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Chronic Obstructive Pulmonary Disease (COPD): Evaluation From Clinical, Immunological and Bacterial Pathogenesis Perspectives

期刊

JOURNAL OF MICROBIOLOGY
卷 52, 期 3, 页码 211-226

出版社

MICROBIOLOGICAL SOCIETY KOREA
DOI: 10.1007/s12275-014-4068-2

关键词

Chronic obstructive pulmonary disease (COPD); smoking; innate and adaptive immunity; airway infections; Pseudomonas aeruginosa; biofilm

资金

  1. Department of Veteran's Affair, Cincinnati OH VA Hospital
  2. National Institutes of Health [R01 ES015036, R21 HL109635]
  3. Flight Attendant Medical Research Institute

向作者/读者索取更多资源

Chronic obstructive pulmonary disease (COPD), a disease manifested by significantly impaired airflow, afflicts similar to 14.2 million cases in the United States alone with an estimated 63 million people world-wide. Although there are a number of causes, the predominant cause is excessive tobacco smoke. In fact, in China, there have been estimates of 315,000,000 people that smoke. Other less frequent causes are associated with indirect cigarette smoke, air pollutants, biomass fuels, and genetic mutations. COPD is often associated with heart disease, lung cancer, osteoporosis and conditions can worsen in patients with sudden falls. COPD also affects both innate and adaptive immune processes. Cigarette smoke increases the expression of matrix metalloproteases and proinflammatory chemokines and increases lung titers of natural killer cells and neutrophils. Yet, neutrophil reactive oxygen species (ROS) mediated by the phagocytic respiratory burst and phagocytosis is impaired by nicotine. In contrast to innate immunity in COPD, dendritic cells represent leukocytes recruited to the lung that link the innate immune responses to adaptive immune responses by activating naive T cells through antigen presentation. The autoimmune process that is also a significant part of inflammation associated with COPD. Moreover, coupled with restricted FEV1 values, are the prevalence of patients with single or multiple infections by bacteria, viruses and fungi. Finally, we focus on one of the more problematic infectious agents, the Gram-negative opportunistic pathogenic bacterium, Pseudomonas aeruginosa. Specifically, we delve into the development of highly problematic biofilm infections that are highly refractory to conventional antibiotic therapies in COPD. We offer a nonconventional, biocidal treatment that may be effective for COPD airway infections as well as with combinations of current antibiotic regimens for more effective treatment outcomes and relief for patients with COPD.

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