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Updated: May 14, 2026

The bm12 Inducible Model of Systemic Lupus Erythematosus (SLE) in C57BL/6 Mice
Published on: November 1, 2015
NK cells dysfunction in systemic lupus erythematosus: relation to disease activity
Ana Henriques1, Luís Teixeira, Luís Inês
1Centro do Sangue e da Transplantação de Coimbra | Instituto Português do Sangue e da Transplantação, Edifício São Jerónimo. 4 Piso, Praceta Mota Pinto, 3001-301 Coimbra, Portugal.
Natural killer (NK) cells play a role in autoimmune diseases like systemic lupus erythematosus (SLE). This study found unique changes in NK cell subsets in SLE patients, particularly those with active disease, suggesting a potential impact on disease progression.
Area of Science:
- Immunology
- Autoimmune Diseases
Background:
- Natural killer (NK) cells modulate autoimmune diseases through cytotoxic and cytokine functions.
- The specific role of NK cells in systemic lupus erythematosus (SLE) pathogenesis requires further investigation.
Purpose of the Study:
- To analyze the immunophenotypic and functional characteristics of major NK cell subsets in SLE patients.
- To correlate these characteristics with SLE disease activity.
Main Methods:
- Flow cytometry was used to analyze peripheral blood samples from 44 SLE patients (active and inactive) and 30 controls.
- NK cell subsets were evaluated based on CXCR3, CD57, granzyme B, perforin expression, and IFN-γ and TNF-α production after activation.
Main Results:
- SLE patients, especially those with active disease, showed decreased circulating NK cell numbers.
- Active SLE was linked to reduced CXCR3 expression on NK cells and lower TNF-α production by CD56(bright) and CD56(dim) subsets.
- Increased IFN-γ expression was observed in CD56(bright) NK cells in both SLE groups.
Conclusions:
- NK cell subsets display distinct phenotypic and functional alterations in SLE patients.
- These changes are more pronounced in active SLE and may influence disease outcomes.
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