Significant association between clinical characteristics and immuno-phenotypes in patients with ANCA-associated vasculitis

Author:

Matsumoto Kotaro1ORCID,Suzuki Katsuya1,Yoshimoto Keiko12,Seki Noriyasu3,Tsujimoto Hideto3,Chiba Kenji3,Takeuchi Tsutomu1

Affiliation:

1. Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan

2. Clinical and Translational Research Center, Keio University Hospital, Tokyo, Japan

3. Mitsubishi Tanabe Pharma Corporation, Kouhoku-ku, Yokohama, Kanagawa, Japan

Abstract

AbstractObjectivesTo elucidate the association between clinical characteristics and immuno-phenotypes in patients with ANCA-associated vasculitis (AAV).MethodsPeripheral blood from 36 patients with active AAV and 18 healthy controls was examined for numbers of circulating T cells, B cells, NK cells, dendritic cells, monocytes and granulocytes using flow cytometry. These immuno-phenotyping data were subjected to cluster analysis and principal components analysis to divide AAV patients into subgroups. Associated organ involvement or therapeutic prognosis were assessed for each subgroup.ResultsAAV patients had higher proportions of plasma cells, plasmablasts, activated T cells, CD14++ CD16+ monocytes, eosinophils and neutrophils than healthy controls. Immuno-phenotyping findings were similar between patients with microscopic polyangiitis, granulomatosis with polyangiitis and eosinophilic granulomatosis with polyangiitis. Cluster analysis indicated that AAV patients could be divided into three subgroups according to peripheral immune cell numbers: antibody production-related (n = 9), cytotoxic activity-related (n = 4) and neutrocytosis/lymphocytopenia-related (n = 23). The antibody production-related or cytotoxic activity-related group was associated with CNS involvement, and the neutrocytosis/lymphocytopenia-related group was associated with high incidence of kidney involvement. Incidence of severe infection was markedly higher in the neutrocytosis/lymphocytopenia-related group than the other two groups. Incidence of disease relapse was comparable among the three groups.ConclusionPatients with active AAV can be divided into three subgroups based on immuno-phenotyping. These results may provide a hint to understanding disease pathophysiology and prognosis, and determining appropriate treatment.

Funder

Mitsubishi Tanabe Pharma Corporation

Keio University School of Medicine

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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