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T-cell immunity against cytomegalovirus in HIV infection and aging: relationships with inflammation, immune activation, and frailty

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  1. Bacterial aggregate size determines phagocytosis efficiency of polymorphonuclear leukocytes

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  2. Defective interferon priming and impaired antiviral responses in a patient with an IRF7 variant and severe influenza

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  3. P. aeruginosa flow-cell biofilms are enhanced by repeated phage treatments but can be eradicated by phage-ciprofloxacin combination

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Both aging and treated human immunodeficiency virus (HIV) infection are characterized by low-level chronic inflammation and immune activation which contribute to the development of age-related diseases, frailty, and early mortality. Chronic cytomegalovirus (CMV) infection is highly prevalent in older adults and HIV-infected populations. A number of studies have shown that CMV induces broad and strong T-cell responses in CMV-seropositive older adults and HIV-infected individuals. CMV infection rarely develops into clinical disease in immunocompetent individuals. However, a large body of literature has shown adverse effects of chronic CMV infection on the health and longevity of these populations. It has been hypothesized that chronic CMV infection may be a driver of chronic inflammation and immune activation, and may further contribute to the development of frailty. Thus, there is a need to better understand the extent of the impact of chronic CMV infection on T-cell immunity and health in aging and HIV infection. In this review, we will address important considerations and challenges in the assessment of chronic CMV infection and CMV-specific T-cell responses. We will then review recent data on relationships between T-cell responses to CMV and levels of inflammatory markers and immune activation, as well as the onset of frailty.

Original languageEnglish
JournalMedical Microbiology and Immunology
Volume208
Issue number3-4
Pages (from-to)289-294
Number of pages6
ISSN0300-8584
DOIs
Publication statusPublished - Aug 2019

    Research areas

  • Aging, CLIP, Cytomegalovirus, Frailty, HIV infection, Immune activation

ID: 56892117