Hiv Aids

HIV/AIDS
Aetiology
The Human Immunodeficiency Virus (HIV) is a retrovirus of the lenti-virus family that affects the
human T cells.
HIV is cytolytic for T cells causing immunodeficiency.
HIV exists in 2 forms - HIV–1 (commonest cause and is responsible for the global pandemic) and HIV–
2 (largely confined to certain parts of West – Africa)
Transmission
 Sexual transmission
Predominant mode of infection (70 – 80%)
Virus is carried in the body fluids (semen, vaginal secretions and fluids, cervical cells).
 Parenteral transmission
Occurs in three main groups such as IV drug abusers, Haemophiliacs and random recipients of
blood and blood products
 Mother-to-child transmission
Infected mothers can transmit the infection to their offspring by three routes in utero by
placental spread, during childbirth/delivery through an infected birth canal and after birth by
breastfeeding
 Organ and tissue donation
Factors influencing transmission
Factors Increasing HIV Transmission
 High Viral load in the infecting person

 Lowered Immune status of the recipient
 Presence of genital ulcers, abrasions
 Lack of circumcision (male)
 Multiple sexual partners
 Specific sexual practice – anal sex
 Type of the HIV strain infecting recipient
Factors decreasing HIV Transmission
 Avoiding exposure (abstinence)

 Use of condoms during all sexual encounters
 Treatment of concurrent sexually Transmitted Infections (STIs)
 Post-exposure prophylaxis
 Antiretroviral therapy to prevent mother to child transmission
The HIV life cycle
1. Binding (Attachment)
• HIV attaches to the surface of target cells CD4 at specific sites - CD4 receptor and chemokine co-
receptor must attach successfully to both sites in order to fuse with CD 4 cellular membranes)
• The gp 120 undergoes conformational changes enabling interaction between gp 120 and co-
receptors, the chemokines so as to facilitate entry of the virus.
2. Fusion, Viral Entry and Uncoating
• The interaction between the virus and its receptors triggers conformational changes in gp 41.
• After fusion the virus core containing the HIV genome enters cytoplasm of the cell
• Once inside the virus uncoats and injects its protein coat/core into the cell as well as its two single
strands of viral RNA. The viral RNA carries instructions for producing more viruses.
3. Reverse Transcription
• Once the HIV genome is internalized, the viral single strand RNA converts to double stranded viral
DNA. HIV uses an enzyme called reverse-transcriptase
• The enzyme travels along the viral RNA strand and makes a copy
• The new strand is then copied again but in reverse (in a mirror like image). The result of this
process is double – stranded viral DNA
4. Integration
• New viral DNA (cDNA) enters the nucleus of the CD4 cell.
•Through the action of enzyme integrase, the cell is able to fuse with the nucleus. Integrase then
inserts the viral DNA into the cellular DNA to form a provirus
• After integration the provirus may remain locked into the chromosome for months or years (latent
infection).
5. Proviral Transcription
• Viral DNA programs the CD4 cellular machinery to produce components necessary for the
formation of new viruses.
• Viral RNA which will serve as the genetic material for newly produced viral messenger RNA (mRNA)
which will produce a chain of proteins also called Poly-proteins.
6. Translation
• A chain of polyproteins is created using instructions encoded by mRNA
• These proteins are essential for the construction of new viruses
• The new viruses that are formed are used in the next stages
7. Cleavage and Budding
• Protease enzyme is one of the proteins formed in the polyprotein chain. It cuts or cleaves the
polyprotein chain into individual proteins.
• These proteins are necessary to complete the assembly of new infectious HIV.
• The newly formed viral particle buds off from the cell membrane of the infected cells taking with it
the cellular bi-lipid layer.
 Extensive viral budding causes cell death (target cell) and formation numerous new viruses.
8. Assemble, Maturation and Release
• New viral proteins and new viral RNA are gathered together at cell membrane and assembled into
new viruses.
 Once they complete maturation process and become fully functional and infectious viruses, they
are released to infect new CD4 cells.
Signs and Symptoms (Clinical features)
Staging of HIV/AIDS
WHO Stage 1
 Asymptomatic HIV infection

 Persistent Generalized Lymphadenopathy(PGL)
WHO Stage 2
 Moderate weight loss

 Herpes Zoster
 Minor mucocutaneous manifestations (dermatitis, fungal infection)
 Recurrent upper respiratory tract Infections
WHO Stage 3
• Severe weight loss
 Unexplained chronic diarrhoea (> 1 month)

 Unexplained prolonged fever (intermittent or constant > 1 month)
 Oral Candidiasis (thrush)
 Tuberculosis, pulmonary
 Severe bacterial infections (pneumonia)
WHO Stage 4
 HIV wasting syndrome

 Recurrent severe bacterial pneumonia
 Cryptococcal meningitis
 Toxoplasmosis of the brain
 Kaposi sarcoma (KS)
 Extra pulmonary tuberculosis(EPTB)

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HIV/AIDS

HIV is cytolytic for T cells causing immunodeficiency.

Factors influencing transmission

Factors Increasing HIV Transmission

 High Viral load in the infecting person

Factors decreasing HIV Transmission

 Avoiding exposure (abstinence)

2. Fusion, Viral Entry and Uncoating

• A chain of polyproteins is created using instructions encoded by mRNA

• These proteins are essential for the construction of new viruses

7. Cleavage and Budding

8. Assemble, Maturation and Release

Signs and Symptoms (Clinical features)

 Asymptomatic HIV infection

 Moderate weight loss

• Severe weight loss

 Unexplained chronic diarrhoea (> 1 month)

 HIV wasting syndrome

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