Mycobacterium tuberculosis dysregulates MMP/TIMP balance to drive rapid cavitation and unrestrained bacterial proliferation

被引:82
作者
Kuebler, Andre [1 ,2 ]
Luna, Brian [2 ]
Larsson, Christer [3 ]
Ammerman, Nicole C. [4 ]
Andrade, Bruno B. [5 ]
Orandle, Marlene [6 ]
Bock, Kevin W. [6 ]
Xu, Ziyue [7 ]
Bagci, Ulas [7 ]
Molura, Daniel J. [7 ]
Marshall, John [8 ]
Burns, Jay [9 ]
Winglee, Kathryn [2 ]
Ahidjo, Bintou Ahmadou [2 ,12 ]
Cheung, Laurene S. [2 ]
Klunk, Mariah [10 ]
Jain, Sanjay K. [2 ,10 ]
Kumar, Nathella Pavan [13 ,14 ]
Babu, Subash [13 ,15 ]
Sher, Alan [5 ]
Friedland, Jon S. [1 ]
Elkington, Paul T. G. [1 ,11 ]
Bishai, William R. [2 ,12 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, London SW7 2AZ, England
[2] Johns Hopkins Univ, Sch Med, Ctr TB Res, Baltimore, MD USA
[3] Umea Univ, Dept Mol Biol, S-90187 Umea, Sweden
[4] KwaZulu Natal Res Inst TB & HIV K RITH, Durban, South Africa
[5] NIAID, Immunobiol Sect, Parasit Dis Lab, NIH, Bethesda, MD 20892 USA
[6] NIAID, Infect Dis Pathogenesis Sect, Comparat Med Branch, NIH, Bethesda, MD 20892 USA
[7] NIH, Bethesda, MD 20892 USA
[8] Johns Hopkins Sch Med, Baltimore, MD USA
[9] Johns Hopkins Univ, Baltimore, MD USA
[10] Ctr Infect Dis & Inflammat Imaging Res CI3R, Baltimore, MD USA
[11] Univ Southampton, Fac Med, Southampton SO9 5NH, Hants, England
[12] Johns Hopkins Univ, Sch Med, Howard Hughes Med Inst, Baltimore, MD 21205 USA
[13] Int Ctr Excellence Res, Natl Inst Hlth, Madras, Tamil Nadu, India
[14] Natl Inst Res TB, Madras, Tamil Nadu, India
[15] NIAID, Helminth Immunol Sect, Parasit Dis Lab, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
tuberculosis; matrix metalloproteinase; computed tomography; cavity; PULMONARY TUBERCULOSIS; MULTIDRUG-RESISTANT; RABBIT MODEL; T-CELLS; INFECTION; PATHOLOGY; LUNG; MICE; CHALLENGE; VACCINE;
D O I
10.1002/path.4432
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Active tuberculosis (TB) often presents with advanced pulmonary disease, including irreversible lung damage and cavities. Cavitary pathology contributes to antibiotic failure, transmission, morbidity and mortality. Matrix metalloproteinases (MMPs), in particular MMP-1, are implicated in TB pathogenesis. We explored the mechanisms relating MMP/TIMP imbalance to cavity formation in a modified rabbit model of cavitary TB. Our model resulted in consistent progression of consolidation to human-like cavities (100% by day 28), with resultant bacillary burdens (>10(7) CFU/g) far greater than those found in matched granulomatous tissue (10(5) CFU/g). Using a novel, breath-hold computed tomography (CT) scanning and image analysis protocol, we showed that cavities developed rapidly from areas of densely consolidated tissue. Radiological change correlated with a decrease in functional lung tissue, as estimated by changes in lung density during controlled pulmonary expansion (R-2=0.6356, p < 0.0001). We demonstrated that the expression of interstitial collagenase (MMP-1) was specifically greater in cavitary compared to granulomatous lesions (p < 0.01), and that TIMP-3 significantly decreased at the cavity surface. Our findings demonstrated that an MMP-1/TIMP imbalance is associated with the progression of consolidated regions to cavities containing very high bacterial burdens. Our model provided mechanistic insight, correlating with human disease at the pathological, microbiological and molecular levels. It also provided a strategy to investigate therapeutics in the context of complex TB pathology. We used these findings to predict a MMP/TIMP balance in active TB and confirmed this in human plasma, revealing the potential of MMP/TIMP levels as key components of a diagnostic matrix aimed at distinguishing active from latent TB (PPV = 92.9%, 95% CI 66.1-99.8%, NPV = 85.6%; 95% CI 77.0-91.9%). Copyright (c) 2014 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd
引用
收藏
页码:431 / 444
页数:14
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