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MODULE 12:HIV AND
AIDS
CODE:HVA 1103
HOURS:30
CREDITS:3
Lecturer :Lydiah Cheyech
MODULE OUTCOMES
• This module is designed to enable the learner develop
self awareness in prevention and risk assessment of
HIV/AIDS to effectively contribute to the national HIV
response.
Module Units
• Fundamentals of HIV and AIDS
• Prevention of HIV infection and post exposure prophylaxis
• Behavior change communication and attitude training
• Opportunistic infections
• HIV treatment and monitoring
• Nutrition in the context of HIV & AIDS
• HIV testing and counseling (HTC)
OBJECTIVES
By the end of the module, the learner should;
Apply the knowledge of epidemiology of HIV in preventing
infection
Identify risks associated with exposure to HIV & AIDS
Demonstrate a positive attitude towards HIV & AIDS
management
Provide health education to PLWHA on prevention of
opportunistic infections
Monitor patients for ARV drug interactions
Provide nutritional education to clients/ patients suffering
from HIV & AIDS
Provide HIV& AIDS counseling to clients and patients
FUNDAMENTALS OF HIV &AIDS
Objectives
By the end of the lesson, the learner should be able to;
 Define common terms
 Explain the historical background of HIV/AIDS
 describe the global, regional, national and local epidemiology
and distribution of HIV
 State the modes of transmission and the key risk factors
 Explain the impact of HIV/AIDS on
individual,community,nationally and globally
 Describe the HIV/AIDS infection and disease progression
 State the WHO classification system of HIV/AIDS
Acronyms and Abbreviations
ADR Adverse drug reaction
AIDS Acquired immunodeficiency syndrome
ANC Antenatal care A&E
ART Antiretroviral therapy ARV Antiretroviral drug(s)
BF Breastfeeding
BMI Body Mass Index
BP Blood Pressure
CCC Comprehensive Care Centre
CHV Community Health Volunteer
Acronyms and Abbreviations
DNA Deoxyribonucleic acid
DRT Drug Resistance Testing
ECP Emergency contraceptive pill
EID Early Infant Diagnosis
eMTCT Elimination of Mother to Child Transmission
EPTB Extra-pulmonary Tuberculosis
FBC Full Blood Count
FBS Fasting Blood Sugar
FP Family Planning
GIT Gastro-intestinal tract
GOK Government of Kenya
GBV Gender-Based Violence
Acronyms and Abbreviations
Hb Hemoglobin
HCW Health Care Worker
HEI HIV Exposed Infant
HIV Human immunodeficiency virus
HIVST HIV self-testing
HTS HIV Testing Services
INH Isoniazid INSTI
IPT Isoniazid Preventive Therapy
KS Kaposi’s sarcoma
MOH Ministry of Health
MSM Men who have sex with men
MUAC Mid-upper arm circumference
NASCOP National AIDS and STI Control Program
Acronyms and Abbreviations
OI Opportunistic infection
PCP Pneumocystis jirovecii pneumonia
PCR Polymerase chain reaction
PEP Post-exposure prophylaxis
PITC Provider initiated HIV testing and counselling
PLHIV People living with HIV
PMTCT Prevention of mother-to-child transmission
PrEP Pre-exposure prophylaxis
PTB Pulmonary tuberculosis
PWID People who inject drugs
STI Sexually transmitted infection
TB Tuberculosis
VL Viral Load
DEFINATION
• HIV stands for Human Immunodeficiency Virus, the virus
that causes AIDS.
H: Human
I: Immunodeficiency
V: Virus
AIDS
AIDS stands for acquired immunodeficiency syndrome
and refers to the most advanced stage of HIV infection.
 A: Acquired — (not inherited) to differentiate from a
genetic or inherited condition
 I: Immuno — refers to the immune system
 D: Deficiency — inability to protect against illness
 S: Syndrome — a group of symptoms or illnesses that
occur as a result of the HIV infection
HIV & AIDS :HISTORICAL BAGROUND
• 1981
• Doctors in US recognized Pneumocytstis carinii
Pneumonia(PCP in homosexual males, a condition previously
unreported in healthy adults
• Later recognized that all these patients were
immunosuppressed
• 1983/4
• Scientist described the cause of this acquired
immunodeficiency syndrome (AIDS) as a retrovirus
• Lymphadenopathy Associated Virus (LAV)
• AIDs Associated Retrovirus (ARV)
• Human T- lymphotrophic Virus (HTLV)
Cont
• 1984
• First case described In Kenya
• 1986
• Human Immunodeficiency Virus (HIV) accepted as
international designation for the retrovirus in a WHO
consultative meeting
CONT……
• 1996……ARVs available in the world
• 1997……ARVs available in Kenya private sector
• 2003…..ARVs available in Kenya public sector
• 2005…..54,000 patients on ART
• 2010……Approx.426,870 patients on ART
EPIDEMIOLOGY OF HIV
HIV infection/AIDS is a global pandemic, especially in
developing countries. The current estimate of the number of
cases of HIV infection worldwide is ~33.2 million, two-thirds
of whom are in sub-Saharan Africa; ~50% of cases are in
women. HIV has continued to be a public health threat
globally.
