PMID- 19379153 OWN - NLM STAT- MEDLINE DCOM- 20090716 LR - 20090421 IS - 1744-9987 (Electronic) IS - 1744-9979 (Linking) VI - 13 IP - 2 DP - 2009 Apr TI - Granulocyte and monocyte adsorption apheresis therapy modulates monocyte-derived dendritic cell function in patients with ulcerative colitis. PG - 138-46 LID - 10.1111/j.1744-9987.2009.00668.x [doi] AB - The aim of this study was to elucidate the molecular mechanisms responsible for the therapeutic effects of granulocyte and monocyte adsorption apheresis (GMA). We investigated the alterations in circulating monocyte subsets and monocyte-derived dendritic cell (moDC) function after GMA therapy in ulcerative colitis (UC) patients. Eighteen patients with UC were enrolled: 14 patients were responders, and 4 patients were non-responders. Peripheral venous blood was obtained within 5 min before and 5 min after GMA therapy. Flow cytometric analysis for monocyte markers (CD14/CD16) was then performed. Monocyte-derived dendritic cells were obtained and alterations in their phenotype were analyzed by flow cytometry. Their function was also analyzed in a mixed lymphocyte reaction assay between allo-naive T lymphocytes. Flow cytometric analysis for intracellular interferon (IFN)-gamma (T-helper 1 cells) and interleukin (IL)-4 (T-helper 2 cells) was then performed for the stimulated T lymphocytes. In patients who responded to GMA, the average numbers of monocytes, especially CD16(+) monocytes, were significantly decreased after therapy (P < 0.05). In responders, post-GMA moDCs expressed significantly lower CD80 and B7-DC, which are one of the stimulation and maturation markers of dendritic cells, compared to pre-GMA moDCs. CD83, CD86 and human leukocyte antigen-DR also showed a tendency to decrease. In responders, naive T lymphocytes stimulated with post-GMA moDCs produced significantly less IFN-gamma and IL-4 compared to those stimulated with pre-GMA moDCs. The results of our study show that some of the immunosuppressive effects of GMA therapy may be associated with the modulation of monocyte subsets and moDC function. FAU - Iwakami, Yuko AU - Iwakami Y AD - Division of Gastroenterology and Hepatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan. FAU - Sakuraba, Atsushi AU - Sakuraba A FAU - Sato, Toshiro AU - Sato T FAU - Takada, Yasuhiro AU - Takada Y FAU - Izumiya, Motoko AU - Izumiya M FAU - Ichikawa, Hitoshi AU - Ichikawa H FAU - Hibi, Toshifumi AU - Hibi T LA - eng PT - Clinical Trial PT - Journal Article PL - Australia TA - Ther Apher Dial JT - Therapeutic apheresis and dialysis : official peer-reviewed journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy JID - 101181252 RN - 207137-56-2 (Interleukin-4) RN - 82115-62-6 (Interferon-gamma) SB - IM MH - Adult MH - Aged MH - Blood Component Removal/*methods MH - Colitis, Ulcerative/blood/*therapy MH - Dendritic Cells/metabolism MH - Female MH - Flow Cytometry MH - Granulocytes/*metabolism MH - Humans MH - Interferon-gamma/metabolism MH - Interleukin-4/metabolism MH - Male MH - Middle Aged MH - Monocytes/*metabolism MH - Phenotype MH - T-Lymphocytes/metabolism MH - Treatment Outcome MH - Young Adult EDAT- 2009/04/22 09:00 MHDA- 2009/07/17 09:00 CRDT- 2009/04/22 09:00 PHST- 2009/04/22 09:00 [entrez] PHST- 2009/04/22 09:00 [pubmed] PHST- 2009/07/17 09:00 [medline] AID - TAP668 [pii] AID - 10.1111/j.1744-9987.2009.00668.x [doi] PST - ppublish SO - Ther Apher Dial. 2009 Apr;13(2):138-46. doi: 10.1111/j.1744-9987.2009.00668.x.