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EBOLA: FACTS AND MEASURES
BY: SHUBHAM DEY
ROLL NO: 18901915090
REG. NO.: 151890210090
GUIDED BY: DIPESH CHAKRABORTY
CONTENTS
Epidemiology of Ebola
Pathophysiology of Ebola
Symptoms of Ebola
Therapeutics
New drugs in clinical research for Ebola
OBJECTIVES
 To learn more about Ebola, its threats, so that we can prepare ourselves for any eventuality.
 To learn about the steps undertaken around the world to prevent and curb further Ebola outbreaks.
 To delve further into the understanding of the deadly disease, which has taken a toll of more than millions of life
around the world.
EPIDEMIOLOGY
 The first case of filovirus haemorrhagic fever were reported in 1967 in Germany and the former
Yugoslavia, identified causative agent was Marburg virus.12
 An unknown causative agent was isolated from patients in the outbreak and named Ebola virus after a
small river in northwestern DRC.
PATHOPHYSIOLOGY
 Progression to severe disease occurs when the virus triggers expression of a host of pro-inflammatory
cytokines, including interferons; interleukins (ILs) such as IL-2, IL- 6, IL-8, and IL-10; interferon inducible
protein; and tumour necrosis factor α (TNF-α).8, 21, 24
 Thrombocytopenia is most commonly caused by loss of platelets from damaged tissue or more
generalised virus induced disseminated intravascular coagulation, where coagulation factors are
depleted.26
SYMPTOMS
 There are typically three phases of illness, starting with a few days of non-specific fever, headache, and
myalgia, followed by a gastrointestinal phase in which diarrhoea and vomiting, abdominal symptoms, and
dehydration are prominent.
 In the second week, the patient may recover or deteriorate, with a third phase of illness including
collapse, neurological manifestations, and bleeding, which is often fatal.38
THERAPEUTICS
MEDICAMENTS
1. Zmapp
2. TKM-Ebola
3. Favipiravir
MODE OF ACTION
1. A combination of three humanised monoclonal antibodies
targeted at three Ebola virus glycoprotein epitopes.
2. It consists of a combination of small interfering RNAs that target
Ebola virus RNA polymerase L, formulated with lipid
nanoparticle technology.
3. Formerly known as T-705, favipiravir selectively inhibits viral
RNA dependent RNA polymerase.
DRUGS IN CLINICAL TRIAL
Two experimental vaccines are currently undergoing trials.62 63
cAd3-ZEBOV is a chimpanzee derived adenovirus vector with
an Ebola virus gene inserted.76 Trials are under way in the United
Kingdom, United States, Switzerland, and some African
countries. rVSV-ZEBOV is an attenuated vesicular stomatitis
virus with one of its genes replaced by an Ebola virus gene.
Human trials have started in the US.
REFERENCES
 1. (12). Siegert R, Shu HL, Slenczka W, Peters D, Muller G. [On the etiology of an unknown human infection originating from monkeys] Dtsch Med
Wochenschr 1967; 92: 2341–43 (in German). Ebola haemorrhagic fever
 2. (8). Feldmann H, Geisbert TW. Ebola haemorrhagic fever. Lancet 2011;377:849-62. Ebola virus disease
 3. (21). Ramanan P, Shabman RS, Brown CS, Amarasinghe GK, Basler CF, Leung DW. Filoviral immune evasion mechanisms. Viruses
2011;3:1634-49. Ebola virus disease
 4. (24). Sanchez A, Lukwiya M, Bausch D, Mahanty S, Sanchez AJ, Wagoner KD, et al. Analysis of human peripheral blood samples from fatal and
nonfatal cases of Ebola (Sudan) hemorrhagic fever: cellular responses, virus load, and nitric oxide levels. J Virol 2004;78:10370-7. Ebola virus
disease
 5. (26). Leroy EM, Baize S, Volchkov VE, Fisher-Hoch SP, Georges-Courbot MC, Lansoud-Soukate J, et al. Human asymptomatic Ebola infection
and strong inflammatory response. Lancet 2000;355:2210-5. Ebola virus disease
 6. (38). Chertow DS, Kleine C, Edwards JK, Scaini R, Giuliani R, Sprecher A. Ebola virus disease in West Africa—clinical manifestations and
management. N Engl J Med 2014;371:2054-7. Ebola virus disease
 7. (62). Bishop BM. Potential and emerging treatment options for Ebola virus disease. Ann Pharmacother 2014; published online 20 Nov. Ebola
virus disease
REFERENCES
 8. (63). WHO. Potential Ebola therapies and vaccines. 2014. http://www.who.int/csr/resources/publications/ebola/potential-therapies-vaccines/en/.
