# Antiretroviral treatment does not prevent extrapulmonary tuberculosis during SIV/Mtb coinfection in macaques

**Authors:** Collin R. Diedrich, Tara Rutledge, Janelle L. Gleim, Christopher Kline, Pauline Maiello, Jessica M. Medrano, H. Jacob Borish, Harris B. Chishti, Justin L. Gaines, Edwin Klein, Forrest Hopkins, Jacob E. Klein, Daniel Fillmore, Kara Kracinovsky, Jaime Tomko, Jennifer Schober, Sarah M. Fortune, Michael C. Chao, JoAnne L. Flynn, Zandrea Ambrose, Philana Ling Lin

PMC · DOI: 10.1172/jci.insight.199314 · JCI Insight · 2026-02-23

## TL;DR

Antiretroviral treatment does not prevent severe tuberculosis in monkeys coinfected with SIV and Mtb.

## Contribution

This study shows that ART does not prevent extrapulmonary TB in SIV/Mtb coinfected macaques despite suppressing SIV.

## Key findings

- SIV-TB animals had greater gross pathology and bacterial burden than TB-only and SIV/ART/TB groups.
- ART-treated SIV/TB macaques showed similar extrapulmonary TB as untreated SIV/TB animals.
- ART did not prevent Mtb extrapulmonary dissemination despite normal CD4 counts and undetectable SIV RNA.

## Abstract

Coinfection with both HIV and M. tuberculosis (Mtb) results in disseminated tuberculosis (TB) and accelerated HIV progression. Despite greater access to antiretroviral treatment (ART), it remains unclear whether suppression of HIV replication protects against severe Mtb infection. Here, using a macaque model of SIV/Mtb coinfection, we investigated whether treatment of SIV infection with ART influenced control of a subsequent Mtb challenge compared with SIV-infected macaques that were not treated with ART. Macaques were first infected with SIVB670, SIVB670 with ART, or saline followed by a low-dose Mtb inoculation with serial clinical and PET-CT imaging assessments. At necropsy, gross pathology, viremia, bacterial burden, and immunologic parameters were compared. SIV-TB animals had greater gross pathology and total bacterial burden than TB-only and SIV/ART/TB groups. However, despite normal blood CD4 counts and undetectable SIV RNA, SIV/ART/TB macaques showed similar clinical parameters and extrapulmonary involvement as SIV/TB animals. Analysis of barcoded-Mtb suggests that ART control of SIV replication did not prevent Mtb extrapulmonary dissemination. These data indicate that people living with HIV on ART remain at high risk of bacterial dissemination and extrapulmonary TB disease. Understanding the mechanisms of extrapulmonary spread and disease severity during HIV/TB coinfection remains an important issue.

Coinfection with HIV and tuberculosis remains a global health threat that is not prevented by antiretroviral therapy.

## Linked entities

- **Diseases:** tuberculosis (MONDO:0018076)

