# PD-L1 expression in squamous cervical carcinomas of Mozambican women living with or without HIV

**Authors:** Lucília Lovane, Satish Tulsidás, Carla Carrilho, Christina Karlsson

PMC · DOI: 10.1038/s41598-024-63595-7 · Scientific Reports · 2024-06-05

## TL;DR

This study examines PD-L1 expression in cervical cancer patients in Mozambique, including those living with HIV, to assess potential for immunotherapy.

## Contribution

The study provides insights into PD-L1 expression in HIV-positive cervical cancer patients, a group often excluded from clinical trials.

## Key findings

- PD-L1 was positive in 20.1% of cases using TPS and 26.3% using CPS.
- HIV status did not significantly affect PD-L1 expression levels.
- CD8 expression influenced only CPS status.

## Abstract

Programmed death-ligand 1 (PD-L1) is overexpressed in squamous cervical cancer (SCC) and can be used for targeted immunotherapy. The highest mortality rates of SCC are reported in sub-Saharan Africa, where Human immunodeficiency virus (HIV) prevalence is high. In Mozambique most SCC patients present at advanced stages. Thus, there is a need to introduce new treatment options. However, immunocompromised patients were frequently excluded in previous clinical trials. Our aim was to determine if PD-L1 expression in SCC is as prevalent among women living with HIV (WLWH) as among other patients. 575 SCC from Maputo Central Hospital were included. HIV status was available in 266 (46%) cases PD-L1 expression was scored through tumour proportion score (TPS) and combined positive score (CPS). PD-L1 was positive in 20.1% of the cases (n = 110), TPS (score ≥ 25%) and in 26.3% (n = 144), CPS (score ≥ 1). Stratifying according to the HIV status, WLWH were TPS positive in 16.7%, compared to 20.9%, p = 0.43, and concerning CPS 21.1% versus 28.7%, p = 0.19, respectively. PD-L1 status was not influenced by stage, Ki-67 or p16, CD8 expression influenced only CPS status. Our data indicates that the documented effect of PD-L1 therapy on SCC should be confirmed in randomized clinical trials in an HIV endemic milieu.

## Linked entities

- **Proteins:** CD274 (CD274 molecule), Mki67 (antigen identified by monoclonal antibody Ki 67), CDKN2A (cyclin dependent kinase inhibitor 2A), CD8A (CD8 subunit alpha)
- **Diseases:** squamous cervical cancer (MONDO:0006143), cervical cancer (MONDO:0002974)

## Full-text entities

- **Genes:** CDKN2A (cyclin dependent kinase inhibitor 2A) [NCBI Gene 1029] {aka ARF, CAI2, CDK4I, CDKN2, CMM2, INK4}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}
- **Diseases:** tumour (MESH:D009369), SCC (MESH:D018307), squamous cervical carcinomas (MESH:D065309)
- **Species:** Human immunodeficiency virus (species) [taxon 12721], Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC11153591/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11153591/full.md

## References

67 references — full list in the complete paper: https://tomesphere.com/paper/PMC11153591/full.md

---
Source: https://tomesphere.com/paper/PMC11153591