Haifeng M. Wu
Ohio State University
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Publication
Featured researches published by Haifeng M. Wu.
British Journal of Haematology | 2007
Spero R. Cataland; Ming Jin; Amy K. Ferketich; Melanie S. Kennedy; Eric H. Kraut; James N. George; Haifeng M. Wu
We present the results of two consecutively performed cohort studies that evaluated the clinical effects of corticosteroids or ciclosporin as an adjunct to plasma exchange (PE) for the treatment of an acute episode of thrombotic thrombocytopenic purpura (TTP). In comparing 12 corticosteroid‐treated patients with eight ciclosporin‐treated patients, none of the ciclosporin‐treated patients suffered an exacerbation or recurrence of TTP in the first 30u2003d after discontinuing PE compared with 6/10 (60%) of the corticosteroid‐treated patients (Pu2003=u20030·042). These data suggest that ciclosporin may have advantages over corticosteroids as an adjunct to PE therapy in the initial treatment of idiopathic TTP.
Proteome Science | 2006
Ming Jin; Philip T. Diaz; Tran Bourgeois; Charis Eng; Clay B. Marsh; Haifeng M. Wu
Background:Blood monocytes play a central role in regulating host inflammatory processes through chemotaxis, phagocytosis, and cytokine production. However, the molecular details underlying these diverse functions are not completely understood. Understanding the proteomes of blood monocytes will provide new insights into their biological role in health and diseases.Results:In this study, monocytes were isolated from five healthy donors. Whole monocyte lysates from each donor were then analyzed by 2D gel electrophoresis, and proteins were detected using Sypro Ruby fluorescence and then examined for phosphoproteomes using ProQ phospho-protein fluorescence dye. Between 1525 and 1769 protein spots on each 2D gel were matched, analyzed, and quantified. Abundant protein spots were then subjected to analysis by mass spectrometry. This report describes the protein identities of 231 monocyte protein spots, which represent 164 distinct proteins and their respective isoforms or subunits. Some of these proteins had not been previously characterized at the protein level in monocytes. Among the 231 protein spots, 19 proteins revealed distinct modification by protein phosphorylation.Conclusion:The results of this study offer the most detailed monocyte proteomic database to date and provide new perspectives into the study of monocyte biology.
Scientifica | 2014
Shiva Rahmanian; Karen L. Wood; Shili Lin; Mark A. King; April Horne; Shangbin Yang; Haifeng M. Wu; Philip T. Diaz
Background. HIV-infected subjects have an increased incidence of pulmonary emphysema. There are known gender differences in COPD phenotypic expression and diagnosis, but this is not well characterized in lung disease related to HIV. We analyzed a group at risk for the development of COPD (HIV-infected smokers) to determine gender differences in pulmonary symptoms, pulmonary function tests, and HRCT appearances. Methods. This was a cross-sectional, baseline analysis of a prospective study performed between 2006 and 2010. We performed symptomatic, pulmonary function, and computed tomography assessments in 243 HIV-infected smokers. In a subset bronchoalveolar lavage was performed with proteomic analysis of their alveolar macrophages. Results. The majority of the participants were male 213 (87.6%). There was significantly higher percentage of cough and phlegm production in males. There was also a lower FEV1 and a higher RV in males than females. Proteomic analysis revealed 29 proteins with at least a 2-fold higher expression in males and 13 identified proteins that were higher in females. Conclusions. In this group of HIV-infected smokers, airway symptoms and pulmonary function test abnormalities were higher in men than women. These gender differences may be due to differential expression of certain proteins in this group.
Proteomics | 2005
Ming Jin; Garry Drwal; Tran Bourgeois; Joel H. Saltz; Haifeng M. Wu
American Journal of Respiratory Cell and Molecular Biology | 2004
Ming Jin; Judy M. Opalek; Clay B. Marsh; Haifeng M. Wu
American Journal of Physiology-lung Cellular and Molecular Physiology | 2005
Haifeng M. Wu; Ming Jin; Clay B. Marsh
Blood | 2005
Spero R. Cataland; Ming Jin; Amy K. Ferketich; Eric H. Kraut; James N. George; Haifeng M. Wu
Blood | 2004
Spero R. Cataland; James N. George; Eric H. Kraut; Tran T. Bourgeois; Amy K. Ferketich; Melanie S. Kennedy; Michael A. Caligiuri; Haifeng M. Wu
Personalized Medicine | 2010
Haifeng M. Wu; LiHui Xu; Daniel D Sedmak; Clay B. Marsh; Mark W Wurster
Blood | 2007
Spero R. Cataland; Ming Jin; Shili Lin; Melanie S. Kennedy; Eric H. Kraut; James N. George; Haifeng M. Wu