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Association of reactive oxygen and nitrogen intermediate and complement levels with apoptosis of peripheral blood mononuclear cells in lupus patients.

Association of reactive oxygen and nitrogen intermediate and complement levels with apoptosis of peripheral blood mononuclear cells in lupus patients. Research Abstract Details 

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  • Association of reactive oxygen and nitrogen intermediate and complement levels with apoptosis of peripheral blood mononuclear cells in lupus patients. Abstract Text:

    james c oatesJames C Oates,libby w farrellyLibby W Farrelly,ann f hofbauerAnn F Hofbauer,wei wangWei Wang,gary s gilkesonGary S Gilkeson,james c oatesJames C Oates,libby w farrellyLibby W Farrelly,ann f hofbauerAnn F Hofbauer,wei wangWei Wang,gary s gilkesonGary S Gilkeson,

    OBJECTIVE: Both increased production of reactive oxygen and nitrogen intermediates (RONI) and reduced levels of complement may play a role in the increased apoptosis and reduced clearance of apoptotic cells in systemic lupus erythematosus (SLE). The objective of this study was to evaluate both processes in a parallel, prospective, longitudinal manner. METHODS: Sixty-seven SLE patients were evaluated during multiple visits, and 31 healthy control subjects were evaluated once or twice. Clinical and laboratory features of SLE disease activity were determined, and blood was collected for measurement of serum nitrate plus nitrite (NOx) levels and for isolation of peripheral blood mononuclear cells (PBMCs). PBMCs were cultured with a nitric oxide (NO) donor and SLE or control plasma, with or without heat inactivation, cobra venom factor (CVF), or lipopolysaccharide plus interferon-gamma treatment. Cells were analyzed for apoptotic index (AI), cellular subsets, and RONI production. RESULTS: The PBMC AI was associated with SLE and was inversely associated with complement levels over time. Changes in the AI with addition of a NO donor was longitudinally associated with serum NOx levels, and stimulation of SLE PBMCs led to parallel increases in RONI production and apoptosis. Addition of SLE plasma resulted in a greater PBMC AI, an effect that was increased with heat inactivation and was corrected with CVF treatment. CONCLUSION: These data suggest that the greater AI observed in SLE PBMCs relates to increased PBMC RONI production and reduced complement levels. The longitudinal nature of these parallel associations within individuals suggests that these processes are dynamic and additive.

    Association of reactive oxygen and nitrogen intermediate and complement levels with apoptosis of peripheral blood mononuclear cells in lupus patients. Publishing Authors By Initials

    jc oatesJC Oates,lw farrellyLW Farrelly,af hofbauerAF Hofbauer,w wangW Wang,gs gilkesonGS Gilkeson,jc oatesJC Oates,lw farrellyLW Farrelly,af hofbauerAF Hofbauer,w wangW Wang,gs gilkesonGS Gilkeson,

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    Association of reactive oxygen and nitrogen intermediate and complement levels with apoptosis of peripheral blood mononuclear cells in lupus patients. Journal Published:

    PUBLICATION TYPE: Research Support, U.S. Gov't,

    Journal: Arthritis and rheumatism

    VOLUME: 56

    Page Numbers: 3738-47

    Journal Abbreviation: Arthritis Rheum.

    ISSN: 0004-3591

    DAY: 26

    MONTH: Nov

    YEAR: 2007

    Association of reactive oxygen and nitrogen intermediate and complement levels with apoptosis of peripheral blood mononuclear cells in lupus patients. Information

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    LANGUAGE: eng

    NlmUniqueID: 370605

    Association of reactive oxygen and nitrogen intermediate and complement levels with apoptosis of peripheral blood mononuclear cells in lupus patients. Keywords Mesh Terms:

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    Grant and Affiliation Information for Association of reactive oxygen and nitrogen intermediate and complement levels with apoptosis of peripheral blood mononuclear cells in lupus patients.

    AFFILIATION: Medical University of South Carolina, Department of Medicine, Division of Rheumatology, Charleston, SC 29425, USA. oatesjc@musc.edu

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NCRR

    GRANT: M01-RR-01070

    ACRONYM: RR

    MEDLINETA: Arthritis Rheum

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