# The Long Shadow of Early HCMV–HIV Coinfection: Epidemiology, Pathogenesis, and Immune Consequences

**Authors:** Camilla Albano, Francesca Gugliesi, Greta Bajetto, Beatrice Braga, Valentina Dell’Oste, Gloria Griffante, Selina Pasquero

PMC · DOI: 10.3390/children13020236 · 2026-02-07

## TL;DR

This paper reviews how early co-infection with HCMV and HIV affects children's health, including immune consequences and long-term risks.

## Contribution

The paper integrates recent findings with historical data to highlight gaps in understanding HCMV–HIV coinfection in pediatric populations.

## Key findings

- HCMV coinfection in HIV-positive children is linked to severe disease and high mortality.
- HCMV may accelerate HIV progression and immune dysregulation through synergistic mechanisms.
- HEU newborns have higher HCMV infection rates and worse outcomes compared to HIV-unexposed children.

## 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.

## Linked entities

- **Diseases:** AIDS (MONDO:0012268), immunodeficiency (MONDO:0021094)

## Full-text entities

- **Genes:** KLRC2 (killer cell lectin like receptor C2) [NCBI Gene 3822] {aka CD159c, NKG2-C, NKG2C}, PTPRC (protein tyrosine phosphatase receptor type C) [NCBI Gene 5788] {aka B220, CD45, CD45R, GP180, IMD105, L-CA}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, CCR7 (C-C motif chemokine receptor 7) [NCBI Gene 1236] {aka BLR2, CC-CKR-7, CCR-7, CD197, CDw197, CMKBR7}, B3GAT1 (beta-1,3-glucuronyltransferase 1) [NCBI Gene 27087] {aka CD57, GLCATP, GLCUATP, HNK1, LEU7, NK-1}, IL2RB (interleukin 2 receptor subunit beta) [NCBI Gene 3560] {aka CD122, IL15RB, IMD63, P70-75}, NCAM1 (neural cell adhesion molecule 1) [NCBI Gene 4684] {aka CD56, MSK39, NCAM}, CR2 (complement C3d receptor 2) [NCBI Gene 1380] {aka C3DR, CD21, CR, CVID7, SLEB9}, IL2RA (interleukin 2 receptor subunit alpha) [NCBI Gene 3559] {aka CD25, IDDM10, IL2R, IMD41, TCGFR, p55}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, CDKN2A (cyclin dependent kinase inhibitor 2A) [NCBI Gene 1029] {aka ARF, CAI2, CDK4I, CDKN2, CMM2, INK4}, TAT (tyrosine aminotransferase) [NCBI Gene 6898], IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CCR5 (C-C motif chemokine receptor 5) [NCBI Gene 1234] {aka CC-CKR-5, CCCKR5, CCR-5, CD195, CKR-5, CKR5}, MME (membrane metalloendopeptidase) [NCBI Gene 4311] {aka CALLA, CD10, CMT2T, NEP, SCA43, SFE}, CXCL10 (C-X-C motif chemokine ligand 10) [NCBI Gene 3627] {aka C7, IFI10, INP10, IP-10, SCYB10, crg-2}, KLRD1 (killer cell lectin like receptor D1) [NCBI Gene 3824] {aka CD94}, CD28 (CD28 molecule) [NCBI Gene 940] {aka IMD123, Tp44}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, ITIH4 (inter-alpha-trypsin inhibitor heavy chain 4) [NCBI Gene 3700] {aka GP120, H4P, IHRP, ITI-HC4, ITIHL1, PK-120}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, KLRG1 (killer cell lectin like receptor G1) [NCBI Gene 10219] {aka 2F1, CLEC15A, MAFA, MAFA-2F1, MAFA-L, MAFA-LIKE}, IL7 (interleukin 7) [NCBI Gene 3574] {aka IL-7, IMD130}, CD27 (CD27 molecule) [NCBI Gene 939] {aka S152, S152. LPFS2, T14, TNFRSF7, Tp55}, H3P16 (H3 histone pseudogene 16) [NCBI Gene 644914] {aka H3.6, H3F3AP6, p21}, CX3CR1 (C-X3-C motif chemokine receptor 1) [NCBI Gene 1524] {aka CCRL1, CMKBRL1, CMKDR1, GPR13, GPRV28, V28}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, IL7R (interleukin 7 receptor) [NCBI Gene 3575] {aka CD127, CDW127, IL-7R-alpha, IL-7Ralpha, IL7RA, IL7Ralpha}
- **Diseases:** impaired growth and neurodevelopment (MESH:D006130), inflammation (MESH:D007249), injury to (MESH:D014947), intrauterine growth restriction (MESH:D005317), cardiometabolic alterations (MESH:D024821), hepatosplenomegaly (MESH:C535727), permanent disability (MESH:D003638), malignancy (MESH:D009369), opportunistic infections (MESH:D009894), Morbidity (OMIM:614963), HCMV viremia (MESH:D014766), jaundice (MESH:D007565), microcephaly (MESH:D008831), pneumonia (MESH:D011014), stroke (MESH:D020521), AIDS (MESH:D000163), rash (MESH:D005076), Congenital HCMV (cCMV) infection (MESH:D003586), arteriopathy (MESH:D020212), HIV-associated vasculopathy (MESH:D016263), esophagitis (MESH:D004941), SNHL (MESH:D006319), seizures (MESH:D012640), hearing impairment (MESH:D034381), neurological abnormalities (MESH:D009461), death (MESH:D003643), immunodeficiency (MESH:D007153), encephalopathy (MESH:D001927), congenital viral infection (MESH:D014777), HCMV Coinfection (MESH:D060085), Cerebrovascular abnormalities (MESH:D002561), MTCT (MESH:C562515), congenital infection (MESH:D007239), cardiovascular disease (MESH:D002318), end-organ damage (MESH:C564816), retinitis (MESH:D012173), immune dysfunction (MESH:D007154), hepatitis (MESH:D056486), HIV infection or infant death (MESH:D066088), enteritis (MESH:D004751), type 2 diabetes (MESH:D003924), tissue damage (MESH:D017695), auditory and neurological sequelae (MESH:D009422), chronic (MESH:D002908), immune dysregulation (OMIM:614878), HEU (MESH:D015658)
- **Species:** Cowpea chlorotic mottle virus (no rank) [taxon 12303], Human immunodeficiency virus 1 (no rank) [taxon 11676], Human immunodeficiency virus (species) [taxon 12721], Homo sapiens (human, species) [taxon 9606], Human betaherpesvirus 5 (no rank) [taxon 10359]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12940063/full.md

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Source: https://tomesphere.com/paper/PMC12940063