Persistent T cell unresponsiveness associated with chronic visceral leishmaniasis in HIV-coinfected patients

Author:

de Vrij NickyORCID,Pollmann JuliaORCID,Rezende Antonio M.ORCID,Ibarra-Meneses Ana V.,Pham Thao-Thy,Hailemichael WasihunORCID,Kassa Mekibib,Bogale Tadfe,Melkamu Roma,Yeshanew Arega,Mohammed Rezika,Diro ErmiasORCID,Maes Ilse,Domagalska Malgorzata A.ORCID,Landuyt Hanne,Vogt Florian,van Henten SaskiaORCID,Laukens KrisORCID,Cuypers BartORCID,Meysman PieterORCID,Beyene Hailemariam,Sisay Kasaye,Kibret Aderajew,Mersha Dagnew,Ritmeijer Koert,van Griensven Johan,Adriaensen WimORCID

Abstract

AbstractA large proportion of HIV-coinfected visceral leishmaniasis (VL-HIV) patients exhibit chronic disease with frequent VL recurrence. However, knowledge on immunological determinants underlying the disease course is scarce. We longitudinally profiled the circulatory cellular immunity of an Ethiopian HIV cohort that included VL developers. We show that chronic VL-HIV patients exhibit high and persistent levels of TIGIT and PD-1 on CD8+/CD8- T cells, in addition to a lower frequency of IFN-γ+ TIGIT- CD8+/CD8- T cells, suggestive of impaired T cell functionality. At single T cell transcriptome and clonal resolution, the patients show CD4+ T cell anergy, characterised by a lack of T cell activation and lymphoproliferative response. These findings suggest that PD-1 and TIGIT play a pivotal role in VL-HIV chronicity, and may be further explored for patient risk stratification. Our findings provide a strong rationale for adjunctive immunotherapy for the treatment of chronic VL-HIV patients to break the recurrent disease cycle.

Publisher

Springer Science and Business Media LLC

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