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•   ‘HERPES’   – most common viral infection in oral
  cavity .
• The term ‘herpes simplex’ –herpes labialis(cold
  sores) & herpes progenital(genital herpes), fever
  blisters
• Herpes viridae family includes
I. HSV-1
II. HSV-2
III. Varicella zoster
IV. Epstein –Barr virus
V. Cytomegalovirus
VI. HHV-6
VII. HHV 7
VIII. HHV 8
IX.Herpes virus simian
• HSV-1 (oral herpes) - permanent infection ,
  very infectious
• Oral herpes simplex virus infection(HSV 1) –
  herpes simplex virus(HSV)
Structure:
• VIRION - > double stranded - DNA genome
,icosahedral protein cage - capsid ,lipid bilayer –
envelope ,envelope joined to capsid – tegument .
•HSV1 & HSV2 – 74 genes within genome .
• DNA core – control replication & infectivity of the
virus .
• Ballooning degeneration, contain intranuclear
  inclusions known as Lipschitiz bodies.
• Cytoplasm of the infected cell forms giant cells
  .
 Types of HSV –> HSV 1 - >physical contact in oral
  cavity .
•                     HSV 2 ->’new epidemic
  disease’ -contracted             through sexual
  contact .
 HSV 1 &2 occurs as:
1. Primary infection
2. Recurrent infection – milder than primary infection
Susceptible host
                                                   Virus

      primary infection
                                      Recurrent manifestation



Clinical   Subclinical
disease 1% disease 99%
                                              Excitants



          Carries (70% -80% of population)
          Antibodies & virus presist
•   Primary infection
•   Incubation period –> 1-26 days.
•    Prodromal Symptoms –( fever ,headache ,loss of
    appetite , tiredness , irritation .)
•   Appearance- group of small red bumps that blister,
    begin to dry , form yellow crust - preceded by itching
    &burning -10 to14 days
•   Red swollen , bleeding gums or sore throat and
    enlarged lymph node
•   Gingivastomatitis - in infant from mother
•   HSV -latent infection in trigeminal ganglion
• Severe in immunodeficient & neonates .
• Complication – meningoencephalitis and
  keratoconjuctivis
• Impetigo



• Aphthous ulcers




• Hand foot & mouth disease
 Clinical
 Lab test:
• Smear test
• Tissue culture
• Biopsy
 Antiviral
• Acyclovir -> orally- 400mg -800mg .
•                  injection-10mg/kg body weight .
• Famciclovir -> 250mg & 500mg .
• Valacyclovir -> 500mg & 1gm
 Antibiotic- (secondary infection
 like bacteria )
• Always keep the infected area
  dry
VIRAL THYMIDINE KINASE




CELLULAR KINASE
ACYCLOVIR
• Used to treat herpes group of virus
• Pharmacokinetics – poor biocompatibility 20%
•                            widely distributed
• Excreted- mainly in urine ,renal impairment dose
  reduction
• Effective in normal as well as deficient immune
  status
• Adverse effect – tiredness ,rashes ,hypotension
• Toxicity ->
1. Decrease in Glomerular filtration rate &produces
   reversible neurological manifestation to higher
   doses
FAMCYCLOVIR
• Ester prodrug of guanine nucleoside –penciclovir
• Good oral biocompatibility ,prolonged intracellular t
  ½ active triphosphate metabolite
• Treat ->Herpes zoster(shingles)->500mg every 8
  hours                  HSV2 ->250mg 5 days
   Herpes labialis (immunodeficient patients)-
  >1500mg oral dose
• Toxicity is more in famciclovir especially in bone
  marrow
VALACYCLOVIR
• VALACYCLOVIR –herpes simplex
• Prodrug ->esterases ->aminoacid valine->via
  hepatic first pass metabolism,greater
  biocompatibility(55%) than acyclovir(10-20%)
• Dosage –Valtrex ->500mg & 1mg /day
• Adverse effect –Vertigo ,edema ,arthralgia
• Avoid touching the affected area .




