HIV & AIDS

2. INTRODUCTION

First indication came in 1981 from New York and LA,of a sudden outbreak
of two very rare diseases, Kaposi sarcoma and Pneumocystis carini
pneumonia in young adults who were homosexuals or addicted to injected
narcotics. This condition was named AIDS.

Discovered independently by Luc Montagnier of France and Robert Gallo
of the US in 1983-84

AIDS in India was 1st detected in commercial sex workers in
Tamil Nadu in 1986& has been growing very fast since then.

Causative agent- Human Immunodeficiency Virus(HIV), lentivirus
subgroup of family retroviridae.

AIDS is a global pandemic

2007-33.2 million individuals living with AIDS

4. ROUTES OF TRANSMISSION

Sexual route

IV drug use

Mother to baby

Body fluids

5. HUMAN IMMUNODEFICIENCY VIRUS



Icosehadral(20 sided)
enveloped virus
90-120 nm in size
Outer icosehedral shell and a
inner core enclosing RNAs

6. 
2 genetically different but related forms of HIV-HIV1
and HIV 2

HIV 2 more common in India

On basis of genetic analysis,HIV 1 can be subdivided
into 3 subgroups-M(major).O(outlier),N(neither)

Group M most common worldwide

M further divided into subtypes A to K.

Clade C is the fastest spreading worldwide.

7. THE HIV GENOME
Structural genes-gag, pol, env
 Nonstructural genes and regulatory genes tat (transactivating gene)
 nef (negative effector gene)
 rev (regulator of virus gene)
 vif (viral infectivity factor gene)
 vpu (viral protein U)
 vpr (viral protein R)
 LTR (long terminal repeat)


9. PATHOGENESIS
Two major targets of HIV-immune system and central
nervous system
 Profound cell mediated immunodeficiency is the
hallmark
 Mainly affects CD4+Tcells,dendritic cells and
macrophages.
 Enters body through mucosal tissues and blood--infects T cells,dendritic cells and macrophages--infection establishes in lymphoid organs---virus
remains latent ----active viral replication associated
with infection


11. In addition to direct killing of CD4+T cells,other mechanisms are:
 HIV cause progressive architectural and cellular destruction of
lymph nodes
 Chronic activation of uninfected cells leads to activation induced
cell death
 Loss of precursors of CD4+ T cells
 Fusion of infected and uninfected cells-leads to balloning and cell
death
 Apoptosis of uninfected CD4+T cells by binding of soluble gp120 to
CD4 molecule—activation through T cell receptorby antigens

13. INFECTION OF NON T CELLS

Macrophages

HIV1 can infect and multiply in terminally differentiated macrophages
They are reservoirs of infection

Dendritic cells


Mucosal dendritic cells transport to regional lymph nodes
Follicular ones are potent reservoir

B cells


Polyclonal activation ---germinal centre B cell hyperplasia, BM
plasmacytosis, hypergammaglobulinimia, formation of circulating immune
complexes

14. MAJOR ABNORMALITIES OF IMMUNE SYSTEM

Decreased T cell function:

Preferential loss of activated and memory T cells
Decreased delayed type hypersensitivity
Susceptibility to opportunistic infection
Susceptibility to neoplasm

Polyclonal B cell activation :




Hypergammaglobulinimia,circulating immune complexes
Inability to mount immune response to new antigens

Altered monocyte/macrophage function:




Decreased chemotaxis and phagocytosis
Decrease class II MHC expression
Diminished capacity to present antigen to T cells

15. NATURAL HISTORY OF HIV INFECTION

18. T CE

19. CDC CLASSIFICATION CATEGORIES OF HIV
Clinical categories
1
≥500cells/μl
2
200-499cells/μl
3
≤200cells/μl
A.asymptomatic,acute
HIV,persistent
generalized
lymphadenopathy
A1
A2
A3
B.Symptomatic ,not A
or C
B1
B2
B3
C.AIDS indicator
conditions