Ebola virus disease
 9. (76). Ledgerwood JE, DeZure AD, Stanley DA, Novik L, Enama ME, Berkowitz NM, et al; the VRC 207 Study Team. Chimpanzee adenovirus
vector Ebola vaccine - preliminary report. N Engl J Med 2014; published online 26 Nov. doi:10.1056/NEJMoa1410863. Ebola virus disease
EBOLA.pptx

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EBOLA.pptx

  • 1. EBOLA: FACTS AND MEASURES BY: SHUBHAM DEY ROLL NO: 18901915090 REG. NO.: 151890210090 GUIDED BY: DIPESH CHAKRABORTY
  • 2. CONTENTS Epidemiology of Ebola Pathophysiology of Ebola Symptoms of Ebola Therapeutics New drugs in clinical research for Ebola
  • 3. OBJECTIVES  To learn more about Ebola, its threats, so that we can prepare ourselves for any eventuality.  To learn about the steps undertaken around the world to prevent and curb further Ebola outbreaks.  To delve further into the understanding of the deadly disease, which has taken a toll of more than millions of life around the world.
  • 4. EPIDEMIOLOGY  The first case of filovirus haemorrhagic fever were reported in 1967 in Germany and the former Yugoslavia, identified causative agent was Marburg virus.12  An unknown causative agent was isolated from patients in the outbreak and named Ebola virus after a small river in northwestern DRC.
  • 5. PATHOPHYSIOLOGY  Progression to severe disease occurs when the virus triggers expression of a host of pro-inflammatory cytokines, including interferons; interleukins (ILs) such as IL-2, IL- 6, IL-8, and IL-10; interferon inducible protein; and tumour necrosis factor α (TNF-α).8, 21, 24  Thrombocytopenia is most commonly caused by loss of platelets from damaged tissue or more generalised virus induced disseminated intravascular coagulation, where coagulation factors are depleted.26
  • 6. SYMPTOMS  There are typically three phases of illness, starting with a few days of non-specific fever, headache, and myalgia, followed by a gastrointestinal phase in which diarrhoea and vomiting, abdominal symptoms, and dehydration are prominent.  In the second week, the patient may recover or deteriorate, with a third phase of illness including collapse, neurological manifestations, and bleeding, which is often fatal.38
  • 7. THERAPEUTICS MEDICAMENTS 1. Zmapp 2. TKM-Ebola 3. Favipiravir MODE OF ACTION 1. A combination of three humanised monoclonal antibodies targeted at three Ebola virus glycoprotein epitopes. 2. It consists of a combination of small interfering RNAs that target Ebola virus RNA polymerase L, formulated with lipid nanoparticle technology. 3. Formerly known as T-705, favipiravir selectively inhibits viral RNA dependent RNA polymerase.
  • 8. DRUGS IN CLINICAL TRIAL Two experimental vaccines are currently undergoing trials.62 63 cAd3-ZEBOV is a chimpanzee derived adenovirus vector with an Ebola virus gene inserted.76 Trials are under way in the United Kingdom, United States, Switzerland, and some African countries. rVSV-ZEBOV is an attenuated vesicular stomatitis virus with one of its genes replaced by an Ebola virus gene. Human trials have started in the US.
  • 9. REFERENCES  1. (12). Siegert R, Shu HL, Slenczka W, Peters D, Muller G. [On the etiology of an unknown human infection originating from monkeys] Dtsch Med Wochenschr 1967; 92: 2341–43 (in German). Ebola haemorrhagic fever  2. (8). Feldmann H, Geisbert TW. Ebola haemorrhagic fever. Lancet 2011;377:849-62. Ebola virus disease  3. (21). Ramanan P, Shabman RS, Brown CS, Amarasinghe GK, Basler CF, Leung DW. Filoviral immune evasion mechanisms. Viruses 2011;3:1634-49. Ebola virus disease  4. (24). Sanchez A, Lukwiya M, Bausch D, Mahanty S, Sanchez AJ, Wagoner KD, et al. Analysis of human peripheral blood samples from fatal and nonfatal cases of Ebola (Sudan) hemorrhagic fever: cellular responses, virus load, and nitric oxide levels. J Virol 2004;78:10370-7. Ebola virus disease  5. (26). Leroy EM, Baize S, Volchkov VE, Fisher-Hoch SP, Georges-Courbot MC, Lansoud-Soukate J, et al. Human asymptomatic Ebola infection and strong inflammatory response. Lancet 2000;355:2210-5. Ebola virus disease  6. (38). Chertow DS, Kleine C, Edwards JK, Scaini R, Giuliani R, Sprecher A. Ebola virus disease in West Africa—clinical manifestations and management. N Engl J Med 2014;371:2054-7. Ebola virus disease  7. (62). Bishop BM. Potential and emerging treatment options for Ebola virus disease. Ann Pharmacother 2014; published online 20 Nov. Ebola virus disease
  • 10. REFERENCES  8. (63). WHO. Potential Ebola therapies and vaccines. 2014. http://www.who.int/csr/resources/publications/ebola/potential-therapies-vaccines/en/. Ebola virus disease  9. (76). Ledgerwood JE, DeZure AD, Stanley DA, Novik L, Enama ME, Berkowitz NM, et al; the VRC 207 Study Team. Chimpanzee adenovirus vector Ebola vaccine - preliminary report. N Engl J Med 2014; published online 26 Nov. doi:10.1056/NEJMoa1410863. Ebola virus disease