# The impact of human immunodeficiency virus coinfection on mpox patients during the 2022 global outbreak: a systematic review and meta-analysis based on comparative observational studies

**Authors:** Yingying Han, Xingzhao Li, Xin Wang, Zhuan Zhong

PMC · DOI: 10.3389/fmicb.2026.1751445 · 2026-02-09

## TL;DR

This study found that people with HIV who contracted mpox in 2022 had more severe symptoms, worse outcomes, and higher mortality compared to those without HIV.

## Contribution

The study is the first systematic review and meta-analysis to quantify how HIV coinfection affects mpox disease severity and clinical outcomes.

## Key findings

- HIV-positive mpox patients were older and more likely to be men who have sex with men.
- HIV coinfection was linked to more severe mpox, higher hospitalization rates, and increased mortality.
- HIV-positive patients had lower CD4+ T-cell counts and hemoglobin levels compared to HIV-negative patients.

## Abstract

The mpox outbreak in 2022 posed a new challenge to the medical system. We aimed to study the impact of human immunodeficiency virus (HIV) coinfection on mpox patients.

This study was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines.

Our study included 27 articles for meta-analysis and divided mpox patients into two groups: one group was HIV-positive, and the other group was HIV-negative. We found that the age of HIV-positive patients was significantly greater than that of HIV-negative patients (SMD = 0.35, 95% CI: 0.29–0.41) and that there were more men who had sex with men in the HIV-positive group (OR = 3.98, 95% CI: 3.04–5.21). Syphilis (OR = 2.66, 95% CI: 2.13–3.33), hepatitis B (OR = 3.94, 95% CI: 2.93–5.30), hepatitis C (OR = 5.71, 95% CI: 3.06–10.64), proctitis (OR = 1.52, 95% CI: 1.17–1.98), fever (OR = 1.15, 95% CI: 1.01–1.30), diarrhea (OR = 1.69, 95% CI: 1.03–2.77) and pustules (OR = 1.33, 95% CI: 1.08–1.62) were more common among HIV-positive patients. HIV coinfection seemed to be associated with a decrease in the CD4+ T-cell count (SMD = −0.78, 95% CI: −1.34 to −0.23) and hemoglobin (SMD = −0.43, 95% CI: −0.64 to −0.22) and albumin (SMD = −0.35, 95% CI: −0.55 to −0.15) levels, whereas the CD8+ T-cell count yielded the opposite statistical conclusion (SMD = 0.35, 95% CI: 0.03–0.67). We also found that HIV-positive patients had more hospitalizations (OR = 1.63, 95% CI: 1.22–2.19), more severe mpox (OR = 1.82, 95% CI: 1.28–2.58), more need for tecovirimat treatment (OR = 4.25, 95% CI: 1.59–11.4), and higher mortality (OR = 3.36, 95% CI: 1.15–9.83).

Overall, HIV coinfection may influence the disease process and clinical indicators of mpox patients and is associated with more severe clinical outcomes.

https://www.crd.york.ac.uk/PROSPERO/view/CRD420251056729, PROSPERO registration number: CRD420251056729.

## Linked entities

- **Diseases:** syphilis (MONDO:0005976), hepatitis B (MONDO:0005344)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, CCL4 (C-C motif chemokine ligand 4) [NCBI Gene 6351] {aka ACT2, AT744.1, G-26, HC21, LAG-1, LAG1}, CSF3 (colony stimulating factor 3) [NCBI Gene 1440] {aka C17orf33, CSF3OS, GCSF}, CCL3 (C-C motif chemokine ligand 3) [NCBI Gene 6348] {aka G0S19-1, LD78, LD78ALPHA, MIP-1-alpha, MIP1A, SCI}
- **Diseases:** sore throat (MESH:D010612), immunodeficiency (MESH:D007153), deaths (MESH:D003643), viral diseases (MESH:D014777), HIV coinfection (MESH:D060085), gonorrhea (MESH:D006069), arthralgia (MESH:D018771), infected (MESH:D007239), rectal pain (MESH:C563475), myalgia (MESH:D063806), bacterial infection (MESH:D001424), herpes (MESH:C536395), chlamydia (MESH:D002690), HIV (MESH:D015658), asthenia (MESH:D001247), tonsillitis (MESH:D014069), rectal inflammation (MESH:D007249), headache (MESH:D006261), Syphilis (MESH:D013587), hepatitis B (MESH:D006509), hepatitis C (MESH:D019698), sexually transmitted diseases (MESH:D012749), urethritis (MESH:D014526), opportunistic infections (MESH:D009894), HIV viremia (MESH:D014766), diarrhea (MESH:D003967), pneumonia (MESH:D011014), lymphadenopathy (MESH:D008206), febrile rash (MESH:D005076), AIDS[Title (MESH:D000163), nausea (MESH:D009325), proctitis (MESH:D011349), vomiting (MESH:D014839), Fever (MESH:D005334)
- **Chemicals:** mpox (MESH:C051836), acyl hydrazide (-), creatine (MESH:D003401), creatinine (MESH:D003404), bilirubin (MESH:D001663), Tecovirimat (MESH:C505045)
- **Species:** Human immunodeficiency virus (species) [taxon 12721], Homo sapiens (human, species) [taxon 9606], Variola (genus) [taxon 300414], Human immunodeficiency virus 1 (no rank) [taxon 11676]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12964369/full.md

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Source: https://tomesphere.com/paper/PMC12964369