4.7 Article

Neutrophils Are the Predominant Infected Phagocytic Cells in the Airways of Patients With Active Pulmonary TB

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CHEST
卷 137, 期 1, 页码 122-128

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ELSEVIER SCIENCE BV
DOI: 10.1378/chest.09-0903

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  1. National Institutes of Health, National Institute of Allergy and Infections Diseases [Z01 AI000783-11]
  2. Bill and Melinda Gates Foundation
  3. Wellcome Trust [37882]
  4. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [Z01AI000783, ZIAAI001067] Funding Source: NIH RePORTER

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Background: The exact role of neutrophils in the pathogenesis of TB is poorly understood. Recent evidence suggests that neutrophils are not simply scavenging phagocytes in Mycobacterium tuberculosis (Mtb) infection. Methods: Three different types of clinical specimens from patients with active pulmonary TB who underwent lung surgery were examined: sputum, BAIL fluid, and cavity contents. Differential cell separation and quantification were performed for intracellular and extracellular bacteria, and bacterial length was measured using microscopy. Results: Neutrophils were more abundant than macrophages in sputum (86.6% +/- 2.2% vs 8.4% +/- 1.3%) and in BAL fluid (78.8% +/- 5.8% vs 11.8% +/- 4.1%). Inside the cavity, lymphocytes (41.3% +/- 11.2%) were the most abundant cell type, followed by neutrophils (38.8% +/- 9.4%) and macrophages (19.5% +/- 7.5%). More intracellular bacilli were found in neutrophils than macrophages in sputum (67.6% +/- 5.6% vs 25.2% +/- 6.5%), in BAL fluid (65.1% +/- 14.4% vs 28.3% +/- 11.6%), and in cavities (61.8% +/- 13.3% vs 23.9% +/- 9.3%). The lengths of Mtb were shortest in cavities (1.9 +/- 0.1 mu m), followed by in sputum (2.9 +/- 0.1 mu m) and in BAIL fluid (3.6 +/- 0.2 mu m). Conclusions: Our results show that neutrophils are the predominant cell types infected with AM in patients with TB and that these intracellular bacteria appear to replicate rapidly. These results are consistent with a role for neutrophils in providing a permissive site for a final burst of active replication of the bacilli prior to transmission. CHEST 2010; 137(1):122-128

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