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Camilla Tincati

Researcher at University of Milan

Publications -  81
Citations -  2512

Camilla Tincati is an academic researcher from University of Milan. The author has contributed to research in topics: Medicine & Immune system. The author has an hindex of 19, co-authored 66 publications receiving 2062 citations. Previous affiliations of Camilla Tincati include University of California, San Francisco & Université de Montréal.

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Microbial Translocation in the Pathogenesis of HIV Infection and AIDS

TL;DR: In vivo studies demonstrated that HIV/SIV-associated microbial translocation results from a series of immunopathological events occurring at the GI mucosa, and a key pathogenic event appears to be innate immunity activation via Toll-like receptors and other pathogen recognition receptors.
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Microbial translocation is associated with sustained failure in CD4+ T-cell reconstitution in HIV-infected patients on long-term highly active antiretroviral therapy.

TL;DR: Higher circulating lipopolysaccharide associated with plasma enterobacterial DNA and highly activated Ki67+CD4+CD8+ in 24 immunologic-nonresponders compared with 11 full responders provides novel insight into INRs pathogenesis, since they correlate augmented systemic translocation of microbial bioproducts with T-cell hyperactivation.
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Early Impairment of Gut Function and Gut Flora Supporting a Role for Alteration of Gastrointestinal Mucosa in Human Immunodeficiency Virus Pathogenesis

TL;DR: Results show that impairment of the gastrointestinal tracts in human immunodeficiency virus (HIV)-positive patients is present in the early phases of HIV disease, and this impairment is associated with alterations in gut microbiota and intestinal inflammatory parameters.
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The Absence of CD4+ T Cell Count Recovery Despite Receipt of Virologically Suppressive Highly Active Antiretroviral Therapy: Clinical Risk, Immunological Gaps, and Therapeutic Options

TL;DR: A thorough assessment of the clinical implications of a lack of increase in the CD4(+) T cell count in immunological nonresponders is provided, to examine the immunological gaps limiting recovery of the CD 4(+)T cell count, and to note possible therapeutic avenues, which may offer clinicians guidance regarding how to most efficaciously treat these critical patients.