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Horn, Sacha; Ritter, Manuel; Arndts, Kathrin; Borrero-Wolff, Dennis; Wiszniewsky, Anna; Debrah, Linda Batsa; Debrah, Alexander Y.; Osei-Mensah, Jubin; Chachage, Mkunde; Hoerauf, Achim; Kroidl, Inge und Layland, Laura E. (2022): Filarial Lymphedema Patients Are Characterized by Exhausted CD4(+) T Cells. In: Frontiers in Cellular and Infection Microbiology, Bd. 11, 767306

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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.

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