Abstract

Worldwide, more than 200 million people are infected with filariae which can cause severe symptoms leading to reduced quality of life and contribute to disability-adjusted life years (DALYs). In particular, lymphatic filariasis (LF) caused by Wuchereria bancrofti can lead to lymphedema (LE) and consequently presents a serious health problem. To understand why only a fraction of the infected individuals develop pathology, it is essential to understand how filariae regulate host immunity. The central role of T cells for immunity against filariae has been shown in several studies. However, there is little knowledge about T cell exhaustion, which causes T cell dysfunction and impaired immune responses, in this group of individuals. Recently, we showed that LE patients from Ghana harbor distinct patterns of exhausted effector and memory CD8+ T cell subsets. Based on these findings, we now characterized CD4+ T cell subsets from the same Ghanaian patient cohort by analyzing distinct markers within a 13-colour flow cytometry panel. We revealed that LE patients had increased frequencies of CD4+ T cells expressing exhaustion-associated receptors such as KLRG-1, TIM-3 and PD-1 compared to healthy endemic normal and W. bancrofti-infected individuals. Moreover, CD4+ T cells in LE patients were characterized by distinct co-expression patterns of inhibitory receptors. Collectively with the previous findings on CD8+ T cell exhaustion patterns, the data shown here demonstrates that filarial LE patients harbor distinct subsets of exhausted T cells. Thus, T cell exhaustion patterns in LE patients need attention especially in regards to susceptibility of concomitant infections and should be taken into consideration for LE management measures.

Highlights

  • The Global Programme to Eliminate Lymphatic Filariasis (GPELF), implemented more than 20 years ago, includes mass drug administration (MDA) and vector control programmes

  • By using advanced flow cytometry to explore the expression of these exhaustion-associated markers on T cells, we recently showed that patients with LE due to lymphatic filariasis (LF) from Ghana harbour distinct exhaustion patterns of memory and effector CD8+ T cell subsets compared to W. bancrofti-infected individuals and healthy endemic controls (Horn et al, 2021)

  • Due to our recent findings that Ghanaian individuals presenting LF-induced LE are characterized by distinct patterns of exhausted effector and memory CD8+ T cell subsets (Horn et al, 2021), we investigated whether CD4+ T cell subsets were affected

Read more

Summary

INTRODUCTION

The Global Programme to Eliminate Lymphatic Filariasis (GPELF), implemented more than 20 years ago, includes mass drug administration (MDA) and vector control programmes. Despite the tightly controlled immune-regulation, individuals with LF can develop severe symptoms like hydrocele or lymphedema (LE) as well as adenolymphangitis (ADL) attacks (World Health Organization, 2020; World Health Organisation 2021) This often leads to reduced quality of life and increased disability-adjusted life years (DALYs), financial losses, and social separation due to the stigmatization (Gyapong et al, 1996; van 't Noordende et al, 2020; Asiedu et al, 2021). By using advanced flow cytometry to explore the expression of these exhaustion-associated markers on T cells, we recently showed that patients with LE due to LF from Ghana harbour distinct exhaustion patterns of memory and effector CD8+ T cell subsets compared to W. bancrofti-infected individuals and healthy endemic controls (Horn et al, 2021). We further investigated the exhaustion patterns on CD4+ T cell subsets from W. bancrofti-infected individuals, healthy controls and individuals that suffer from LE and revealed an increased expression of these markers on CD4+ T cells from patients presenting clinical pathology

METHODS
RESULTS
DISCUSSION
ETHICS STATEMENT
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.