# Transcriptional signature of induced neurons differentiates virologically suppressed people with HIV from people without HIV

**Authors:** Philipp N. Ostermann, Youjun Wu, Scott A. Bowler, Samuel Martínez-Meza, Mohammad Adnan Siddiqui, David H. Meyer, Alberto Herrera, Brandon A. Sealy, Mega Sidharta, Kiran Ramnarine, Leslie Ann St. Bernard, Desiree Byrd, R. Brad Jones, Masahiro Yamashita, Douglas F. Nixon, Lishomwa C. Ndhlovu, Ting Zhou, Teresa H. Evering

PMC · DOI: 10.1172/jci.insight.190445 · 2025-11-25

## TL;DR

Scientists found a unique gene pattern in brain-like cells from HIV patients that could explain why some people with HIV still face brain issues even when the virus is controlled.

## Contribution

The study identifies a novel transcriptional signature in induced neurons that differentiates HIV-positive individuals from HIV-negative individuals despite viral suppression.

## Key findings

- 29 genes were found to be significantly differentially expressed between HIV-positive and HIV-negative induced neurons.
- PLWH iNs showed altered extracellular matrix organization and synaptic transmission pathways.
- Reduced FOXL2NB-FOXL2-LINC01391 expression correlated with neurocognitive impairment in HIV-positive individuals.

## Abstract

Neurocognitive impairment is a prevalent comorbidity in virologically suppressed people living with HIV (PLWH), yet the underlying mechanisms remain elusive and treatments lacking. We explored use of participant-derived directly induced neurons (iNs) to model neuronal biology and injury in PLWH. iNs retain age- and disease-related donor features, providing unique opportunities to reveal important aspects of neurological disorders. We obtained primary dermal fibroblasts from 6 virologically suppressed PLWH and 7 matched people without HIV (PWOH). iNs were generated using transcription factors NGN2 and ASCL1 and validated by immunocytochemistry, single-cell RNA-Seq, and electrophysiological recordings. Transcriptomic aging analyses confirmed retention of donor age-related signatures. Bulk RNA-Seq identified 29 significantly differentially expressed genes between PLWH and PWOH iNs. Of these, 16 were downregulated and 13 upregulated in PLWH iNs. Protein-protein interaction network mapping indicated iNs from PLWH exhibited differences in extracellular matrix organization and synaptic transmission. IFI27 was upregulated in PLWH iNs, complementing independent postmortem studies demonstrating elevated IFI27 expression in PLWH-derived brain tissue. FOXL2NB-FOXL2-LINC01391 expression was reduced in PLWH iNs and negatively correlated with neurocognitive impairment. Thus, we identified an iN gene signature of HIV revealing mechanisms of neurocognitive impairment in PLWH.

Direct reprogramming of skin fibroblasts into neurons reveals unique gene signatures indicative of HIV infection in the context of viral suppression.

## Linked entities

- **Genes:** NEUROG2 (neurogenin 2) [NCBI Gene 63973], ASCL1 (achaete-scute family bHLH transcription factor 1) [NCBI Gene 429], IFI27 (interferon alpha inducible protein 27) [NCBI Gene 3429], FOXL2NB (FOXL2 neighbor) [NCBI Gene 401089], FOXL2 (forkhead box L2) [NCBI Gene 668], LINC01391 (long intergenic non-protein coding RNA 1391) [NCBI Gene 103344930]

## Full-text entities

- **Genes:** FOXL2NB (FOXL2 neighbor) [NCBI Gene 401089] {aka C3orf72}, FOXL2 (forkhead box L2) [NCBI Gene 668] {aka BPES, BPES1, PFRK, PINTO, POF3}, LINC01391 (long intergenic non-protein coding RNA 1391) [NCBI Gene 103344930], IFI27 (interferon alpha inducible protein 27) [NCBI Gene 3429] {aka FAM14D, ISG12, ISG12A, P27}, ASCL1 (achaete-scute family bHLH transcription factor 1) [NCBI Gene 429] {aka ASH1, HASH1, MASH1, bHLHa46}, NEUROG2 (neurogenin 2) [NCBI Gene 63973] {aka Atoh4, Math4A, NGN2, bHLHa8, ngn-2}
- **Diseases:** neurological disorders (MESH:D009461), Neurocognitive impairment (MESH:D019965)
- **Species:** Human immunodeficiency virus 1 (no rank) [taxon 11676], Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12892921/full.md

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Source: https://tomesphere.com/paper/PMC12892921