In Kenya, over 1.5 million people are estimated to be living
with HIV, of whom 1,136,000 were on antiretroviral therapy by
December 2017.
CONT
• N/B
A pandemic is a global disease outbreak. HIV/AIDS is an
example of one of the most destructive global pandemics in
history.
ETIOLOGY
• HIV/AIDS is caused by infection by the human retroviruses
HIV-1 or -2.
• HIV-1 is the most common cause worldwide; HIV-2 has about
40% sequence homology
HIV VIRUS
virus is a small infectious agent that replicates only inside
the living cells of other organisms.
HIV belongs to a group known as retroviruses which carry
their genetic material in the form of ribonucleic acid(RNA).
A retrovirus from the Lentivirus family.
Viral particle is spherical in shape with a diameter of 80-
100 nanometers (nm).
HIV Structure
 Has an outer double lipid membrane, (derived from the
host membrane).
 The lipid membrane is lined by a matrix protein.
 The lipid membrane is studded with the surface
glycoprotein (gp) 120 and the transmembrane gp 41
protein.
 These glycoprotein spikes surround the cone-shaped
protein core.
Structure Of Human
Immunodeficiency Virus
cont….
HIV Glycoproteins
• The gp120 and gp41 mediate the entry of virus into the
host cells.
The core (capsid) is made up of several proteins:-
 P24 the main protein
 Within the capsid are
 two identical single strands of RNA (the viral genetic material).
 viral enzymes
Cont…..
Viral Enzymes
• Most important: Reverse Transcriptase (RT), Protease
and Integrase.
• RT converts viral single-stranded RNA into a double
stranded deoxyribonucleic acid (DNA).
• DNA is incorporated into host nucleus as the proviral
DNA.
• Integrase facilitates integration of the DNA into the host’s
chromosomal DNA.
• Protease enzyme splits generated macro-proteins into
smaller viral proteins (core, envelope & regulatory
proteins and enzymes) which go into forming new viral
particles.
TYPES OF HIV
Basic Virology:
There are two types of HIV.
• HIV – 1
• Is found worldwide
• Is the main cause of the worldwide pandemic
• HIV – 2
• Is mainly found in West Africa, Mozambique and
Angola.
• Causes a similar illness to HIV – 1
• Less efficiently transmissible rarely causing vertical
transmission
• Less aggressive with slower disease progression
HIV subtypes
• HIV-1 has many subtypes: A-K
• A-E are the predominant subtypes
• A: W. Africa, E. Africa, Central Africa East Europe
& Middle East
• B: N. America, Europe, Middle East, E. Asia, Latin
America
• C: S. Africa, S. Asia, Ethiopia
• D: E. Africa
• E: S. E. Asia
Distribution
East and Central
Africa has mainly
subtype A and D.
Southern Africa
mainly subtype
C.
West Africa
mainly A
Different
subtypes can
combine to form
diverse
recombinants.
Modes of HIV transmission
• HIV can be transmitted in the body through these fluids
which contains free virions and infected CD4 T cells:
• Semen
• Vaginal fluids
• Blood
• Breast milk
• Amniotic fluids.
• NOTE:
• Inflammation and breaks in the skin or mucosa results in
the increased probability that the HIV exposure will lead to
infection.
CONT……
Sexual Transmission
• Unprotected sexual intercourse with infected person.
• Direct contact with body fluids of infected person. (blood,
semen, vaginal secretions)
• Note: Sexual transmission accounts for 87% of HIV
transmission worldwide.
Mother to Child transmission
• During pregnancy
• During labour and delivery(most mother to child transmission
occurs at this stage).
• During breast feeding.
Parenteral
 Blood transfusion of infected blood or blood
products
 Exposure to infected blood or body fluids- IDU
through needle-sharing or needle stick
accidents
 Donated organs
% infection by transmission route
route transmission %
Sexual intercourse 70-80
Mother-to-child-transmission 5-10
Blood transfusion 3-5
Injecting drug use 5-10
Health care – eg needle stick injury <0.01
Risk factors
Unprotected sex – vaginal and anal sex.
Multiple sex partners.
STI infected people especially STIs that cause ulcerations like
herpes, chancroid and syphillis.
Use of intravenous drugs, Sharing needles.
Children born to HIV positive mothers.
Uncircumcised male.
Alcohol and drug addiction.
Occupational exposure; where precautions are neglected or fail
eg. Not using gloves or accidental needle prick injuries.
Blood transfusions especially where blood is not adequately
screened.
NOT Transmitted through:
• Sharing food or a drinking cup.
• Hugging
• Kissing
• Shaking hands
• Coughing or sneezing
• Being near a PLWHA
• Sharing latrines
• Mosquitoes or insect bites even if they carry human blood. HIV
cannot live outside humans.
MostAt Risk Populations for HIV infection.
(MARPS
• Injection drug users
• Sex workers and their clients.
• Men who have sex with men
• Prisoners
• Female sex workers
These groups are more vulnerable to HIV infection due a variety of
factors such as:
- More frequent exposures to the virus.
