HIV/AIDS
Introduction and Epidemiology
Mpondo B [MD., MMED., DTM&H]
What Is HIV?
 HIV (human immunodeficiency virus) is a
virus that attacks cells that help the body
fight infection, making a person more
vulnerable to other infections and
diseases
 If left untreated, HIV can lead to the
disease AIDS (acquired
immunodeficiency syndrome)
What Is AIDS?
 AIDS is the late stage of HIV infection that
occurs when the body’s immune system is
badly damaged because of the virus
 A person with HIV is considered to have
progressed to AIDS when:
• the number of their CD4 cells falls below 200 cells
per cubic millimeter of blood (200 cells/mm3 OR
• they develop one or more opportunistic infections
regardless of their CD4 count
History
 1981…First Reported Case of AIDS
 1982…First Use of “AIDS” Acronym
 1983…First reported case in Tanzania
 1984…Causative Agent Identified
 1985…First HIV Antibody Test
 1986…First Use of “HIV” Acronym
 1987…First Medication
HIV Origin
 Where did the virus come from?
HIV Introduction and Epidemiology.ppt,,,
Introduction
 Human immunodeficiency virus (HIV) is
a blood-borne, sexually transmissible
virus
 The virus is typically transmitted via
sexual intercourse, shared intravenous
drug paraphernalia, and mother-to-child
transmission (MTCT)
 The most common route of infection
varies from country to country and even
among cities
 Co-infection with other viruses that share
similar routes of transmission is common
HIV types
 Two distinct species of HIV
o HIV-1
o HIV-2
 Each is composed of multiple subtypes, or
clades
 All clades of HIV-1 tend to cause similar
disease, but the global distribution of the
clades differs
 HIV-1 is distributed worldwide, HIV-2 is
mainly present in West Africa
 Infection with HIV-2 causes slower
disease progression and is more
benign than infection with HIV-1
 HIV-1 is further divided into three
groups
o group M (main group, >98%)
o group O (outlier, <1%)
o group N (new, <1%)
 Group M is responsible for the majority
of HIV-1 infections worldwide
Subtypes /Clades
 HIV has subtypes: A-K (excluding I)
 Circulating recombinant forms (CRFs)
G
Source of infection
 HIV-1 probably originated from one or more
cross-species transfers from chimpanzees in
central Africa
 HIV-2 is closely related to viruses that infect
sooty mangabeys in western Africa
 Genetically, HIV-1 and HIV-2 are superficially
similar, but each contains unique genes and
its own distinct replication process
Virulence
 HIV-2:
o carries a slightly lower risk of transmission
o tends to progress more slowly to acquired
immune deficiency syndrome (AIDS)
 Persons infected with HIV-2 tend to have
lower viral load
Virology of HIV
 HIV-1 and HIV-2 are retroviruses in the
Retroviridae family, Lentivirus genus.
 They are:
o enveloped
o diploid
o single-stranded positive-sense RNA
Viral structure
 Basic components:
I. An outer membrane
II. A protein shell
III.Enzymes
IV.RNA
HIV Introduction and Epidemiology.ppt,,,
Viral entry into the cell &
lifecycle
Natural history of HIV
 Phases of HIV infection:
o Acute HIV Infection (acute
seroconversion)
o Chronic HIV Infection (asymptomatic
infection/clinical latency)
o AIDS
HIV Introduction and Epidemiology.ppt,,,
HIV disease progression
Normal progressors
Rapid progressors
Slow progressors
How does HIV cause AIDS????
 Any answers?
WHO HIV Clinical Staging
 FOUR Clinical stages:
• Stage 1 – Asymptomatic
• Stage 2 – Mild
• Stage 3 – Advanced
• Stage 4 – Severe
WHO Clinical Staging System (1)
 The WHO Clinical staging system is
based on clinical features that have
prognostic significance resulting in four
stages of disease progression
 WHO staging is done where HIV
infection is confirmed by HIV antibody or
virological markers
WHO Clinical Staging
Correlation Between WHO
Clinical Staging and CD4 Count
WHO 1
WHO 2
WHO 3
WHO 4
EPIDEMIOLOGY OF HIV
HIV Introduction and Epidemiology.ppt,,,
HIV Introduction and Epidemiology.ppt,,,
HIV Regional prevalence in
Tanzania (THIS 2016/2017)
Trend of HIV
Trend from 2000-2014
Racial, sexual, and age-related
differences in incidence:
 In the developed world, HIV infection is much
more common in males; in the developing
world in males and females
 Young adults tend to be at higher risk of
acquiring HIV
 Children may become infected by
transplacental transmission or by
breastfeeding
HIV transmission
 Risks of transmission:
o Unprotected sexual intercourse
o A large number of sexual partners
o Previous or current sexually transmitted infections (STIs)
o Sharing of intravenous (IV) drug paraphernalia
o Receipt of blood products
o Mucosal contact with infected blood or needle-stick
injuries
o Maternal HIV infection (for newborns, infants, and
children)
Risk per exposure
Vulnerable groups
 Men who have sex with men (MSM)
 Young men who have sex with men (YMSM)
 Sex workers
 People who inject drugs (PWID)
 Prisoners
 Women
 Transgender people
 Children
 Orphaned children
38

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HIV Introduction and Epidemiology.ppt,,,

