN and be potential biomarkers for IgAN.

Additional information

Funding

This work was supported by grants from theNationalNatural Science Foundation of China [No. 30972610,81273240, 91742107 and 81570002], National key research and development program [No.2017YFC0910000 and 2017YFD0501300], Jilin Province Science and Technology Agency [No.20190101022JH, 20160101037JC, 20170622009JC, 2017C021, 2017J039, SXGJXX2017-8,JJKH20180197KJ, DBXM154-2018, 2018SCZWSZX-015], the fund of the State Key Laboratory of Kidney Diseases in PLA General Hospital[No.KF-01-147].

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