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High prevalence of gastrointestinal manifestations among Cytomegalovirus end-organ disease in the combination antiretroviral era

  1. Author:
    Caplan, Margaret R.
    Wilson, Eleanor M. P.
    Schechter, Melissa
    Cai, Catherine W.
    Venner, Allison
    Bishop, Rachel
    Adelsberger, Joseph
    Higgins, Jeanette
    Roby, Gregg
    Wang, Jing
    Sheikh, Virginia
    Sereti, Irini
  2. Author Address

    Clin Res Directorate, Frederick Natl Lab Canc Res, Bethesda, MD 20817 USA.Natl Inst Hlth, Natl Inst Allergy & Infect Dis, Immunoregulat Lab, 10 Ctr Dr,CRC,Rm 11-B15, Bethesda, MD 20892 USA.Natl Inst Hlth, Natl Eye Inst, Bethesda, MD 20892 USA.Leidos Biomed Res Inc, Frederick Natl Lab Canc Res, Frederick, MD 21701 USA.Frederick Natl Lab Canc Res, Clin Monitoring Res Program Directorate, Frederick, MD 21701 USA.Cty Angeles, Dept Publ Hlth, Los Angeles, CA 90012 USA.Univ Maryland, Dept Med, Sch Med, Baltimore, MD 21201 USA.GI Consultants, Carson City, NV 89703 USA.
    1. Year: 2021
    2. Date: Sep 9
    3. Epub Date: 2021 Sep
  1. Journal: Journal of Virus Eradication
  2. Mediscript Ltd
    1. 7
    2. 3
  3. Type of Article: Article
  4. Article Number: ARTN 100052
  5. ISSN: 2055-6640
  1. Abstract:

    Background: Cytomegalovirus (CMV) end-organ disease (EOD) continues to pose a significant risk to patients with advanced HIV disease despite decreased incidence with combination anti-retroviral therapy (ART) and lower mortality with effective anti-CMV therapy. Subclinical CMV shedding may also contribute to ongoing inflam-mation and non-infectious comorbidities. Methods: We examined the occurrence of CMV EOD and CMV shedding in a cohort of patients participating in a prospective observational study of severely immunosuppressed (CD4 <= 100 cells/mu l), ART-naive, HIV-1 infected adult participants. Results: We studied 206 participants, of whom 193 (93.7%) were CMV IgG positive. Twenty-five participants (12.1%) developed confirmed CMV EOD. At baseline, 47 (22.8%) had CMV viremia detectable by PCR in the absence of clinical disease (CMV viremia). The remaining 134 (65%) had neither CMV EOD nor CMV viremia detected at baseline. Five participants with CMV EOD (2.4% of total cohort, 20% of CMV EOD) met AIDS Clinical Trials Group criteria for CMV immune reconstitution inflammatory syndrome (IRIS). Only one-third of CMV EOD patients had retinitis, while two-thirds presented with histologically confirmed gastrointestinal illness. CMV viremia was associated with higher percentages of activated CD8(+) T cells even after HIV suppression. Conclusion: The manifestations of CMV EOD in advanced HIV disease before and after initiation of ART may be more diverse than previously described, with high incidence of gastrointestinal illness. Recognition and treat-ment of unusual clinical presentations of CMV infection remains important in reducing morbidity and mortality from HIV co-infections.

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External Sources

  1. DOI: 10.1016/j.jve.2021.100052
  2. PMID: 34557308
  3. PMCID: PMC8446803
  4. WOS: 000704578700002

Library Notes

  1. Fiscal Year: FY2020-2021
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