Stimulation of a nerve supplying the spleen
Stimulation of neural activity in a nerve supplying the spleen, wherein the nerve is associated with a neurovascular bundle, can modulate pro- and anti-inflammatory molecules levels, thereby reducing inflammation and providing ways of treating inflammatory disorders. The invention provides improved ways of treating inflammatory disorders which minimize off-target effects.
1. A system for stimulating neural activity of a nerve supplying a spleen,
wherein the nerve is associated with a neurovascular bundle, the system comprising:
at least one electrode configured to be in signaling contact with the nerve supplying the spleen, wherein the nerve is associated with the neurovascular bundle; and
at least one controller electrically coupled to the at least one electrode, the at least one
controller configured to control operation of the at least one electrode to apply an electrical signal having a charge density to the nerve, wherein the charge density per phase applied to the nerve supplying the spleen by the electrical signal is >40 μC per cm2 per phase and < 150 μC per cm2 per phase, wherein the electrical signal produces an improvement in a physiological parameter in a subject, wherein the improvement in the physiological parameter is one or more of the group consisting of: a reduction in pro-inflammatory cytokines, an increase in anti-inflammatory cytokines and/or pro-resolving mediators, an increase in catecholamines, changes in immune cell population or immune cell surface co-stimulatory molecules, a reduction in factors involved in an inflammation cascade, and/or a reduction in immune response mediators.
2. The system of claim 1 , wherein the electrical signal comprises a pulse train comprising a plurality of pulses.
3. A method of determining whether a neural interface is correctly placed
in signaling contact with a nerve supplying a spleen, wherein the nerve is associated with a neurovascular bundle, the method comprising:
providing the system of claim 1 ;
positioning the neural interface in signaling contact with the nerve supplying the spleen, wherein the nerve is associated with the neurovascular bundle;
controlling the operation of the at least one electrode with the at least one controller to apply an electrical signal to the nerve;
determining at least one of: blood flowrate in the spleen, blood flow rate in a splenic artery, blood flowrate in a splenic vein, spleen volume, neural activity in the nerve, or impedance of the at least one electrode; and
indicating to an operator that the neural interface had been placed correctly in signaling contact with the nerve.
4. A method of reversibly stimulating neural activity in a nerve supplying
a spleen, wherein the nerve is associated with a neurovascular bundle, the method comprising:
providing the system of claim 1 ;
positioning the at least one electrode in signaling contact with the nerve supplying the spleen, wherein the nerve is associated with the neurovascular bundle; and
controlling operation of the at least one electrode with the at least one controller to apply an electrical signal to the nerve to stimulate neural activity.
5. The method of claim 4 , wherein the method is a treatment for an inflammatory disorder in a subject.
6. The method of claim 5 , wherein the inflammatory disorder is selected from the group of: arthritis, rheumatoid arthritis, osteoarthritis, psoriatic arthritis, Grave's disease, myasthenia gravis, thryoiditis, systemic lupus erythematosus, Goodpasture's syndrome, Behcets's syndrome, allograft rejection, graft-versus-host disease, ankylosing spondylitis, Berger's disease, diabetes including Type I diabetes, Reitier's syndrome, spondyloarthropathy, psoriasis, multiple sclerosis, Inflammatory Bowel Disease, Crohn's disease, Addison's disease, autoimmune mediated hair loss, alopecia areata, and ulcerative colitis.
7. The method of claim 5 , wherein the inflammatory disorder is selected from the group of: asthma, allergy, anaphylactic shock, immune complex disease, sepsis, septicemia, endotoxic shock, eosinophilic granuloma, granulomatosis, organ ischemia, reperfusion injury, organ necrosis, hay fever, cachexia, hyperexia, septic abortion, HIV infection, herpes infection, organ transplant rejection, disseminated bacteremia, Dengue fever, malaria, and sarcoidosis.
8. The method of claim 5 , wherein the inflammatory disorder is an autoimmune disorder.
9. The method of claim 8 , wherein the autoimmune disorder is selected from the group of: rheumatoid arthritis, osteoarthritis, psoriatic arthritis, spondyloarthropathy, ankylosing spondylitis, psoriasis, systemic lupus erythematosus (SLE), multiple sclerosis, Inflammatory Bowel Disease, Crohn's disease, ulcerative colitis, and sepsis.
10. The method of claim 8 , wherein the autoimmune disorder is systemic lupus erythematosus (SLE).
11. The method of claim 5 wherein the inflammatory disorder is rheumatoid arthritis.
12. The method of claim 5 wherein the treatment further comprises use of an anti-inflammatory medicine.
13. The method of claim 12 wherein the anti-inflammatory medicine is a nonsteroidal anti-inflammatory drug, a steroid, a 5ASA, a disease modifying-anti-inflammatory drug or a biological drug.
14. The method of claim 12 wherein the anti-inflammatory medicine is a nonsteroidal anti-inflammatory drug.
15. The method of claim 12 wherein the anti-inflammatory medicine is a steroid.
16. The method of claim 12 wherein the anti-inflammatory medicine is a 5 ASA.
17. The method of claim 12 wherein the anti-inflammatory medicine a disease modifying-anti-inflammatory drug (DMARDs).
18. The method of claim 17 wherein the DMARD is selected from the group consisting of azathioprine, methotrexate and cyclosporin.
19. The method of claim 17 wherein the DMARD is a Jak inhibitor.
20. The method of claim 12 wherein the anti-inflammatory medicine is a biological drug.
21. The method of claim 20 wherein the biological drug is infliximab or adalimumab.