- Involvement in risky behavior.
- Potentially weak family and social support systems,
- Marginalization.
- Lack of resources
- Inadequate access to health care services,
- Stigma and Criminalization.
ASSIGNMENT
• Impact of HIV/AIDS on,
i. Individual
ii. Community
iii. Nation
iv. Globally
Impact on Morbidity and mortality of other
infections
People with HIV/AIDS are susceptible to other
infections
 Due to lowered immunity
High HIV prevalence increases the pool of people
with suppressed immunity
Any other infectious condition within such
population (e.g.TB) therefore finds a highly
susceptible group of people.
Impact on food security
 Food consumption decrease after the death of an adult in
the poorest households
 Reduction in agricultural work or even abandonment of
farms is likely.
 With fewer people, households farm smaller plots of land
or resort to less labor-intensive subsistence crops, which
often have lower nutritional or market value.
Impact on the health sector
 Stretched health budgets and systems.
 demand for out-patient services/ hospitalization
 Increased patient load and the staff shortages/staff
burnout.
 More time and money spent on diagnosing and
investigating cases.
 Demand for specialized services such as counselling also
increases
Impact on the education sector
 Decline in school enrolment
 Removal of children from school to care for parents and
family members
 Inability to afford school fees and other expenses
 AIDS-related infertility and a decline in birth rate
 Infection of more children who do not survive through the
years of schooling
HIV infection and disease progression
Immune System
HIV is an infectious disease therefore, its important to
understand how it integrates itself into persons immune system
and how the immune response plays a role .
The immune system functions as the body’s defense
mechanism against invasion.
Immunity: refers to the body’s specific protective response to
an invading foreign agent or organism.
Immune function is affected by age and by a variety of other
factors, such as central nervous system function, emotional
status, medications, the stress of illness, trauma, and surgery.
Cont
Normal immune system Consists of two arms;
• Innate (ancient) immune system
• Adaptive (acquired) immune system
• Innate immunity –
• It is non-specific and includes natural killer cell
lymphocytes that kill the target cells directly or indirectly
by antibody-dependent cellular cytotoxicity (ADCC), and
dendritic cells that localize and present antigens to
responsive T and B cells.
• Other participating cells are, monocytes, macrophages,
neutrophils, basophils, eosinophils, tissue mast cells and
epithelial cells.
Cont
• Adaptive immune system – Is characterized by antigen-
specific responses to a foreign antigen.
• It consists of cellular and humoral immunity.
• T cells are the main mediators of cellular immunity.
• The CD8 cytotoxic T cells target the virus-infected cells or
foreign cells while the CD4 T cells are the primary
regulatory cells of both cellular and humoral specific
immunity.
Cont
• The CD4 T cells activity can be either by direct cell
contact or indirectly by release of regulatory chemical
messengers called cytokines.
• The latter then activates the CD8 T cells, antibody-
producing B cells or monocytes and macrophages.
• The B cells are the principal effectors of humoral immunity
and leads to specific antibody production once activated.
Together, the innate and the adaptive immunity protect the
host from infections by multiple organisms.
IMMUNOLOGY
HIV attaches to cells of the immune systems with
specials surface markers called CD4 receptors
The following immune cells have CD4 receptors
 T-Lymphocytes – CD4 Cells
 Macrophages
 Monocytes
 Dendritic cells
Cont
• Many are genetically based, others are acquired.
Disorders of the immune system may stem from excesses
or deciencies of immunocompetent cells, alterations in
the function of these cells, immunologic attack on self-
antigens, or inappropriate or exaggerated responses to
specic.
Cont
When an infectious agents enters the body by tackling the
skin and the mucous membrane barries, then its tackled
by cellular elements and tissue macrophages which
activates specific immune response (antibodies,sensitised
T cells, memory cells )
Cont
• When the virus enters the body and gets into the blood
stream, it binds itself to specific defence cells known as
CD4 lymphocytes. When the retrovirus enters the CD4
cell, an enzyme from the virus called reverse
transcriptase takes over the cells genetic equipment to
produce more retroviruses which are released outside
the infected cell and go on to infect and destroy other
CD4 cells.
• This process goes on over a period of years during which
the number of CD4 lymphocytes gradually decreases.
Cont
• NOTE:
• although the body of an infected person struggles to
form antibodies against the HIV, these antibodies
cannot destroy all the viruses because they keep on
multiplying and the body's defense system is being
depleted and is, therefore, unable to produce enough
antibodies to match the viruses.
CD4 CELLS
CD4 cells are the immune cells that protect the body from
infections
They prevent infections and keeps the body healthy
CD4 cells are measured through a blood test, called CD4
count. For adults a normal CD4 count is above 500
How are CD4 cells affected by HIV –
 HIV attacks and destroys CD4 cells - After years of
constant attack from HIV, the CD4 count falls (usually
below 200), diseases called “opportunistic infections” are
able to infect the body because the body cannot defend
itself.
Cont
• Common opportunistic infections include: tuberculosis,
pneumonia, skin problems, and chronic diarrhea
• Once treatment for HIV started, VL test to monitor
response to anti-retroviral treatment done.
