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      Basophils as a potential marker of lupus nephritis by flow cytometry

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          Abstract

          Objective:

          To establish a convenient and simple flow cytometry immunophenotyping panel to explore immune cellular alterations and potential cellular biomarkers in systemic lupus erythematosus.

          Materials and methods:

          This is a cross-sectional, case–control study including 60 patients with systemic lupus erythematosus and 20 sex- and age-matched healthy controls. A 14-color immunophenotyping panel was applied to detect proportions of circulating immune mononuclear cells, and comparisons between patients and healthy controls, and subgroups of patients, were performed. Correlations between cellular proportions and other parameters were investigated.

          Results:

          After multivariate analysis, significantly decreased proportions of CD4 CD8 T cells, natural killer cells and innate lymphoid cells were observed in patients compared with healthy controls. The proportions of basophils were decreased significantly in patients with lupus nephritis (LN) compared with those in patients without LN.

          Conclusion:

          In the present study, we found that basophil proportions may be a biomarker of LN.

          Lay abstract

          Systemic lupus erythematosus is a chronic, multisystem, autoimmune disorder that involves various abnormalities of immune cells and thus presents in a striking variety of ways. This study aimed to establish a biomarker panel that would enable the exploration of changes in immune cells and the relationships between immune cell subsets and clinical manifestations in patients with systemic lupus erythematosus. Our results showed that basophil cell proportions may be a biomarker of use in lupus nephritis.

          Most cited references37

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          Updating the American college of rheumatology revised criteria for the classification of systemic lupus erythematosus

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            Systemic lupus erythematosus disease activity index 2000.

            To describe the Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2K), a modification of SLEDAI to reflect persistent, active disease in those descriptors that had previously only considered new or recurrent occurrences, and to validate SLEDAI-2K against the original SLEDAI as a predictor for mortality and as a measure of global disease activity in the clinic. All visits in our cohort of 960 patients were used to correlate SLEDAI-2K against the original SLEDAI, and the whole cohort was used to validate SLEDAI-2K as a predictor of mortality. A subgroup of 212 patients with SLE followed at the Lupus Clinic who had 5 regular visits, 3-6 months apart, in 1991-93 was also included. An uninvolved clinician evaluated each patient record and assigned a clinical activity level. The SLEDAI score was calculated from the database according to both the original and modified definitions. SLEDAI-2K correlated highly (r = 0.97) with SLEDAI. Both methods for SLEDAI scoring predicted mortality equally (p = 0.0001), and described similarly the range of disease activity as recognized by the clinician. SLEDAI-2K, which allows for persistent activity in rash, mucous membranes, alopecia, and proteinuria, is suitable for use in clinical trials and studies of prognosis in SLE.
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              Systemic lupus erythematosus.

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                Author and article information

                Journal
                Future Sci OA
                Future Sci OA
                FSOA
                Future Science OA
                Future Science Ltd (London, UK )
                2056-5623
                16 February 2021
                June 2021
                16 February 2021
                : 7
                : 5
                : FSO690
                Affiliations
                [1 ]Department of Rheumatology & Immunology, West China Hospital, Sichuan University, Chengdu, China
                [2 ]Laboratory of Stem Cell Biology, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University & Collaborative Innovation Center for Biotherapy, Chengdu, China
                Author notes
                [* ]Author for correspondence: xmingmoscu@ 123456163.com
                Author information
                https://orcid.org/0000-0002-7713-1696
                https://orcid.org/0000-0001-9932-7457
                Article
                10.2144/fsoa-2020-0212
                8147755
                ba7be8fd-48da-47ce-9a26-07adeacc1055
                © 2021 Xianming Mo

                This work is licensed under the Creative Commons Attribution 4.0 License

                History
                : 19 December 2020
                : 01 February 2021
                : 16 February 2021
                Page count
                Pages: 11
                Categories
                Research Article

                basophils,cd4−cd8− t cells,immunophenotype,innate lymphoid cells,lupus nephritis,systemic lupus erythematosus

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