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3 ncoded from detailed interviews of 76 and 64 pulmonary TB patients in the 2 Indian cities of Mumbai a
4 th latent TB infection (LTBI) and 107 active pulmonary TB (APTB) cases, and 24 recently BCG-vaccinate
5 icts/counties (each with at least 300 active pulmonary TB patients registered in 2009) within the pro
7 deep learning system (DLS) to detect active pulmonary TB on chest radiographs and compare its perfor
10 ssed in whole blood can differentiate active pulmonary TB (ATB) from other respiratory diseases (ORDs
11 tegies for evaluating outpatients for active pulmonary TB at the San Francisco Department of Public H
14 uberculosis test for the diagnosis of active pulmonary TB (PTB) with whole blood, plasma, and serum f
15 with symptoms and signs suggestive of active pulmonary TB that were systematically confirmed or ruled
17 5% CI: 86.2 to 100%) for diagnosis of active pulmonary TB when using sputum Xpert MTB/RIF as the refe
20 lt South African cohort (n = 72) with active pulmonary TB (on treatment for 1-4 mo) or pulmonary TB t
21 th symptoms and signs consistent with active pulmonary TB and complete clinical diagnosis were strati
23 curacy of this assay in patients with active pulmonary TB and in control patients with or without lat
24 ensure that contacts of patients with active pulmonary TB are identified and appropriately screened.
25 rom study participants diagnosed with active pulmonary TB in South Africa and compared results to non
28 ne, provides variable efficacy against adult pulmonary TB, but why this protection varies is unclear.
31 Xpert Ultra cartridge for diagnosis of adult pulmonary TB may have different consequences in differen
37 t implications in vaccine strategies against pulmonary TB and other intracellular infections in the l
38 sts could improve diagnosis of both EPTB and pulmonary TB (PTB) and timely initiation of anti-TB ther
39 sts could improve diagnosis of both EPTB and pulmonary TB (PTB), and timely initiation of anti-TB the
40 gene expression signature for both EPTB and pulmonary TB highlighting the translational potential of
41 South Africa, following adults with HIV and pulmonary TB prior to and up to 48 weeks after ART initi
44 sted case-control study on air pollution and pulmonary TB, we observed positive associations with amb
45 re, we present a detailed comparison between pulmonary TB and SARC, including whole-blood gene expres
46 mental findings showed a causal link between pulmonary TB and lung tumorigenesis and established a ge
51 dized patients (SPs) presenting with classic pulmonary TB symptoms were deployed in 3 provinces of Ch
52 proportion of younger patients with clinical pulmonary TB due to NTM and co-infection with HIV and th
55 from adults with bacteriologically confirmed pulmonary TB were also comparable to those reported for
56 rolled adult patients with culture-confirmed pulmonary TB and their close contacts at 9 health depart
58 3/51 (65%) and 33/51 (65%) culture-confirmed pulmonary TB cases, respectively; Xpert MTB/RIF detected
61 cipants: 95 with microbiologically confirmed pulmonary TB (Group 1), 200 household contacts of people
63 we enrolled 3109 microbiologically confirmed pulmonary TB patients and their 12 767 household contact
65 nes in participants with previous or current pulmonary TB may have the potential for causing harmful
69 s associated with reduced risk of developing pulmonary TB but increased risk of rapid progression to
72 e of multi-detector HRCT chest in diagnosing pulmonary TB cases whose sputum smears are negative and
76 ients presenting with a productive cough for pulmonary TB, Xpert blood offers no diagnostic advantage
77 form of TB, are based on those developed for pulmonary TB and not optimized for brain penetration.
80 m a genome-wide association study (GWAS) for pulmonary TB, we found that the response eQTL were more
81 approaches and experimental mouse models for pulmonary TB we characterized MDSCs as novel myeloid pop
84 f sputum (the primary specimen type used for pulmonary TB), careful design and reporting of the speci
91 d 17-69 years; 62% male) diagnosed as having pulmonary TB diseases or non-TB diseases, but who could
93 terise, using RNA sequencing, 44 fresh human pulmonary TB lesion samples from 13 TB individuals (drug
95 nd persistent in a subset of immunocompetent pulmonary TB patients and is characterized by antigen-sp
96 s such as navitoclax can potentially improve pulmonary TB treatments, reduce lung damage / fibrosis a
97 phagosome is a key reservoir of infection in pulmonary TB and multiple studies have shown that inorga
98 lung may affect presentation and outcome in pulmonary TB, and an understanding of the development of
99 of the systemic inflammatory perturbation in pulmonary TB and reveal qualitative changes in inflammat
100 rrow chimeras demonstrate that reductions in pulmonary TB immunopathology are dependent on hematopoie
103 ing might regulate monocyte MMP secretion in pulmonary TB during cell adhesion to the extracellular m
106 Between 2009 and 2012, we recruited incident pulmonary TB patients and their household contacts, whom
107 identified all adults (>15 yr) with incident pulmonary TB (index cases) diagnosed at 106 public healt
109 inflammatory perturbation in treatment-naive pulmonary TB patients and uninfected individuals from In
110 From 1 June 2011 to 7 March 2012, 4,292 new pulmonary TB patients were enrolled across the 36 cluste
111 ed a prospective cohort of patients with new pulmonary TB receiving thrice-weekly treatment in India.