HIV life cycle
• All virus target specific cells.
• HIV targets cells with CD4+ receptors which are
expressed on the surface of T lymphocytes ,monocytes,
dendrites cells and brain microglia.
• During acute/recent infection, the virus use chemokine
receptors for entry to T cells.
Attachment
Gp 120 and Gp 41(glycoproteins of HIV) bind with the
hosts uninfected CD4+ receptors and chemokine
coreceptors which results in fusion.
Life cycle Cont.…..
UNCOATING
• The content of viral core(2 single strands of viral RNA and
3 viral enzymes, reverse transcriptase,integrase and
protease) are emptied into the CD4+ T cell.
DNA Synthesis
HIV changes its genetic material from RNA to DNA through
action of reverse transcriptase resulting to double stranded
DNA that carries instruction for viral replication.
Life Cycle cont…..
Intergration
• New viral DNA enters the nucleus of the CD4+ T cells and
through the action of intergrase is blended with the DNA
of the CD4+ T cell, resulting in permanent lifelong
infection.
• NOTE:
• Prior to this, the uninfected person has only been
exposed to and not infected.
Cont…
Transcription
• When the CD4+ T cells is activated, the double stranded
DNA forms a single stranded messenger RNA(mRNA)
which binds new viruses
Translation
• The mRNA creates chains of new proteins and
enzymes(polyproteins) that contain the components
needed in the construction of new viruses.
Cleavage
• The HIV enzyme protease cuts the polyprotein chain into
the individual proteins that make up the new virus
Cont…….
Budding
• New protein and viral RNA migrate to the membrane of
the infected CD4+ T cell exit from the cell and start the
process all over.
• The CD4 cells are often destroyed by HIV virus infection
and replication resulting in profound immunodeficiency.
Cont….
Host immune response during HIV
infection(phases)
Primary HIV Infection
The period from infection with HIV to the development of
antibodies . During this period, there is intense viral
replication and widespread dissemination of HIV
throughout the body. Symptoms associated with the
viremia range from none to severe flu-like symptoms.
During the primary infection period, the window period
occurs because a person is infected with HIV but tests
negative on the HIV antibody blood test.
Asymptomatic Phase
 Can last from 2 to 15 years – range mainly due to genetic
differences in patient
 Virus replicates in lymphoid tissue, CD4 cells at high rates
 CD4 levels gradually decline
 Immunity gradually weakens
 Patients remain asymptomatic
 Patients are infectious
Symptomatic Phase (progression to
AIDS)
 Approximately 10 to 12 years after infection
 Increased demands on immune system
 Production of CD4 cells cannot match destruction,
immune system fails
 Viral load reaches extremely high levels
 Increased risk of opportunistic infections and tumours
 Progression to AIDS
Classification system of HIV
For Adults and Adolescents
Stage 1
Asymptomatic
 Persistent Generalized Lymphadenopathy (PGL)

Stage 2
 Moderate unexplained weight loss (< 10% of presumed
or measured body weight)
 Minor mucocutaneous manifestations (seborrheic
dermatitis, papular pruritic eruptions, fungal nail
infections, recurrent oral ulcerations, angular cheilitis) •
Herpes zoster
 Recurrent upper respiratory tract infections (sinusitis,
tonsillitis, bronchitis, otitis media, pharyngitis)
Stage 3
Unexplained severe weight loss (over 10% of presumed
or measured body weight)
Unexplained chronic diarrhoea for longer than one month
Unexplained persistent fever (intermittent or constant for
longer than one month)
Persistent oral candidiasis
Oral hairy leukoplakia
Pulmonary tuberculosis
Cont
Severe bacterial infections (e.g. pneumonia, empyema,
pyomyositis, bone or joint infection, meningitis,
bacteraemia)
Acute necrotizing ulcerative stomatitis, gingivitis or
periodontitis
 Unexplained anaemia (below 8 g/dl ), neutropenia (below
0.5 x 109/l) and/or chronic thrombocytopenia (below 50 x
109 /l)
Stage 4
 HIV wasting syndrome
Pneumocystis jirovecipneumonia (PCP)
 Recurrent severe bacterial pneumonia (≥ 2 episodes
within 1 year) Cryptococcal meningitis
 Toxoplasmosis of the brain
CONT
genital or ano-rectal herpes simplex infection for > 1
month
Kaposi’s sarcoma (KS)
HIV encephalopathy
 Extra pulmonary tuberculosis (EPTB) Conditions where
confirmatory diagnostic testing is necessary
 Cryptosporidiosis, with diarrhoea > 1 month
 Isosporiasis
Cont
Cryptococcosis (extra pulmonary)
 Disseminated non-tuberculous mycobacterial infection
 Cytomegalovirus (CMV) retinitis or infection of the organs
(other than liver, spleen, or lymph nodes)
Progressive multifocal leucoencephalopathy (PML)
 Any disseminated mycosis (e.g. histoplasmosis,
coccidiomycosis)
 Candidiasis of the oesophagus or airways
 Non-typhoid salmonella (NTS)
septicaemia
Cont
• Lymphoma cerebral or B cell Non-Hodgkin’s Lymphoma
• Invasive cervical cancer
• Visceral leishmaniasis
• Symptomatic HIV-associated nephropathy or HIV
associated cardiomyopathy

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HIV & AIDS L1.pptx

  • 1. MODULE 12:HIV AND AIDS CODE:HVA 1103 HOURS:30 CREDITS:3 Lecturer :Lydiah Cheyech
  • 2. MODULE OUTCOMES • This module is designed to enable the learner develop self awareness in prevention and risk assessment of HIV/AIDS to effectively contribute to the national HIV response.
