# Comparison of Integrase Strand Transfer Inhibitors (INSTIs) and Protease-Boosted Inhibitors (PIs) on the Reduction in Chronic Immune Activation in a Virally Suppressed, Mainly Male Population Living with HIV (PLWH)

**Authors:** Thomas Nitsotolis, Konstantinos G. Kyriakoulis, Anastasios Kollias, Alexia Papalexandrou, Helen Kalampoka, Elpida Mastrogianni, Dimitrios Basoulis, Mina Psichogiou

PMC · DOI: 10.3390/medicina60020331 · 2024-02-15

## TL;DR

This study compares two HIV treatments, INSTIs and PIs, to see which better reduces chronic immune activation in virally suppressed HIV patients, mainly men.

## Contribution

The study provides new insights into the immunological effects of INSTIs versus PIs in a male-dominated, virally suppressed HIV population.

## Key findings

- PLWH on PIs had higher IL-6 levels compared to those on INSTIs.
- A greater proportion of INSTI users had normal LBP levels.
- PIs were associated with higher cholesterol levels compared to INSTIs.

## Abstract

Background and Objectives: The success of combined antiretroviral therapy (cART) has led to a dramatic improvement in the life expectancy of people living with HIV (PLWH). However, there has been an observed increase in cardiometabolic, bone, renal, hepatic, and neurocognitive manifestations, as well as neoplasms, known as serious non-AIDS events/SNAEs, compared to the general population of corresponding age. This increase is linked to a harmful phenomenon called inflammaging/immunosenescence, which is driven by chronic immune activation and intestinal bacterial translocation. In this study, we examined immunological and metabolic parameters in individuals receiving current cART. Materials and Methods: The study was conducted at Laiko General Hospital in Athens, Greece. Plasma concentrations of sCD14, IL-6, SuPAR, I-FABP, and LBP were measured in virally suppressed PLWH under cART with at least 350 CD4 lymphocytes/μL. We compared these levels between PLWH receiving integrase strand transfer inhibitors (INSTIs) and protease inhibitors (PIs) and attempted to correlate them with chronic immune activation and metabolic parameters. Results: Data from 28 PLWH were analyzed, with a mean age of 52 and 93% being males. Among the two comparison groups, IL-6 levels were higher in the PIs group (5.65 vs. 7.11 pg/mL, p = 0.03). No statistically significant differences were found in the other measured parameters. A greater proportion of PLWH under INSTIs had normal-range LBP (33% vs. 0%, p = 0.04). When using inverse probability of treatment weighting, no statistically significant differences in the measured parameters were found between the two groups (sCD14 p = 0.511, IL-6 p = 0.383, SuPAR p = 0.793, I-FABP p = 0.868, and LBP p = 0.663). Glucose levels were found to increase after viral suppression in the entire sample (92 mg/dL vs. 98 mg/dL, p = 0.009). Total (191 mg/dL vs. 222 mg/dL, p = 0.005) and LDL cholesterol (104 mg/dL vs. 140 mg/dL, p = 0.002) levels were higher in the PIs group. No significant differences were observed in liver and renal function tests. Conclusions: Further investigation is warranted for PLWH on cART-containing INSTI regimens to explore potential reductions in chronic immune activation and intestinal bacterial translocation.

## Linked entities

- **Proteins:** Scd1_1 (acyl-CoA Delta-9 desaturase), IL6 (interleukin 6), Su(par) (Suppressor of paralog), FABP2 (fatty acid binding protein 2), LBP (lipopolysaccharide binding protein)

## Full-text entities

- **Genes:** FABP2 (fatty acid binding protein 2) [NCBI Gene 2169] {aka FABPI, I-FABP}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, LBP (lipopolysaccharide binding protein) [NCBI Gene 3929] {aka BPIFD2}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}
- **Diseases:** Chronic Immune Activation (MESH:D006521), neoplasms (MESH:D009369), HIV (MESH:D015658), bone, renal, hepatic, and neurocognitive manifestations (MESH:D001847), AIDS (MESH:D000163)
- **Chemicals:** Glucose (MESH:D005947), cholesterol (MESH:D002784), Inhibitors (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10890512/full.md

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Source: https://tomesphere.com/paper/PMC10890512