Sustained NPSLE-like phenotype in the absence of systemic lupus-like disease in TLR7-deficient B6.Nba2 mice

While systemic lupus-like disease in the B6.Nba2 mouse model is dependent on TLR7, NPSLE development is not and may be influenced by TLR4 and TLR9 signaling. Thus, there may be separate mechanisms driving peripheral SLE compared to NPSLE with possible implications for pharmacologic management.

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Publication Details

Journal
Brain Behavior and Immunity
Published
2025-04-15
DOI
https://doi.org/10.1016/j.bbi.2025.04.017
Citations
3
Primary Topic
Immunodeficiency and Autoimmune Disorders
Type
article
Field-Weighted Citation Impact
2.39

Funders

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article

Sustained NPSLE-like phenotype in the absence of systemic lupus-like disease in TLR7-deficient B6.Nba2 mice

James Sullivan, Audrey Kwun, Gabrielle M. Mey, S Liu et al.
3 citations
Brain Behavior and Immunity
Immunodeficiency and Autoimmune Disorders
2.39
article

Sustained NPSLE-like phenotype in the absence of systemic lupus-like disease in TLR7-deficient B6.Nba2 mice

James Sullivan, Audrey Kwun, Gabrielle M. Mey, S Liu, Tara M. DeSilva, John Shelestak, Trine N. Jørgensen, Katharine Merritt
article en
3 citations

Abstract

While systemic lupus-like disease in the B6.Nba2 mouse model is dependent on TLR7, NPSLE development is not and may be influenced by TLR4 and TLR9 signaling. Thus, there may be separate mechanisms driving peripheral SLE compared to NPSLE with possible implications for pharmacologic management.

Brain Behavior and ImmunityVol. 128
Cleveland Clinic (US), Cleveland Foundation (US), Cleveland Clinic Lerner College of Medicine (US)
U.S. Department of Defense, National Institute of Allergy and Infectious Diseases
Openalex Percentile: Top 12%
Immunodeficiency and Autoimmune Disorders
2.39
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