  • 3. Module Units • Fundamentals of HIV and AIDS • Prevention of HIV infection and post exposure prophylaxis • Behavior change communication and attitude training • Opportunistic infections • HIV treatment and monitoring • Nutrition in the context of HIV & AIDS • HIV testing and counseling (HTC)
  • 4. OBJECTIVES By the end of the module, the learner should; Apply the knowledge of epidemiology of HIV in preventing infection Identify risks associated with exposure to HIV & AIDS Demonstrate a positive attitude towards HIV & AIDS management Provide health education to PLWHA on prevention of opportunistic infections Monitor patients for ARV drug interactions Provide nutritional education to clients/ patients suffering from HIV & AIDS Provide HIV& AIDS counseling to clients and patients
  • 5. FUNDAMENTALS OF HIV &AIDS Objectives By the end of the lesson, the learner should be able to;  Define common terms  Explain the historical background of HIV/AIDS  describe the global, regional, national and local epidemiology and distribution of HIV  State the modes of transmission and the key risk factors  Explain the impact of HIV/AIDS on individual,community,nationally and globally  Describe the HIV/AIDS infection and disease progression  State the WHO classification system of HIV/AIDS
  • 6. Acronyms and Abbreviations ADR Adverse drug reaction AIDS Acquired immunodeficiency syndrome ANC Antenatal care A&E ART Antiretroviral therapy ARV Antiretroviral drug(s) BF Breastfeeding BMI Body Mass Index BP Blood Pressure CCC Comprehensive Care Centre CHV Community Health Volunteer
  • 7. Acronyms and Abbreviations DNA Deoxyribonucleic acid DRT Drug Resistance Testing ECP Emergency contraceptive pill EID Early Infant Diagnosis eMTCT Elimination of Mother to Child Transmission EPTB Extra-pulmonary Tuberculosis FBC Full Blood Count FBS Fasting Blood Sugar FP Family Planning GIT Gastro-intestinal tract GOK Government of Kenya GBV Gender-Based Violence
  • 8. Acronyms and Abbreviations Hb Hemoglobin HCW Health Care Worker HEI HIV Exposed Infant HIV Human immunodeficiency virus HIVST HIV self-testing HTS HIV Testing Services INH Isoniazid INSTI IPT Isoniazid Preventive Therapy KS Kaposi’s sarcoma MOH Ministry of Health MSM Men who have sex with men MUAC Mid-upper arm circumference NASCOP National AIDS and STI Control Program
  • 9. Acronyms and Abbreviations OI Opportunistic infection PCP Pneumocystis jirovecii pneumonia PCR Polymerase chain reaction PEP Post-exposure prophylaxis PITC Provider initiated HIV testing and counselling PLHIV People living with HIV PMTCT Prevention of mother-to-child transmission PrEP Pre-exposure prophylaxis PTB Pulmonary tuberculosis PWID People who inject drugs STI Sexually transmitted infection TB Tuberculosis VL Viral Load
  • 10. DEFINATION • HIV stands for Human Immunodeficiency Virus, the virus that causes AIDS. H: Human I: Immunodeficiency V: Virus
  • 11. AIDS AIDS stands for acquired immunodeficiency syndrome and refers to the most advanced stage of HIV infection.  A: Acquired — (not inherited) to differentiate from a genetic or inherited condition  I: Immuno — refers to the immune system  D: Deficiency — inability to protect against illness  S: Syndrome — a group of symptoms or illnesses that occur as a result of the HIV infection
  • 12. HIV & AIDS :HISTORICAL BAGROUND • 1981 • Doctors in US recognized Pneumocytstis carinii Pneumonia(PCP in homosexual males, a condition previously unreported in healthy adults • Later recognized that all these patients were immunosuppressed • 1983/4 • Scientist described the cause of this acquired immunodeficiency syndrome (AIDS) as a retrovirus • Lymphadenopathy Associated Virus (LAV) • AIDs Associated Retrovirus (ARV) • Human T- lymphotrophic Virus (HTLV)
  • 13. Cont • 1984 • First case described In Kenya • 1986 • Human Immunodeficiency Virus (HIV) accepted as international designation for the retrovirus in a WHO consultative meeting
  • 14. CONT…… • 1996……ARVs available in the world • 1997……ARVs available in Kenya private sector • 2003…..ARVs available in Kenya public sector • 2005…..54,000 patients on ART • 2010……Approx.426,870 patients on ART
  • 15. EPIDEMIOLOGY OF HIV HIV infection/AIDS is a global pandemic, especially in developing countries. The current estimate of the number of cases of HIV infection worldwide is ~33.2 million, two-thirds of whom are in sub-Saharan Africa; ~50% of cases are in women. HIV has continued to be a public health threat globally. In Kenya, over 1.5 million people are estimated to be living with HIV, of whom 1,136,000 were on antiretroviral therapy by December 2017.
