Literature DB >> 36074221

Clinical value of plasmablasts in predicting disease relapse in patients with IgG4-related disease.

Yiwen Wang1, Zheng Zhao1, Dai Gao1, Hui Wang1, Simin Liao1, Gui Luo1, Xiaojian Ji1, Yan Li1, Xiuru Wang1, Yurong Zhao1, Kunpeng Li1, Jie Zhang1, Jingyu Jin1, Yamei Zhang1, Jian Zhu2, Jianglin Zhang1, Feng Huang3.   

Abstract

OBJECTIVES: To explore the value of plasmablasts in predicting disease relapse in IgG4-related diseases (IgG4-RD).
METHODS: Treatment-naïve IgG4-RD patients treated with glucocorticoid (GC) monotherapy or leflunomide (LEF) and GC combination therapy diagnosed at the Chinese PLA General Hospital during February 2017 and January 2018 were included in this study. The absolute plasmablast count was measured by using the absolute count tubes with flow cytometry. Patients were categorized into high and low plasmablast level groups by defining the median number of plasmablasts as the cut-off value. The characteristics of the clinical manifestations between the two groups were compared. In addition, the correlation of plasmablast count with other indicators and its clinical value in predicting disease relapse were evaluated.
RESULTS: Data of 37 treatment-naïve IgG4-RD patients were analyzed. The median (IQR) absolute count of plasmablasts was 4.0 (2.8-7.5)/μL, which was correlated with the lymphocyte percentage, serum IgG, IgG4, and IgG4/IgG. The baseline absolute count of plasmablasts was an independent risk factor for disease relapse in IgG4-RD patients (HR, 1.199; 95% CI, 1.030-1.396, P = 0.019), and the application of LEF was an independent protective factor (HR, 0.283; 95% CI, 0.106-0.759, p = 0.012).
CONCLUSIONS: The present study preliminarily indicated that baseline absolute plasmablast count may independently predict disease relapse in patients with IgG4-RD treated with GC monotherapy or LEF and GC combination therapy. More efforts are still needed to be performed in the future. Key Points • The absolute count of plasmablasts is correlated with the lymphocyte percentage, serum IgG, IgG4 and IgG4/IgG. • The baseline absolute plasmablast count may predict disease relapse in patients with IgG4-RD treated with GC monotherapy or LEF and GC combination therapy. • The application of LEF is an independent protective factor for disease relapse in IgG4-RD.
© 2022. The Author(s), under exclusive licence to International League of Associations for Rheumatology (ILAR).

Entities:  

Keywords:  Biomarker; Disease relapse; Glucocorticoids; IgG4-related disease; Immunosuppressive agents; Leflunomide; Plasmablasts

Year:  2022        PMID: 36074221     DOI: 10.1007/s10067-022-06339-0

Source DB:  PubMed          Journal:  Clin Rheumatol        ISSN: 0770-3198            Impact factor:   3.650


  14 in total

Review 1.  IgG4-related disease: an update on pathophysiology and implications for clinical care.

Authors:  Cory A Perugino; John H Stone
Journal:  Nat Rev Rheumatol       Date:  2020-09-16       Impact factor: 20.543

Review 2.  Immune mechanisms of fibrosis and inflammation in IgG4-related disease.

Authors:  Shiv Pillai; Cory Perugino; Naoki Kaneko
Journal:  Curr Opin Rheumatol       Date:  2020-03       Impact factor: 5.006

3.  Circulating Th2 memory cells in IgG4-related disease are restricted to a defined subset of subjects with atopy.

Authors:  H Mattoo; E Della-Torre; V S Mahajan; J H Stone; S Pillai
Journal:  Allergy       Date:  2013-12-31       Impact factor: 13.146

Review 4.  Clonally expanded cytotoxic CD4+ T cells and the pathogenesis of IgG4-related disease.

Authors:  Hamid Mattoo; John H Stone; Shiv Pillai
Journal:  Autoimmunity       Date:  2017-02       Impact factor: 2.815

5.  Number of Circulating Follicular Helper 2 T Cells Correlates With IgG4 and Interleukin-4 Levels and Plasmablast Numbers in IgG4-Related Disease.

Authors:  Mitsuhiro Akiyama; Katsuya Suzuki; Kunihiro Yamaoka; Hidekata Yasuoka; Masaru Takeshita; Yuko Kaneko; Harumi Kondo; Yoshiaki Kassai; Takahiro Miyazaki; Rimpei Morita; Akihiko Yoshimura; Tsutomu Takeuchi
Journal:  Arthritis Rheumatol       Date:  2015-09       Impact factor: 10.995

6.  B lymphocytes directly contribute to tissue fibrosis in patients with IgG4-related disease.

Authors:  Emanuel Della-Torre; Elena Rigamonti; Cory Perugino; Simona Baghai-Sain; Na Sun; Naoki Kaneko; Takashi Maehara; Lucrezia Rovati; Maurilio Ponzoni; Raffaella Milani; Marco Lanzillotta; Vinay Mahajan; Hamid Mattoo; Ivan Molineris; Vikram Deshpande; John H Stone; Massimo Falconi; Angelo A Manfredi; Shiv Pillai
Journal:  J Allergy Clin Immunol       Date:  2019-07-15       Impact factor: 10.793

7.  Plasmablasts as a biomarker for IgG4-related disease, independent of serum IgG4 concentrations.

Authors:  Zachary S Wallace; Hamid Mattoo; Mollie Carruthers; Vinay S Mahajan; Emanuel Della Torre; Hang Lee; Maria Kulikova; Vikram Deshpande; Shiv Pillai; John H Stone
Journal:  Ann Rheum Dis       Date:  2014-05-09       Impact factor: 19.103

8.  De novo oligoclonal expansions of circulating plasmablasts in active and relapsing IgG4-related disease.

Authors:  Hamid Mattoo; Vinay S Mahajan; Emanuel Della-Torre; Yurie Sekigami; Mollie Carruthers; Zachary S Wallace; Vikram Deshpande; John H Stone; Shiv Pillai
Journal:  J Allergy Clin Immunol       Date:  2014-05-06       Impact factor: 10.793

9.  Clonal expansion of CD4(+) cytotoxic T lymphocytes in patients with IgG4-related disease.

Authors:  Hamid Mattoo; Vinay S Mahajan; Takashi Maehara; Vikram Deshpande; Emanuel Della-Torre; Zachary S Wallace; Maria Kulikova; Jefte M Drijvers; Joe Daccache; Mollie N Carruthers; Flavia V Castelino; James R Stone; John H Stone; Shiv Pillai
Journal:  J Allergy Clin Immunol       Date:  2016-03-11       Impact factor: 10.793

10.  Development of an IgG4-RD Responder Index.

Authors:  Mollie N Carruthers; John H Stone; Vikram Deshpande; Arezou Khosroshahi
Journal:  Int J Rheumatol       Date:  2012-04-24
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