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    題名: Pycnogenol induces differentiation and apoptosis in human promyeloid leukemia HL-60 cells
    作者: Huang, WW;Yang, JS;Lin, CF;Ho, WJ;Lee, MR
    貢獻者: 醫學院醫學系生化學科;China Med Univ, Dept Biochem, Taichung 40403, Taiwan;China Med Univ, Dept Biol, Taichung 404, Taiwan;Yuan Pei Univ Sci & Technol, Dept Med Technol, Hsinchu, Taiwan;Dayeh Univ, Dept Bioresources, Changhua, Taiwan
    日期: 2005
    上傳時間: 2010-09-24 14:55:12 (UTC+8)
    出版者: PERGAMON-ELSEVIER SCIENCE LTD
    摘要: Background and Purpose: Severe acute respirator), syndrome (SARS) is characterized by fever with rapid progression to acute respiratory distress and it is associated with substantial morbidity and mortality. Transmission patterns suggest spread by respiratory droplet or close person-to-person contact. To elucidate the correlation of clinical presentation to the pathogenesis and course of the disease, we reviewed the pulmonary pathologic specimens of SARS patients taken at different stages of the disease. Methods: Four "probable" cases of SARS were studied. SARS-associated coronavirus (SARS-CoV) infection was demonstrated using reverse transcriptase-polymerase chain reaction in all 4 patients. The pulmonary specimens were taken oil day 7 after symptom onset in patient 1, day 11 in patient 2, day 17 in patient 3, and day 21 in patient 4. Results: The autopsy lung tissue from patient 1, who died 7 days after symptoms onset due to the complication of acute myocardial infarction, revealed mild histologic change in the lung. Only focal pulmonary edema or hemorrhage was seen. In the second patient, who (tied I I clays after symptom onset, severe acute alveolar damage was characterized by patchy or diffuse lung edema, hyaline membrane formation, and scarce lymphocytic infiltration. The lymphocytes were mostly CD3-positive and CD20-negative. In the third patient, biopsy specimen taken 17 days after symptom onset showed patches of organizing pneumonia with reactive fibroblastic proliferation, more abundant type 11 pneumocytes and clustering of CD68-positive macrophages within the alveolar spaces. Few CD68-positive syncytial multinucleated giant cells were also seen in the specimens but no viral inclusion body could be identified in these cells. The lung biopsy specimen from patient 4 taken 21 days after symptom onset showed characteristics of the fibrotic stage, with significant myofibroblastic proliferation ill the alveolar space and interstitium resulting in loss of pulmonary architecture. The number of CD3-positive lymphocytes and of CD68-positive macrophages in this specimen from a patient ill the fibrotic phase of diffuse alveolar damage (DAD) whose condition deteriorated was less than in the specimen from case 3 who was in the early proliferative phase of DAD and eventually recovered. Conclusions: The histologic evolution of SARS coincided with the different stages of DAD: acute, proliferative organizing, and fibrotic stages. SARS cannot be differentiated from the other etiologies of DAD by morphologic examination alone. The absence of DAD does not rule Out the possibility of SARS-CoV infection, particularly in the early stage of the disease.
    關聯: LEUKEMIA RESEARCH 29(6):685-692
    顯示於類別:[醫學系] 期刊論文

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