  • 16. CONT • N/B A pandemic is a global disease outbreak. HIV/AIDS is an example of one of the most destructive global pandemics in history.
  • 17. ETIOLOGY • HIV/AIDS is caused by infection by the human retroviruses HIV-1 or -2. • HIV-1 is the most common cause worldwide; HIV-2 has about 40% sequence homology
  • 18. HIV VIRUS virus is a small infectious agent that replicates only inside the living cells of other organisms. HIV belongs to a group known as retroviruses which carry their genetic material in the form of ribonucleic acid(RNA). A retrovirus from the Lentivirus family. Viral particle is spherical in shape with a diameter of 80- 100 nanometers (nm).
  • 19. HIV Structure  Has an outer double lipid membrane, (derived from the host membrane).  The lipid membrane is lined by a matrix protein.  The lipid membrane is studded with the surface glycoprotein (gp) 120 and the transmembrane gp 41 protein.  These glycoprotein spikes surround the cone-shaped protein core.
  • 21. cont…. HIV Glycoproteins • The gp120 and gp41 mediate the entry of virus into the host cells. The core (capsid) is made up of several proteins:-  P24 the main protein  Within the capsid are  two identical single strands of RNA (the viral genetic material).  viral enzymes
  • 22. Cont….. Viral Enzymes • Most important: Reverse Transcriptase (RT), Protease and Integrase. • RT converts viral single-stranded RNA into a double stranded deoxyribonucleic acid (DNA). • DNA is incorporated into host nucleus as the proviral DNA. • Integrase facilitates integration of the DNA into the host’s chromosomal DNA. • Protease enzyme splits generated macro-proteins into smaller viral proteins (core, envelope & regulatory proteins and enzymes) which go into forming new viral particles.
  • 23. TYPES OF HIV Basic Virology: There are two types of HIV. • HIV – 1 • Is found worldwide • Is the main cause of the worldwide pandemic • HIV – 2 • Is mainly found in West Africa, Mozambique and Angola. • Causes a similar illness to HIV – 1 • Less efficiently transmissible rarely causing vertical transmission • Less aggressive with slower disease progression
  • 24. HIV subtypes • HIV-1 has many subtypes: A-K • A-E are the predominant subtypes • A: W. Africa, E. Africa, Central Africa East Europe & Middle East • B: N. America, Europe, Middle East, E. Asia, Latin America • C: S. Africa, S. Asia, Ethiopia • D: E. Africa • E: S. E. Asia
  • 25. Distribution East and Central Africa has mainly subtype A and D. Southern Africa mainly subtype C. West Africa mainly A Different subtypes can combine to form diverse recombinants.
  • 26. Modes of HIV transmission • HIV can be transmitted in the body through these fluids which contains free virions and infected CD4 T cells: • Semen • Vaginal fluids • Blood • Breast milk • Amniotic fluids. • NOTE: • Inflammation and breaks in the skin or mucosa results in the increased probability that the HIV exposure will lead to infection.
  • 27. CONT…… Sexual Transmission • Unprotected sexual intercourse with infected person. • Direct contact with body fluids of infected person. (blood, semen, vaginal secretions) • Note: Sexual transmission accounts for 87% of HIV transmission worldwide. Mother to Child transmission • During pregnancy • During labour and delivery(most mother to child transmission occurs at this stage). • During breast feeding.
  • 28. Parenteral  Blood transfusion of infected blood or blood products  Exposure to infected blood or body fluids- IDU through needle-sharing or needle stick accidents  Donated organs
  • 29. % infection by transmission route route transmission % Sexual intercourse 70-80 Mother-to-child-transmission 5-10 Blood transfusion 3-5 Injecting drug use 5-10 Health care – eg needle stick injury <0.01
  • 30. Risk factors Unprotected sex – vaginal and anal sex. Multiple sex partners. STI infected people especially STIs that cause ulcerations like herpes, chancroid and syphillis. Use of intravenous drugs, Sharing needles. Children born to HIV positive mothers. Uncircumcised male. Alcohol and drug addiction. Occupational exposure; where precautions are neglected or fail eg. Not using gloves or accidental needle prick injuries. Blood transfusions especially where blood is not adequately screened.
  • 31. NOT Transmitted through: • Sharing food or a drinking cup. • Hugging • Kissing • Shaking hands • Coughing or sneezing • Being near a PLWHA • Sharing latrines • Mosquitoes or insect bites even if they carry human blood. HIV cannot live outside humans.
  • 32. MostAt Risk Populations for HIV infection. (MARPS • Injection drug users • Sex workers and their clients. • Men who have sex with men • Prisoners • Female sex workers These groups are more vulnerable to HIV infection due a variety of factors such as: - More frequent exposures to the virus. - Involvement in risky behavior. - Potentially weak family and social support systems, - Marginalization. - Lack of resources - Inadequate access to health care services, - Stigma and Criminalization.