•   Vaccines – under research




• HSV 2 – condoms can be used
Oral herpes paper presentation
Oral herpes paper presentation

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Oral herpes paper presentation

  • 1.
  • 2. ‘HERPES’ – most common viral infection in oral cavity . • The term ‘herpes simplex’ –herpes labialis(cold sores) & herpes progenital(genital herpes), fever blisters
  • 3. • Herpes viridae family includes I. HSV-1 II. HSV-2 III. Varicella zoster IV. Epstein –Barr virus V. Cytomegalovirus VI. HHV-6 VII. HHV 7 VIII. HHV 8 IX.Herpes virus simian
  • 4. • HSV-1 (oral herpes) - permanent infection , very infectious • Oral herpes simplex virus infection(HSV 1) – herpes simplex virus(HSV)
  • 5. Structure: • VIRION - > double stranded - DNA genome ,icosahedral protein cage - capsid ,lipid bilayer – envelope ,envelope joined to capsid – tegument . •HSV1 & HSV2 – 74 genes within genome . • DNA core – control replication & infectivity of the virus .
  • 6. • Ballooning degeneration, contain intranuclear inclusions known as Lipschitiz bodies. • Cytoplasm of the infected cell forms giant cells .
  • 7.  Types of HSV –> HSV 1 - >physical contact in oral cavity . • HSV 2 ->’new epidemic disease’ -contracted through sexual contact .  HSV 1 &2 occurs as: 1. Primary infection 2. Recurrent infection – milder than primary infection
  • 8. Susceptible host Virus primary infection Recurrent manifestation Clinical Subclinical disease 1% disease 99% Excitants Carries (70% -80% of population) Antibodies & virus presist
  • 9. Primary infection • Incubation period –> 1-26 days. • Prodromal Symptoms –( fever ,headache ,loss of appetite , tiredness , irritation .) • Appearance- group of small red bumps that blister, begin to dry , form yellow crust - preceded by itching &burning -10 to14 days • Red swollen , bleeding gums or sore throat and enlarged lymph node • Gingivastomatitis - in infant from mother • HSV -latent infection in trigeminal ganglion
  • 10. • Severe in immunodeficient & neonates . • Complication – meningoencephalitis and keratoconjuctivis
  • 11. • Impetigo • Aphthous ulcers • Hand foot & mouth disease
  • 12.  Clinical  Lab test: • Smear test • Tissue culture • Biopsy
  • 13.  Antiviral • Acyclovir -> orally- 400mg -800mg . • injection-10mg/kg body weight . • Famciclovir -> 250mg & 500mg . • Valacyclovir -> 500mg & 1gm  Antibiotic- (secondary infection  like bacteria ) • Always keep the infected area dry
  • 15. ACYCLOVIR • Used to treat herpes group of virus • Pharmacokinetics – poor biocompatibility 20% • widely distributed • Excreted- mainly in urine ,renal impairment dose reduction • Effective in normal as well as deficient immune status • Adverse effect – tiredness ,rashes ,hypotension • Toxicity -> 1. Decrease in Glomerular filtration rate &produces reversible neurological manifestation to higher doses
  • 16. FAMCYCLOVIR • Ester prodrug of guanine nucleoside –penciclovir • Good oral biocompatibility ,prolonged intracellular t ½ active triphosphate metabolite • Treat ->Herpes zoster(shingles)->500mg every 8 hours HSV2 ->250mg 5 days Herpes labialis (immunodeficient patients)- >1500mg oral dose • Toxicity is more in famciclovir especially in bone marrow
  • 17. VALACYCLOVIR • VALACYCLOVIR –herpes simplex • Prodrug ->esterases ->aminoacid valine->via hepatic first pass metabolism,greater biocompatibility(55%) than acyclovir(10-20%) • Dosage –Valtrex ->500mg & 1mg /day • Adverse effect –Vertigo ,edema ,arthralgia
  • 18. • Avoid touching the affected area . • Vaccines – under research • HSV 2 – condoms can be used