Abstract:Purpose of Review
The pulmonary complications of chronic HIV infection have shifted from
infectious complications towards non-infectious pulmonary complications, predominantly chronic obstructive pulmonary disease (COPD). While the best-established COPD risk factor is cigarette smoking, emerging data suggest HIV infection also independently increases COPD risk. The purpose of this article is to review these data and the conflicting data regarding the role of antiretroviral therapy (ART) in modifying COPD risk.… Show more
“…The same authors also reported that higher CD4 counts and undetectable viral loads were protective factors for CAP in the multivariate analysis, as were pneumococcal and influenza vaccinations. Despite effective ART, bacterial CAP is still frequent in HIV-A c c e p t e d M a n u s c r i p t infected patients (17,18), and mortality rates may be rising due to the prevalence of comorbidities in CAP patients (19). A prospective study(7) analyzing more than 18,000 patients in 34 countries over the period 2006 to 2011 reported a pneumonia incidence of 0.53 cases/100 person-years.…”
Section: Epidemiologymentioning
confidence: 99%
“…We recommend that such patients do not need treatment, admission, or care sites that differs from that of the general population. 13,14,15,17,18,19,20,22,23,24,25,27,28,29,30,62,63,66,67,68,70,71 A c c e p t e d M a n u s c r i p t…”
Despite active antiretroviral therapy (ART), community-acquired pneumonia (CAP) remains a major cause of morbidity and mortality among human immunodeficiency virus (HIV)-infected patients and incurs high health costs. Areas covered: This article reviews the most recent publications on bacterial CAP in the HIV-infected population, focusing on epidemiology, prognostic factors, microbial etiology, therapy, and prevention. The data discussed here were mainly obtained from a non-systematic review using Medline, and references from relevant articles. Expert commentary: HIV-infected patients are more susceptible to bacterial CAP. Although ART improves their immune response and has reduced CAP incidence, these patients continue to present increased risk of pneumonia in part because they show altered immunity and because immune activation persists. The risk of CAP in HIV-infected patients and the probability of polymicrobial or atypical infections are inversely associated with the CD4 cell count. Mortality in HIV-infected patients with CAP ranges from 6% to 15% but in well-controlled HIV-infected patients on ART the mortality is low and similar to that seen in HIV-negative individuals. Vaccination and smoking cessation are the two most important preventive strategies for bacterial CAP in well-controlled HIV-infected patients on ART.
“…The same authors also reported that higher CD4 counts and undetectable viral loads were protective factors for CAP in the multivariate analysis, as were pneumococcal and influenza vaccinations. Despite effective ART, bacterial CAP is still frequent in HIV-A c c e p t e d M a n u s c r i p t infected patients (17,18), and mortality rates may be rising due to the prevalence of comorbidities in CAP patients (19). A prospective study(7) analyzing more than 18,000 patients in 34 countries over the period 2006 to 2011 reported a pneumonia incidence of 0.53 cases/100 person-years.…”
Section: Epidemiologymentioning
confidence: 99%
“…We recommend that such patients do not need treatment, admission, or care sites that differs from that of the general population. 13,14,15,17,18,19,20,22,23,24,25,27,28,29,30,62,63,66,67,68,70,71 A c c e p t e d M a n u s c r i p t…”
Despite active antiretroviral therapy (ART), community-acquired pneumonia (CAP) remains a major cause of morbidity and mortality among human immunodeficiency virus (HIV)-infected patients and incurs high health costs. Areas covered: This article reviews the most recent publications on bacterial CAP in the HIV-infected population, focusing on epidemiology, prognostic factors, microbial etiology, therapy, and prevention. The data discussed here were mainly obtained from a non-systematic review using Medline, and references from relevant articles. Expert commentary: HIV-infected patients are more susceptible to bacterial CAP. Although ART improves their immune response and has reduced CAP incidence, these patients continue to present increased risk of pneumonia in part because they show altered immunity and because immune activation persists. The risk of CAP in HIV-infected patients and the probability of polymicrobial or atypical infections are inversely associated with the CD4 cell count. Mortality in HIV-infected patients with CAP ranges from 6% to 15% but in well-controlled HIV-infected patients on ART the mortality is low and similar to that seen in HIV-negative individuals. Vaccination and smoking cessation are the two most important preventive strategies for bacterial CAP in well-controlled HIV-infected patients on ART.
“…With the advent of ART and the improvement of the immune status in patients receiving ART, infectious complications of AIDS are now better controlled. Currently, noninfectious lung diseases, like chronic obstructive pulmonary disease (COPD), are emerging as key clinical conditions [ 85 ].…”
Section: Use Of Nhps To Model Respiratory Comorbiditiesmentioning
With the advent of antiretroviral therapy that can control virus replication below the detection levels of conventional assays, a new clinical landscape of AIDS emerged, in which non-AIDS complications prevail over AIDS-defining conditions. These comorbidities are diverse and affect multiple organs, thus resulting in cardiovascular, kidney, neurocognitive and liver disease, osteopenia/osteoporosis, and cancers. A common feature of these conditions is that they are generally associated with accelerated aging. The mechanism behind these comorbidities is chronic excessive inflammation induced by HIV infection, which persists under antiretroviral therapy. Progressive simian immunodeficiency virus (SIV) infection of nonhuman primates (NHPs) closely reproduces these comorbidities and offers a simplified system in which most of the traditional human risk factors for comorbidities (i.e., smoking, hyperlipidemia) are absent. Additionally, experimental conditions can be properly controlled during a shorter course of disease for SIV infection. As such, NHPs can be employed to characterize new paradigms of AIDS pathogenesis and to test the efficacy of interventions aimed at alleviating non-AIDS-related comorbidities.
“…Even in the modern ART era, persons with HIV are at a greater risk of developing both infectious and noninfectious pulmonary diseases than persons without HIV. For example, persons with HIV infection are at elevated risk for invasive Streptococcal pneumoniae infection, as well as chronic obstructive pulmonary disease (COPD) 5,6 . Furthermore, coinfection of tuberculosis (TB) and HIV is a significant public health challenge in certain regions of the world, notably, sub-Saharan Africa, as HIV-infected individuals are 16 to 27 times more likely to have TB than persons without HIV 7 .…”
Section: Introductionmentioning
confidence: 99%
“…Although some explanations for this susceptibility to pulmonary infection and chronic disease have been proposed 8,9,10 , the precise cellular mechanisms by which individuals with suppressed HIV plasma viral load remain at higher risk for pulmonary complications have not been fully elucidated. Importantly, HIV is a very strong risk factor for pulmonary infection and chronic disease, independent of smoking status 6 .…”
Bronchoscopy is a medical procedure whereby normal saline is injected into the lungs via a bronchoscope and then suction is applied, removing bronchoalveolar lavage (BAL) fluid. The BAL fluid is rich in cells and can thus provide a 'snapshot' of the pulmonary immune milieu. CD4 T cells are the best characterized HIV reservoirs, while there is strong evidence to suggest that tissue macrophages, including alveolar macrophages (AMs), also serve as viral reservoirs. However, much is still unknown about the role of AMs in the context of HIV reservoir establishment and maintenance. Therefore, developing a protocol for processing BAL fluid to obtain cells that may be used in virological and immunological assays to characterize and evaluate the cell populations and subsets within the lung is relevant for understanding the role of the lungs as HIV reservoirs. Herein, we describe such a protocol, employing standard techniques such as simple centrifugation and flow cytometry. The CD4 T cells and AMs may then be used for subsequent applications, including immunophenotyping and HIV DNA and RNA quantification.
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