  • 33. ASSIGNMENT • Impact of HIV/AIDS on, i. Individual ii. Community iii. Nation iv. Globally
  • 34. Impact on Morbidity and mortality of other infections People with HIV/AIDS are susceptible to other infections  Due to lowered immunity High HIV prevalence increases the pool of people with suppressed immunity Any other infectious condition within such population (e.g.TB) therefore finds a highly susceptible group of people.
  • 35. Impact on food security  Food consumption decrease after the death of an adult in the poorest households  Reduction in agricultural work or even abandonment of farms is likely.  With fewer people, households farm smaller plots of land or resort to less labor-intensive subsistence crops, which often have lower nutritional or market value.
  • 36. Impact on the health sector  Stretched health budgets and systems.  demand for out-patient services/ hospitalization  Increased patient load and the staff shortages/staff burnout.  More time and money spent on diagnosing and investigating cases.  Demand for specialized services such as counselling also increases
  • 37. Impact on the education sector  Decline in school enrolment  Removal of children from school to care for parents and family members  Inability to afford school fees and other expenses  AIDS-related infertility and a decline in birth rate  Infection of more children who do not survive through the years of schooling
  • 38. HIV infection and disease progression Immune System HIV is an infectious disease therefore, its important to understand how it integrates itself into persons immune system and how the immune response plays a role . The immune system functions as the body’s defense mechanism against invasion. Immunity: refers to the body’s specic protective response to an invading foreign agent or organism. Immune function is affected by age and by a variety of other factors, such as central nervous system function, emotional status, medications, the stress of illness, trauma, and surgery.
  • 39. Cont Normal immune system Consists of two arms; • Innate (ancient) immune system • Adaptive (acquired) immune system • Innate immunity – • It is non-specific and includes natural killer cell lymphocytes that kill the target cells directly or indirectly by antibody-dependent cellular cytotoxicity (ADCC), and dendritic cells that localize and present antigens to responsive T and B cells. • Other participating cells are, monocytes, macrophages, neutrophils, basophils, eosinophils, tissue mast cells and epithelial cells.
  • 40. Cont • Adaptive immune system – Is characterized by antigen- specific responses to a foreign antigen. • It consists of cellular and humoral immunity. • T cells are the main mediators of cellular immunity. • The CD8 cytotoxic T cells target the virus-infected cells or foreign cells while the CD4 T cells are the primary regulatory cells of both cellular and humoral specific immunity.
  • 41. Cont • The CD4 T cells activity can be either by direct cell contact or indirectly by release of regulatory chemical messengers called cytokines. • The latter then activates the CD8 T cells, antibody- producing B cells or monocytes and macrophages. • The B cells are the principal effectors of humoral immunity and leads to specific antibody production once activated. Together, the innate and the adaptive immunity protect the host from infections by multiple organisms.
  • 42. IMMUNOLOGY HIV attaches to cells of the immune systems with specials surface markers called CD4 receptors The following immune cells have CD4 receptors  T-Lymphocytes – CD4 Cells  Macrophages  Monocytes  Dendritic cells
  • 43. Cont • Many are genetically based, others are acquired. Disorders of the immune system may stem from excesses or deciencies of immunocompetent cells, alterations in the function of these cells, immunologic attack on self- antigens, or inappropriate or exaggerated responses to specic.
  • 44. Cont When an infectious agents enters the body by tackling the skin and the mucous membrane barries, then its tackled by cellular elements and tissue macrophages which activates specific immune response (antibodies,sensitised T cells, memory cells )
  • 45. Cont • When the virus enters the body and gets into the blood stream, it binds itself to specific defence cells known as CD4 lymphocytes. When the retrovirus enters the CD4 cell, an enzyme from the virus called reverse transcriptase takes over the cells genetic equipment to produce more retroviruses which are released outside the infected cell and go on to infect and destroy other CD4 cells. • This process goes on over a period of years during which the number of CD4 lymphocytes gradually decreases.
  • 46. Cont • NOTE: • although the body of an infected person struggles to form antibodies against the HIV, these antibodies cannot destroy all the viruses because they keep on multiplying and the body's defense system is being depleted and is, therefore, unable to produce enough antibodies to match the viruses.
  • 47. CD4 CELLS CD4 cells are the immune cells that protect the body from infections They prevent infections and keeps the body healthy CD4 cells are measured through a blood test, called CD4 count. For adults a normal CD4 count is above 500 How are CD4 cells affected by HIV –  HIV attacks and destroys CD4 cells - After years of constant attack from HIV, the CD4 count falls (usually below 200), diseases called “opportunistic infections” are able to infect the body because the body cannot defend itself.
  • 48. Cont • Common opportunistic infections include: tuberculosis, pneumonia, skin problems, and chronic diarrhea • Once treatment for HIV started, VL test to monitor response to anti-retroviral treatment done.
