# The effect of amphetamine-type stimulants on immune response in HIV-infected individuals: a retrospective cohort study

**Authors:** Tao Li, Zuoliang Li, Hai Liu, Jinsi Chen, Yanwei Li, Xin Zhou, Su Zhang, Bei Li, Yulan Ren

PMC · DOI: 10.3389/fimmu.2026.1775159 · Frontiers in Immunology · 2026-02-09

## TL;DR

Amphetamine abuse worsens immune recovery in HIV patients, even with good treatment adherence, suggesting a need for targeted care.

## Contribution

First study to show ATS abuse delays immune recovery in HIV patients on ART, using large-scale real-world data.

## Key findings

- ATS users had lower immune response rates and slower CD4+ T-cell recovery after ART initiation.
- ATS exposure was an independent risk factor for poor immune response (HR: 0.558, P<0.001).
- Longer ATS exposure correlated with reduced immune response rates in HIV patients.

## Abstract

The co-occurrence of amphetamine-type stimulant (ATS) abuse and HIV infection is prevalent, yet the impact of ATS abuse history on immune reconstitution in people living with HIV (PLWH) remains uncertain. We aim to assess the impact of ATS abuse history on immune reconstitution in PLWH with low CD4+ levels and high ART adherence.

Using data from China’s National Free Antiretroviral Treatment Program and Drug Rehabilitation Management Platform data, we identified PLWH who met the inclusion criteria between 2016 and 2022. Propensity score matching paired participants. Primary outcomes focused on immune response after 2 years of ART, and secondary outcomes including CD4+ T-cell count recovery, net increase in CD4+ T-cell count, CD4+ T-cell growth rate, time to immune response, and AIDS-related mortality.

After matching 2,372 PLWH into ATS and non-ATS cohorts, the ATS group exhibited lower immune response rates, delayed responses, smaller increases in CD4+ T-cell counts, and slower initial CD4+ T-cell growth, although growth rates were comparable at later time points. Cox regression analysis identified ATS exposure as an independent risk factor for poorer immune responses 2 years after ART initiation [HR: 0.558 (0.485-0.643), P<0.001]. Kaplan-Meier analysis demonstrated a lower cumulative immune response rate in the ATS group. Longer ATS exposure was associated with reduced immune response rates in PLWH after ART initiation.

A history of ATS abuse hinders HIV immune reconstitution, underscoring the need for tailored services for PLWH with ATS exposure.

## Linked entities

- **Diseases:** AIDS (MONDO:0012268)

## Full-text entities

- **Genes:** 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}
- **Diseases:** HL (MESH:C538324), syphilis (MESH:D013587), Death (MESH:D003643), mitochondrial injury (MESH:D028361), ATS (MESH:D019969), infections (MESH:D007239), drug use (MESH:D019966), immune response failure (MESH:D051437), sexually transmitted infections (MESH:D012749), malignancies (MESH:D009369), opportunistic infection (MESH:D009894), end-stage organ failure (MESH:D007676), immune dysfunction (MESH:D007154), hepatitis C (MESH:D019698), hepatitis B (MESH:D006509), PLWH (MESH:C000719191), /AIDS (MESH:D000163), tuberculosis (MESH:D014376), HIV (MESH:D015658), communicable (MESH:D003141)
- **Chemicals:** ATS (-), methamphetamine (MESH:D008694), amphetamine (MESH:D000661)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606], Human immunodeficiency virus 1 (no rank) [taxon 11676]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12926158/full.md

## References

51 references — full list in the complete paper: https://tomesphere.com/paper/PMC12926158/full.md

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Source: https://tomesphere.com/paper/PMC12926158