115 ever, from May to September 1997, 3 cases of pulmonary TB were reported among medical waste treatment
116 examine the disease severity in a cohort of pulmonary TB (PTB) individuals with (Ss+) or without (Ss
118 y was performed using records on contacts of pulmonary TB patients at the Public Health Service Amste
121 frequently are not used in the diagnosis of pulmonary TB cases, particularly TB cases with smear-neg
123 ed on adult patients with first diagnosis of pulmonary TB starting treatment in public healthcare fac
126 s or DNA accumulate on the oral epithelia of pulmonary TB patients, and can be collected and detected
127 ociety where TB was prevalent, evaluation of pulmonary TB before prescription of PPI or H2RA is warra
129 personalized medicine for the management of pulmonary TB/cancer particularly for cases that are not
131 In this study, we used a rabbit model of pulmonary TB to evaluate the impact of adjunctive immune
132 n the highly susceptible guinea pig model of pulmonary TB, a model noteworthy for its close resemblan
133 otype of MCs was studied in 11 necropsies of pulmonary TB and 3 necropsies of non-TB infected lungs t
134 of follow-up, there were 55 observations of pulmonary TB in 52 persons, 26 observations of extrapulm
135 of age and BMI identified five phenotypes of pulmonary TB with significant differences at initial cli
136 populations (HIV/AIDS patients, survivors of pulmonary TB, cancer, chronic obstructive pulmonary dise
140 mmune modulation to improve the treatment of pulmonary TB and reduce the risk of chronic respiratory
141 thesized that aerosol IFN-gamma treatment of pulmonary TB would increase expression of genes importan
143 ve pulmonary TB (on treatment for 1-4 mo) or pulmonary TB treated at least 12 months before study ent
144 deep learning framework to detect pediatric pulmonary TB by identifying TB-compatible CXRs with cons
146 were obtained for cases of culture-positive pulmonary TB (PTB; 91.3%) and extrapulmonary TB (EPTB; 9
147 pproximately 54 (74%) of 72 culture-positive pulmonary TB cases over a 1-year period while requiring
148 lates from patients who had culture-positive pulmonary TB in Iqaluit, Nunavut, between 2009 and 2015
149 Comparison of serum from culture-positive pulmonary TB patients and TB suspects systematically rul
152 um samples from patients with smear-positive pulmonary TB who were consecutively enrolled at 10 inter
153 ial in which individuals with smear-positive pulmonary TB with isoniazid resistance mediated by an in
156 was conducted using sputa from 426 possible pulmonary TB subjects from two small Mexican cities bord
158 Hospital, Thailand, 204 adults with presumed pulmonary TB and negative Xpert MTB/RIF Ultra results or
159 NMR (bNMR) in Nigerian adults with presumed pulmonary TB, including individuals with and without HIV
160 rts, restricted to children with presumptive pulmonary TB < 10 years, and including children in high-
162 re effective vaccination strategy to prevent pulmonary TB, the most common and contagious form of the
163 ine to participants with current or previous pulmonary TB induced a robust immune response and is not
165 the overwhelming majority of culture-proven pulmonary TB cases are diagnosed from the first or secon
166 monary TB compared with patients with purely pulmonary TB (p = 0.01) and was amplified 2.6-fold at di
171 lder, had been diagnosed with drug-sensitive pulmonary TB in the past 4 weeks, smoked daily, were wil
172 bacteriologically confirmed, drug-sensitive pulmonary TB who were eligible to start first-line anti-
174 s safe for the treatment of drug-susceptible pulmonary TB (DS-PTB) compared with the standard 6-month
175 ding all adults treated for drug-susceptible pulmonary TB at 18 health facilities across Uganda over
176 ngitudinal cohort study, 40 drug-susceptible pulmonary TB patients (aged 18-69 years; 60% male) were
178 nts with culture-confirmed, drug-susceptible pulmonary TB who started first-line anti-TB therapy and
180 dentified patients with rifampin-susceptible pulmonary TB were enrolled in a first-in-human study(4)
181 ncluded culture-confirmed, drug-susceptible, pulmonary TB participants receiving standard treatment i
182 c sputum evaluation with Xpert for suspected pulmonary TB, in each of 3 emblematic settings: an HIV c
186 conditional logistic regression models, the pulmonary TB odds ratios (95% confidence intervals) for
192 nal study that recruited 50 adolescents with pulmonary TB and 50 controls exposed to TB in Cape Town,
194 V)-infected and 416 HIV-negative adults with pulmonary TB at the time of initiating chemotherapy and
195 rculosis Severity study compared adults with pulmonary TB in Chennai, India, who were classified as h
197 A, in adults who have had close contact with pulmonary TB patients living in TB-endemic areas, is a s
198 hese individuals to residents diagnosed with pulmonary TB at local health facilities and a representa
199 uated adult patients who were diagnosed with pulmonary TB from 2009 to 2014 in King County, Washingto
205 by monocytes, compared with individuals with pulmonary TB, despite having lower IgG titres and Fcgamm
207 -CCP and anti-CAP in sera from patients with pulmonary TB (n = 49), RA patients (n = 36), and control
208 ccal swabs were collected from patients with pulmonary TB (n = 7), TB-exposed persons (n = 7), and co
209 ere evaluated in 358 Cambodian patients with pulmonary TB and 106 tuberculin-positive control subject
212 weeks of TB treatment from 39 patients with pulmonary TB from Kampala, Uganda enrolled in the Center
213 ith pulmonary TB.METHODSThirty patients with pulmonary TB were enrolled within 7 days of initiating a
214 veolar lavage (BAL) cells from patients with pulmonary TB would have increased spontaneous release of
216 oad-spectrum MMP inhibitor, in patients with pulmonary TB.METHODSThirty patients with pulmonary TB we
217 up 1), 200 household contacts of people with pulmonary TB (Group 2), and 50 with a recent history of
218 e of a novel 4-month regimen for people with pulmonary TB and a shortened 4-month regimen for childre
221 agnostic features, we enrolled subjects with pulmonary TB (N = 149) and controls with other respirato