  • 49. HIV life cycle • All virus target specific cells. • HIV targets cells with CD4+ receptors which are expressed on the surface of T lymphocytes ,monocytes, dendrites cells and brain microglia. • During acute/recent infection, the virus use chemokine receptors for entry to T cells. Attachment Gp 120 and Gp 41(glycoproteins of HIV) bind with the hosts uninfected CD4+ receptors and chemokine coreceptors which results in fusion.
  • 50. Life cycle Cont.….. UNCOATING • The content of viral core(2 single strands of viral RNA and 3 viral enzymes, reverse transcriptase,integrase and protease) are emptied into the CD4+ T cell. DNA Synthesis HIV changes its genetic material from RNA to DNA through action of reverse transcriptase resulting to double stranded DNA that carries instruction for viral replication.
  • 51. Life Cycle cont….. Intergration • New viral DNA enters the nucleus of the CD4+ T cells and through the action of intergrase is blended with the DNA of the CD4+ T cell, resulting in permanent lifelong infection. • NOTE: • Prior to this, the uninfected person has only been exposed to and not infected.
  • 52. Cont… Transcription • When the CD4+ T cells is activated, the double stranded DNA forms a single stranded messenger RNA(mRNA) which binds new viruses Translation • The mRNA creates chains of new proteins and enzymes(polyproteins) that contain the components needed in the construction of new viruses. Cleavage • The HIV enzyme protease cuts the polyprotein chain into the individual proteins that make up the new virus
  • 53. Cont……. Budding • New protein and viral RNA migrate to the membrane of the infected CD4+ T cell exit from the cell and start the process all over. • The CD4 cells are often destroyed by HIV virus infection and replication resulting in profound immunodeficiency.
  • 55. Host immune response during HIV infection(phases) Primary HIV Infection The period from infection with HIV to the development of antibodies . During this period, there is intense viral replication and widespread dissemination of HIV throughout the body. Symptoms associated with the viremia range from none to severe flu-like symptoms. During the primary infection period, the window period occurs because a person is infected with HIV but tests negative on the HIV antibody blood test.
  • 56. Asymptomatic Phase  Can last from 2 to 15 years – range mainly due to genetic differences in patient  Virus replicates in lymphoid tissue, CD4 cells at high rates  CD4 levels gradually decline  Immunity gradually weakens  Patients remain asymptomatic  Patients are infectious
  • 57. Symptomatic Phase (progression to AIDS)  Approximately 10 to 12 years after infection  Increased demands on immune system  Production of CD4 cells cannot match destruction, immune system fails  Viral load reaches extremely high levels  Increased risk of opportunistic infections and tumours  Progression to AIDS
  • 58. Classification system of HIV For Adults and Adolescents Stage 1 Asymptomatic  Persistent Generalized Lymphadenopathy (PGL) 
  • 59. Stage 2  Moderate unexplained weight loss (< 10% of presumed or measured body weight)  Minor mucocutaneous manifestations (seborrheic dermatitis, papular pruritic eruptions, fungal nail infections, recurrent oral ulcerations, angular cheilitis) • Herpes zoster  Recurrent upper respiratory tract infections (sinusitis, tonsillitis, bronchitis, otitis media, pharyngitis)
  • 60. Stage 3 Unexplained severe weight loss (over 10% of presumed or measured body weight) Unexplained chronic diarrhoea for longer than one month Unexplained persistent fever (intermittent or constant for longer than one month) Persistent oral candidiasis Oral hairy leukoplakia Pulmonary tuberculosis
  • 61. Cont Severe bacterial infections (e.g. pneumonia, empyema, pyomyositis, bone or joint infection, meningitis, bacteraemia) Acute necrotizing ulcerative stomatitis, gingivitis or periodontitis  Unexplained anaemia (below 8 g/dl ), neutropenia (below 0.5 x 109/l) and/or chronic thrombocytopenia (below 50 x 109 /l)
  • 62. Stage 4  HIV wasting syndrome Pneumocystis jirovecipneumonia (PCP)  Recurrent severe bacterial pneumonia (≥ 2 episodes within 1 year) Cryptococcal meningitis  Toxoplasmosis of the brain
  • 63. CONT genital or ano-rectal herpes simplex infection for > 1 month Kaposi’s sarcoma (KS) HIV encephalopathy  Extra pulmonary tuberculosis (EPTB) Conditions where confirmatory diagnostic testing is necessary  Cryptosporidiosis, with diarrhoea > 1 month  Isosporiasis
  • 64. Cont Cryptococcosis (extra pulmonary)  Disseminated non-tuberculous mycobacterial infection  Cytomegalovirus (CMV) retinitis or infection of the organs (other than liver, spleen, or lymph nodes) Progressive multifocal leucoencephalopathy (PML)  Any disseminated mycosis (e.g. histoplasmosis, coccidiomycosis)  Candidiasis of the oesophagus or airways  Non-typhoid salmonella (NTS) septicaemia
  • 65. Cont • Lymphoma cerebral or B cell Non-Hodgkin’s Lymphoma • Invasive cervical cancer • Visceral leishmaniasis • Symptomatic HIV-associated nephropathy or HIV associated cardiomyopathy