Systemic lupus erythematosus
View Patent ↗This document relates to methods and materials involved in diagnosing SLE. For example, this document relates to methods and materials involved in diagnosing SLE, diagnosing severe SLE, and assessing a mammal's susceptibility to develop severe SLE. For example, this document provides nucleic acid arrays that can be used to diagnose SLE in a mammal. Such arrays can allow clinicians to diagnose SLE based on a simultaneous determination of the expression levels of many genes that are differentially expressed in SLE patients as compared to healthy controls. In addition, methods and materials for assessing SLE activity, determining the likelihood of experiencing active SLE, and detecting SLE treatment effectiveness are provided herein.
1. A method for assessing effectiveness of a treatment for systemic lupus erythematosus, said method comprising:
providing a biological sample from a mammal having systemic lupus erythematosus disease and having received a treatment for said systemic lupus erythematosus disease, and
measuring gene expression in said sample to determine whether or not said mammal contains cells having an IFN signature 1 to a level less than that observed prior to said treatment,
wherein said IFN signature 1 comprises an expression profile comprising at least 60 percent of the genes listed in Table 5, and wherein the presence of said cells indicates that said treatment is effective.
2. The method of claim 1 , wherein said mammal is a human.
3. The method of claim 1 , wherein said cells are peripheral blood mononuclear cells.
4. The method of claim 1 , wherein said treatment comprises an anti-IFN treatment.
5. The method of claim 4 , wherein said anti-IFN treatment comprises a humanized anti-IFN antibody.
6. The method of claim 1 , wherein said treatment comprises hydroxychloroquinone.
7. The method of claim 1 , wherein said treatment comprises steroids.
8. The method of claim 1 , wherein said treatment comprises an immunosuppressive drug.
9. The method of claim 1 , wherein said biological sample comprises blood.
10. The method of claim 1 , wherein said biological sample comprises serum.
11. The method of claim 1 , wherein said biological sample comprises plasma.
12. The method of claim 1 , wherein said biological sample comprises peripheral blood mononuclear cells.
13. The method of claim 1 , wherein said biological sample comprises urine.
14. The method of claim 1 , wherein said biological sample comprises total white blood cells, lymph node cells, spleen cells, or tonsil cells.