Instead, we found lower levels of CD16+ cells in the pool of mono

Instead, we found lower levels of CD16+ cells in the pool of monocytes in our APS I cohort. CD16, also termed ‘FcγRIII’, is a member of the Fc-receptor family (for review, see [46]). This receptor is specific for binding small IgG complexes, which should be constantly forming in APS I as they have high titres of a plethora of autoantibodies. Crosslinking CD16 can induce production of TNFα and IL1β in monocytes. It has been reported that CD16+ monocytes and CD16− monocytes have the same capability of

differentiating into DC, but the expression of specific DC markers like CD86, CD11a and CD11c and their potential to secrete IL-4 and proinflammatory cytokines differ [31, 32]. The downregulation of CD16 on APS I monocytes could be a result of massive immune complex binding to the receptor followed by internalization. Our studies CP-868596 purchase showed contradictory results for many immune cell subpopulations compared with earlier reports. Several of the cellular abnormalities described here or previously are most probably not the result of thymic malfunction but the reflection of longstanding autoimmunity and inflammation caused by C. albicans infection. As the study groups cannot be large because of the rarity of the disease, the results of immunophenotyping

may depend on the duration and activity Alectinib purchase of the disease components in studied patients. In conclusion, we here report the most comprehensive immunophenotypic study which has been published on patients with APS I and relatives. Our data suggest that patients with APS I have disturbances in the Treg compartment, less CCR6+CXCR3+ Th cells and http://www.selleck.co.jp/products/cobimetinib-gdc-0973-rg7420.html less CD16+ monocytes, which may explain their propensity for autoimmune manifestations. We will express our gratitude to the patients, relatives and healthy controls for donating blood samples for the study. The doctors Kristian Fougner, Jens Bollerslev, Kristian Løvås

and Bjørn Nedrebø are thanked for recruiting patients to the study. We will furthermore thank Hajirah Muneer, Institute of Medicine, University of Bergen, for excellent technical skills in the handling of cell samples. The study was supported by grants from Helse Vest and the European Regional Fund and Archimedes Foundation and Estonian Science Foundation grant 8358. Anette Bøe Wolff has been a post-doctoral fellow of the The Research Council of Norway. Table S1 Demographics of APS I families included in the immunophenotypic studies. Table S2 Immunophenotyping of APS I patients, relatives and healthy controls. Please note: Wiley-Blackwell are not responsible for the content or functionality of any supporting materials supplied by the authors. Any queries (other than missing material) should be directed to the corresponding author for the article.

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