by Stephan Wiegand, Dresden University of Technology

Single-cell RNA sequencing of PBMCs of patient 3 and controls. (A) Uniform manifold approximation and projection (UMAP) of integrated data from patient 3 and two controls, assigned to 11 cell (sub)types: B cells (B); monocytes (mono: CD16+, CD14+, and CD14+/CD16+); T cells (T: CD8⁺ and CD4⁺, proliferating, central memory-like); natural killer cells (NK); conventional dendritic cells (cDC); plasmacytoid dendritic cells (pDC). (B) Dot plot displaying the expression of IFN-stimulated genes across cell types. (C) Violin- and box- plots displaying cytotoxic, exhaustion, and IFN signature expression levels in CD8⁺ T cells. (D) Violin plots displaying gene set expression levels of the indicated GO terms in the indicated cell types. Credit: Science Immunology (2024). DOI: 10.1126/sciimmunol.adi9769

Systemic lupus erythematosus (SLE) is an autoimmune disease, in which the immune system that normally protects the body from invading microbes, turns against the body's own cells. This autoimmune attack can affect any organ and patients commonly develop skin rashes, joint inflammation, blood clots, kidney failure, heart disease, fatigue and psychiatric problems. To date, there is no cure for SLE and patients are treated with immunosuppressing drugs with considerable side effects.

A group of researchers led by Min Ae Lee-Kirsch from the Department of Pediatrics, Medical Faculty, TUD Dresden University of Technology (Germany), studied four patients from two families who developed symptoms of SLE in the first years of life. As familial occurrence of SLE in young children is highly unusual, her team searched for a primary genetic cause and found a mutation in the UNC93B1 gene in all affected family members. The research is published in Science Immunology.

UNC93B1 is a membrane-spanning structural protein required for maturation and trafficking of a group of receptors that play an important role in the defense against viral infections. These receptors recognize the nucleic acid component of the virus and activate type I interferons, which instruct cells to fight a viral infection. However, nucleic acids, such as DNA and RNA, are not only found in viruses, but are also present in every cell of the human body. This means that the immune system must be capable of discriminating foreign from self nucleic acids.

The identified UNC93B1 mutations lead to selective overactivation of TLR7, one of the UNC93B1-regulated receptors that specifically recognizes RNA, leading to erroneous recognition of self RNA with uncontrolled overproduction of type I interferon. This results in an immune attack on normal cells, which then triggers inflammation.

Moreover, this also stimulates the survival of self-reactive B cells that produce autoantibodies directed against the body's own cells, fueling the autoimmune attack. These findings demonstrate that UNC93B1 controls the activity of specific nucleic acid receptors, such as TLR7, thereby preventing autoimmunity.

Remarkably, people lacking functional UNC93B1 are prone to viral infections with a severe course, such as herpes simplex virus encephalitis and severe COVID-19, highlighting the essential role of UNC93B1 for a healthy immune system.

The findings of this study are also of clinical relevance regarding the development of novel targeted therapies for patients with common forms of SLE, who often show signs of overactivation of the TLR7 pathway.

Professor Lee-Kirsch says, "Our study demonstrates a direct causal link between an overactive UNC93B1/TLR7 axis and lupus pathogenesis and indicates that blocking overactive TLR7 might be therapeutically effective. As such, our findings are expected to accelerate further development of TLR7 inhibitors for patients with SLE and related autoimmune diseases."

More information: Christine Wolf et al, UNC93B1 variants underlie TLR7-dependent autoimmunity, Science Immunology (2024). DOI: 10.1126/sciimmunol.adi9769

Journal information: Science Immunology 

Provided by Dresden University of Technology