## Full-text entities

- **Genes:** VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, CCL26 (C-C motif chemokine ligand 26) [NCBI Gene 10344] {aka IMAC, MIP-4a, MIP-4alpha, SCYA26, TSC-1}, IL16 (interleukin 16) [NCBI Gene 3603] {aka LCF, NIL16, PRIL16, prIL-16}, LAMP1 (lysosome associated membrane protein 1) [NCBI Gene 3916] {aka CD107a, LAMPA, LGP120}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, CCL3 (C-C motif chemokine ligand 3) [NCBI Gene 6348] {aka G0S19-1, LD78, LD78ALPHA, MIP-1-alpha, MIP1A, SCI}, NELFCD (negative elongation factor complex member C/D) [NCBI Gene 51497] {aka HSPC130, NELF-C, NELF-D, TH1, TH1L}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, IL15 (interleukin 15) [NCBI Gene 3600] {aka IL-15}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, IL7 (interleukin 7) [NCBI Gene 3574] {aka IL-7, IMD130}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, IL5 (interleukin 5) [NCBI Gene 3567] {aka EDF, IL-5, TRF}, IL12B (interleukin 12B) [NCBI Gene 3593] {aka CLMF, CLMF2, IL-12B, IMD28, IMD29, NKSF}, CD69 (CD69 molecule) [NCBI Gene 969] {aka AIM, BL-AC/P26, CLEC2C, EA1, GP32/28, MLR-3}, CSF2 (colony stimulating factor 2) [NCBI Gene 1437] {aka CSF, GMCSF}, CCL22 (C-C motif chemokine ligand 22) [NCBI Gene 6367] {aka A-152E5.1, ABCD-1, DC/B-CK, MDC, SCYA22, STCP-1}, CD38 (CD38 molecule) [NCBI Gene 952] {aka ADPRC 1, ADPRC1, cADPR1}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, CCL2 (C-C motif chemokine ligand 2) [NCBI Gene 6347] {aka GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1}, ITIH4 (inter-alpha-trypsin inhibitor heavy chain 4) [NCBI Gene 3700] {aka GP120, H4P, IHRP, ITI-HC4, ITIHL1, PK-120}, CD14 (CD14 molecule) [NCBI Gene 929], TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, CCL13 (C-C motif chemokine ligand 13) [NCBI Gene 6357] {aka CKb10, MCP-4, NCC-1, NCC1, SCYA13, SCYL1}, 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}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, CXCL10 (C-X-C motif chemokine ligand 10) [NCBI Gene 3627] {aka C7, IFI10, INP10, IP-10, SCYB10, crg-2}
- **Diseases:** lymphadenitis (MESH:D008199), HIV (MESH:D015658), necrosis (MESH:D009336), Viremia (MESH:D014766), lung granulomas (MESH:D016726), loss of appetite (MESH:D001068), Lung inflammation (MESH:D011014), Granulomas (MESH:D006099), Mtb (MESH:D014376), systemic (MESH:D015619), PLWHIV (MESH:C000719191), AIDS (MESH:D000163), bacterial (MESH:D001424), weight loss (MESH:D015431), macrophage dysfunction (MESH:D055501), immune reconstitution inflammatory syndrome (MESH:D054019), dehydration (MESH:D003681), meningitis (MESH:D008580), extrapulmonary (MESH:D000092225), SIVB670 infection (MESH:D007239), pulmonary TB (MESH:D014397), ART (MESH:D016609), thoracic LN (MESH:D013896), immune dysfunction (MESH:D007154), Lung (MESH:D008171), systemic illness (MESH:D012140), death (MESH:D003643), SIV infection (MESH:D016097), liver lesions (MESH:D008107), Coinfection (MESH:D060085), abscess (MESH:D000038), inflammation (MESH:D007249)
- **Chemicals:** ethanol (MESH:D000431), dithiothreitol (MESH:D004229), HCl (MESH:D006851), Isopropanol (MESH:D019840), glycogen (MESH:D006003), chloroform (MESH:D002725), DTG (MESH:C562325), phenol (MESH:D019800), water (MESH:D014867), 1-bromo-3-chloropropane (MESH:C560814), EDTA (MESH:D004492), tenofovir (MESH:D000068698), ionomycin (MESH:D015759), AI11871 (-), Brefeldin A (MESH:D020126)
- **Species:** Macaca (macaque, genus) [taxon 9539], Human immunodeficiency virus 1 (no rank) [taxon 11676], Homo sapiens (human, species) [taxon 9606], Qubevirus faecium (species) [taxon 39804], Mycobacterium tuberculosis (species) [taxon 1773], Cercopithecidae (monkey, family) [taxon 9527], Macaca fascicularis (crab eating macaque, species) [taxon 9541], Macaca mulatta (rhesus macaque, species) [taxon 9544]
- **Mutations:** K15058D

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12956018/full.md

## References

69 references — full list in the complete paper: https://tomesphere.com/paper/PMC12956018/full.md

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Source: https://tomesphere.com/paper/PMC12956018