Type I interferon drives dysfunction of a distinct CD8+ HLA-DRB1+ T cell subset in systemic lupus erythematosus

CD8+ HLA-DRB1+ T cells represent a cytotoxic yet dysfunctional effector memory population expanded in SLE. Type I IFN drives this paradoxical state by promoting exhaustion and impaired degranulation, highlighting a potential therapeutic axis in SLE.

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Publication Details

Journal
medRxiv
Published
2026-01-03
DOI
https://doi.org/10.64898/2026.01.02.26343348
Primary Topic
Systemic Lupus Erythematosus Research
Type
article
Field-Weighted Citation Impact
0.00
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article

Type I interferon drives dysfunction of a distinct CD8+ HLA-DRB1+ T cell subset in systemic lupus erythematosus

Amr H. Sawalha, H. Long, Elio G. Carmona, Mikhail Dozmorov
medRxiv
Systemic Lupus Erythematosus Research
article

Type I interferon drives dysfunction of a distinct CD8+ HLA-DRB1+ T cell subset in systemic lupus erythematosus

Amr H. Sawalha, H. Long, Elio G. Carmona, Mikhail Dozmorov
article en

Abstract

CD8+ HLA-DRB1+ T cells represent a cytotoxic yet dysfunctional effector memory population expanded in SLE. Type I IFN drives this paradoxical state by promoting exhaustion and impaired degranulation, highlighting a potential therapeutic axis in SLE.

medRxiv
Central South University (CN), University of Pittsburgh (US), Virginia Commonwealth University (US), Children's Hospital of Pittsburgh (US), Xiangya Hospital Central South University (CN)
Openalex Percentile: Top 98%
Systemic Lupus Erythematosus Research
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