  • 2. What Is HIV?  HIV (human immunodeficiency virus) is a virus that attacks cells that help the body fight infection, making a person more vulnerable to other infections and diseases  If left untreated, HIV can lead to the disease AIDS (acquired immunodeficiency syndrome)
  • 3. What Is AIDS?  AIDS is the late stage of HIV infection that occurs when the body’s immune system is badly damaged because of the virus  A person with HIV is considered to have progressed to AIDS when: • the number of their CD4 cells falls below 200 cells per cubic millimeter of blood (200 cells/mm3 OR • they develop one or more opportunistic infections regardless of their CD4 count
  • 4. History  1981…First Reported Case of AIDS  1982…First Use of “AIDS” Acronym  1983…First reported case in Tanzania  1984…Causative Agent Identified  1985…First HIV Antibody Test  1986…First Use of “HIV” Acronym  1987…First Medication
  • 5. HIV Origin  Where did the virus come from?
  • 7. Introduction  Human immunodeficiency virus (HIV) is a blood-borne, sexually transmissible virus  The virus is typically transmitted via sexual intercourse, shared intravenous drug paraphernalia, and mother-to-child transmission (MTCT)
  • 8.  The most common route of infection varies from country to country and even among cities  Co-infection with other viruses that share similar routes of transmission is common
  • 9. HIV types  Two distinct species of HIV o HIV-1 o HIV-2  Each is composed of multiple subtypes, or clades  All clades of HIV-1 tend to cause similar disease, but the global distribution of the clades differs
  • 10.  HIV-1 is distributed worldwide, HIV-2 is mainly present in West Africa  Infection with HIV-2 causes slower disease progression and is more benign than infection with HIV-1
  • 11.  HIV-1 is further divided into three groups o group M (main group, >98%) o group O (outlier, <1%) o group N (new, <1%)  Group M is responsible for the majority of HIV-1 infections worldwide
  • 12. Subtypes /Clades  HIV has subtypes: A-K (excluding I)  Circulating recombinant forms (CRFs)
  • 13. G
  • 14. Source of infection  HIV-1 probably originated from one or more cross-species transfers from chimpanzees in central Africa  HIV-2 is closely related to viruses that infect sooty mangabeys in western Africa  Genetically, HIV-1 and HIV-2 are superficially similar, but each contains unique genes and its own distinct replication process
  • 15. Virulence  HIV-2: o carries a slightly lower risk of transmission o tends to progress more slowly to acquired immune deficiency syndrome (AIDS)  Persons infected with HIV-2 tend to have lower viral load
  • 16. Virology of HIV  HIV-1 and HIV-2 are retroviruses in the Retroviridae family, Lentivirus genus.  They are: o enveloped o diploid o single-stranded positive-sense RNA
  • 17. Viral structure  Basic components: I. An outer membrane II. A protein shell III.Enzymes IV.RNA
  • 19. Viral entry into the cell & lifecycle
  • 20. Natural history of HIV  Phases of HIV infection: o Acute HIV Infection (acute seroconversion) o Chronic HIV Infection (asymptomatic infection/clinical latency) o AIDS
  • 22. HIV disease progression Normal progressors Rapid progressors Slow progressors
  • 23. How does HIV cause AIDS????  Any answers?
  • 24. WHO HIV Clinical Staging  FOUR Clinical stages: • Stage 1 – Asymptomatic • Stage 2 – Mild • Stage 3 – Advanced • Stage 4 – Severe
  • 25. WHO Clinical Staging System (1)  The WHO Clinical staging system is based on clinical features that have prognostic significance resulting in four stages of disease progression  WHO staging is done where HIV infection is confirmed by HIV antibody or virological markers
  • 27. Correlation Between WHO Clinical Staging and CD4 Count WHO 1 WHO 2 WHO 3 WHO 4
  • 31. HIV Regional prevalence in Tanzania (THIS 2016/2017)
  • 34. Racial, sexual, and age-related differences in incidence:  In the developed world, HIV infection is much more common in males; in the developing world in males and females  Young adults tend to be at higher risk of acquiring HIV  Children may become infected by transplacental transmission or by breastfeeding
  • 35. HIV transmission  Risks of transmission: o Unprotected sexual intercourse o A large number of sexual partners o Previous or current sexually transmitted infections (STIs) o Sharing of intravenous (IV) drug paraphernalia o Receipt of blood products o Mucosal contact with infected blood or needle-stick injuries o Maternal HIV infection (for newborns, infants, and children)
  • 37. Vulnerable groups  Men who have sex with men (MSM)  Young men who have sex with men (YMSM)  Sex workers  People who inject drugs (PWID)  Prisoners  Women  Transgender people  Children  Orphaned children
  • 38. 38

Editor's Notes

  • #24: EMPHASIZE that WHO clinical staging of HIV disease should only be used once HIV infection has been confirmed (serological and/or virological evidence of HIV infection). REFER participants to Handout 2.2.4 WHO Clinical Staging in Adults, Adolescents and Children on page 173 in the Participant Handbook.
  • #25: EMPHASIZE that WHO staging is done where HIV infection is confirmed by HIV antibody or virological testing. WHO HIV staging can be used in the absence of other immunological markers, as staging relies on the presentation of clinical features. Clinical staging can be used effectively without access to CD4 or other laboratory testing. However, CD4 testing is useful for determining the degree of immunocompromise, and where CD4 facilities are available they should be used to support and reinforce clinical decision-making. EMPHASIZE that CD4 levels are not necessary for starting ART but if available they are useful for knowing the degree of damage to the immune system and knowing the point at which treatment was initiated.
  • #27: REFER participants to Handout 4.2.1: WHO Clinical Staging of HIV/AIDS for Adults and Adolescents with Confirmed HIV Infection on Page 131. EXPLAIN this chart to participants, noting where various OIs fall in different stages. For each WHO category, let participants mention all possible OIs.