1) The document discusses various potential therapies for human rabies that have been studied experimentally, including ketamine, ribavirin, interferon, and therapeutic coma. 2) Experiments in a mouse model found that ketamine did not provide any benefits such as reduced mortality or viral load, and it has also failed to help in at least 8 reported human rabies cases. 3) Similarly, the "Willoughby protocol" of inducing therapeutic coma has not proven effective and should not be continued without further study, as the risks may outweigh any unproven benefits. More research is needed to identify truly promising treatments.

1. Therapy of human rabies: lessons from experimental studies in a mouse model Alan C. Jackson, MD Courtney A. Scott, BSc James Owen, BSc Simon C. Weli, PhD John P. Rossiter, MB, PhD Departments of Medicine (Neurology) Microbiology and Immunology Centre for Neuroscience Studies Queen’s University, Kingston, ON, Canada

2. Medical complications of rabies multisystem organ failure respiratory failure, hyperventilation, aspiration pneumonia cardiac failure, arrhythmias gastrointestinal hemorrhage hyperthermia or hypothermia endocrine – SIADH, DI

3. Recovery from rabies 6-yr-old male from Ohio. Hattwick et al. Ann Intern Med (1972) 45-yr-old female from Argentina. Porras et al. Ann Intern Med (1976) 32-yr-old male lab worker from New York. Tillotson et al. MMWR (1977) 9-yr-old male from Mexico. Alvarez et al. Pediatr Infect Dis (1994) 6-yr-old female from India. Madhusudana et al. Int J Infect Dis (2002)

4. Clinical Infectious Diseases 36:60-63, 2003

5. Specific therapies rabies vaccine human rabies immune globulin (or mabs) ribavirin interferon-  ketamine role of combination therapy? Jackson et al.: Clinical Infectious Diseases 36:60-63, 2003

6. N Engl J Med 352:2508-14, 2005

7. Survival Case healthy 15-year-old in Wisconsin bitten by bat – probable bat rabies virus (no virus isolated, no antigen or RNA identified) antibodies on presentation (RFFIT 1:102) midazolam infusion to produce burst suppression pattern on EEG with supplemental phenobarbital IV ketamine infusion 2 mg/kg/hr antiviral therapy with ribavirin (IV) and amantadine N Engl J Med 352:2508-14, 2005

8. Survival Case Did specific therapy play important role in recovery? therapeutic coma?? ketamine? antiviral therapy? Attenuated bat rabies virus strain? Early antibody response Lack of detection of viral antigen and RNA, suggests that effective viral clearance was in progress

9. Ketamine dissociative anesthetic agent ketamine (1-2 mM) inhibits in vitro replication of rabies virus by inhibiting genome transcription with stereotaxic inoculation of fixed rabies virus into neostriatum of rats, ketamine 60 mg/kg IP q12h reduced infection in multiple brain regions (hippocampus, cerebral cortex, and thalamus) Lockhart et al. – Antiviral Chem Chemother 1991 and 1992 Antimicro Agents Chemother 1991

10. Journal of Virology 80:10270, 2006

11. Toluidine blue-stained plastic sections cerebral cortex – 48 hrs Mock-infected CVS-infected J Virol 80:10270, 2006

12. Trypan blue exclusion cerebral cortex – 72 hrs Mock-infected CVS-infected J Virol 80:10270, 2006

13. Trypan Blue Staining Cerebral Cortex Hippocampus J Virol 80:10270, 2006

14. Effects of 125 μ M ketamine on viability of cortical neurons in CVS infection J Virol 80:10270, 2006

16. Cumulative mortality ketamine 60 mg IP q12h or vehicle intracerebral footpad log rank test p= 0.50 log rank test p= 0.53 J Virol 80:10270, 2006

17. Therapy with Ketamine Ketamine did not: reduce mortality attenuate the clinical neurologic illness or prolong survival reduce viral spread or the number of infected neurons reduce the amount of infectious virus reduce neuronal apoptosis after intracerebral inoculation

18. Lancet Neurology 3:744, 2004 multiple sclerosis spinal cord injury Parkinson’s disease Huntington’s disease amyotrophic lateral sclerosis viral diseases of CNS – reovirus, SIV, Sindbis v.

19. Journal of Virology 81:6248, 2007

20. log rank test p=0.003 J Virol 81:6248, 2007

21. Summary Therapy with minocycline (50 mg/kg/d) was associated with more severe neurologic disease and higher mortality than with vehicle in rabies virus – infected mice. The number of rabies virus-infected neurons was similar with vehicle and minocycline. Neuronal apoptosis was more marked in infected mice that received vehicle than minocycline (minocycline was anti-apoptotic ). There were smaller numbers of CD3 positive cells in the brainstem of mice that received minocycline than vehicle, indicating an anti-inflammatory effect of the drug. J Virol 81:6248, 2007

22. Conclusions Therapy of rabies with minocycline in an experimental mouse model did not provide neuroprotection and aggravated the neurological disease. Caution should be taken before using minocycline for empirical therapy of rabies or other viral encephalitis in humans before more experimental data become available.

23. Therapeutic approach similar to the Willoughby protocol has been unsuccessful in at least 8 cases: United States – 3 (TX, IN, CA) Canada (Alberta) Germany – 2 India Thailand

24. Conclusions: Ketamine Lack of efficacy of ketamine in about 8 human cases since the Milwaukee case Lack of efficacy of ketamine in primary neuronal cultures and in vivo in mice at 120mg/kg/d More experimental evidence is needed that supports the use of ketamine in rabies virus infection before recommending its use for the therapy of human rabies.

25. Therapeutic coma useful for therapy of status epilepticus efficacy in other neurologic disorders is unproven no experimental evidence of efficacy in rabies or any other infectious disease potential serious adverse effects lack of effective neuroprotective agents even in common acute neurologic disorders (e.g., stroke), despite numerous clinical trials no scientific rationale for use in rabies does not work risks outweigh benefits should not be used for human rabies

26. Willoughby protocol Multiple failures of the protocol in developed and developing countries. It is now highly questionable that therapy using this protocol was directly responsible for the favorable outcome. This protocol should not be repeated indefinitely. Experimental work should be performed in cell culture and in animal models to identify promising therapeutic agents. New approaches should be taken for future rabies patients.

27. Acknowledgments Queen’s University Violet E. Powell Fund