Evidence map›Paper›PMID 41749592›Full record

ReviewChildren (Basel, Switzerland)2026

The Long Shadow of Early HCMV-HIV Coinfection: Epidemiology, Pathogenesis, and Immune Consequences.

Camilla Albano, Francesca Gugliesi, Greta Bajetto, Beatrice Braga, Valentina Dell'Oste, Gloria Griffante, Selina Pasquero

Abstract readReview
In one paragraph

Review in Children (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Camilla AlbanoDepartment of Public Health and Pediatric Sciences, Medical School, University of Turin, 10124 Turin, Italy.ORCID 0000-0002-0847-6332
Francesca GugliesiDepartment of Public Health and Pediatric Sciences, Medical School, University of Turin, 10124 Turin, Italy.ORCID 0000-0001-6389-5129
Greta BajettoDepartment of Public Health and Pediatric Sciences, Medical School, University of Turin, 10124 Turin, Italy.ORCID 0000-0002-2339-2479
Beatrice BragaDepartment of Public Health and Pediatric Sciences, Medical School, University of Turin, 10124 Turin, Italy.ORCID 0009-0006-3915-8608
Valentina Dell'OsteDepartment of Public Health and Pediatric Sciences, Medical School, University of Turin, 10124 Turin, Italy.ORCID 0000-0002-9336-7906
Gloria GriffanteDepartment of Public Health and Pediatric Sciences, Medical School, University of Turin, 10124 Turin, Italy.ORCID 0000-0002-2578-9621
Selina PasqueroDepartment of Public Health and Pediatric Sciences, Medical School, University of Turin, 10124 Turin, Italy.ORCID 0000-0002-3815-2494

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human cytomegalovirus (HCMV) and Human Immunodeficiency Virus (HIV) are two pathogens known to have dramatic consequences when contracted early in life. In addition to having a significant impact when acquired individually, these two viruses are known to frequently cause coinfections. Indeed, also in the modern era, HCMV remains one of the most prevalent coinfections in newborns of mothers living with HIV, including both HIV-positive children regardless of their immune status, and those exposed to HIV but uninfected (HEU). In children with HIV infection, HCMV coinfection has historically been associated with AIDS-defining disease, high mortality, and prolonged, elevated HCMV viral load. Although timely administration of antiretroviral therapy prevents immunodeficiency in people living with HIV and thus reduces the incidence of full-blown HCMV disease in cases of coinfection, emerging data suggest that HCMV-induced immune activation and aging persist, potentially contributing to long-term, non-AIDS-related comorbidities. Growing evidence indicates that also HCMV amplifies HIV susceptibility, disease progression, and immune dysregulation through multiple synergistic mechanisms. Moreover, congenital and early postnatal HCMV infections occur at significantly higher rates in HEU newborns than in HIV-unexposed children and are associated with worse clinical outcomes, particularly when HCMV viral loads are high. This review summarizes current knowledge on the epidemiology, clinical impact, and immunopathogenetic interactions of early HCMV-HIV coinfection in pediatric populations. By integrating recent findings with historical evidence, it highlights critical mechanistic and epidemiological gaps that warrant further investigation.

Indexed as

cellular senescencecoinfectioncongenital infectionsHCMVHIVimmunosenescencepremature aging

Identifiers

PMID41749592
PMCPMC12940063

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.