20. AIDS DEFINING OPPORTUNISTIC INFECTION AND NEOPLASMS

Protozoal and helminthic infection

Cryptosporidiosis
Toxoplasmosis

Fungal infection


Pneumocystosis
Candidiasis
Cryptococcosis
Coccidioidomycosis
Histoplasmosis

Bacterial infections





Mycobacteriosis
Nocardiosis

Viral infections





Cytomegalovirus
HSV
Varicella zoster
Progressive multifocal leukoencephalopathy

21. NEOPLASMS

Kaposi’s sarcoma

Non-hodgkin B cell lymphoma

Cervical cancer in women

Anal cancer in men
25-40% of HIV patients develop malignancy

22. ORAL CANDIDIASIS

23. KAPOSI SARCOMA

24. EXPANDED WHO CASE DEFINITION FOR AIDS
An adult or adolescent(>12yrs) is considered to have AIDS if a test for HIV Ab
gives +ve result,and one or more of the following conditions are present

≥10% body wt loss or cachexia with diarrhoea or fever or both,intermittent or
constant,for atleast 1 month,not known to be due to a condition unrelated to
HIV infection

Cryptococcal meningitis

Pulmonary/extrapulmonary TB

Kaposi’s sarcoma

Neurological impairment

Candidiasis of esophagus

Clinically diagnosed life threatening or recurrent episodes of pneumonia with
or without etiological confirmation

Invasive cervical cancer

25. LABORATORY INVESTIGATIONS

Hematological investigations- anaemia of chronic
disease,neutropenia,lymphopenia(CD4+Tcell),thromb ocytopenia.Raised ESR.

p/s: atypical lymphocytes having a plasmacytoid appearance.

CD4+:CD8+T cells- ratio is reversed

Hypergammaglobulinemia : IgG & IgA levels raised

Lymph node biopsy -follicular hyperplasia

CSF- lymphocytic pleocytosis

26. HIV POSITIVITY

The presence of antibodies against HIV in human body is termed
HIV positivity & the person is called HIV positive

It takes 6-12 weeks after infection for antibodies to rise to
detectable levels.

So,there is a window period during which infected person may
transmit the infection despite being seronegative.

During this window period p24 antigen capture assays are useful

27. LABORATORY DIAGNOSIS OF HIV INFECTION

Methods utilized to detect:

Antibody

Antigen

Viral nucleic acid

Virus in culture

28. ELISA

Antibodies detected in ELISA include those directed against: p24, gp120,
gp160 and gp41, detected first in infection and appear in most individuals
Standard blood screening test

Sensitivity->99.5%


4th generation EIA test combine detection of Abs to HIV with detection of
p24 Ag for HIV

False positive EIA-

Abs to class II Ag

Auto antibodies

Hepatic disease

Recent influenza

Acute viral infections

So EIA confirmed by western blot, p24 Ag capture assay or HIV RNA tests.

29. WESTERN BLOT

Most popular confirmatory test

The following antigens must be present: p17, p24, p31, gp41,
p51, p55, p66, gp120 and gp160.

Antibodies to gp31, gp41, gp 120, and gp160 appear later but are
present throughout all stages of the disease.

Advantage-multiple antigens elicit production of specific
antibodies and can be detected as discrete bands on western blot

30. Interpretation of results.
No bands, negative.
In order to be
interpreted as positive a
minimum of 3 bands
directed against the
following antigens
must be present: p24,
p31, gp41 or
gp120/160.
CDC criteria require 2
bands of the following: p24,
gp41 or gp120/160

31. INDIRECT IMMUNOFLOURESCENCE

Can be used to detect both virus and antibody to it.

Antibody detected by testing patient serum against antigen applied
to a slide, incubated, washed and a fluorescent antibody added.

Virus is detected by fixing patient cells to slide, incubating with
antibody.

32. P24 ANTIGEN CAPTURE ASSAY

The p24-antigen screening assay is an EIA performed on serum or plasma.

P24 antigen only present for short time, disappears when antibody to p24
appears.

Greatest use as a screening test for persons suspected to have acute HIV
syndrome.

Test not recommended for routine screening as appearance and rate of
rise are unpredictable.

Sensitivity lower than ELISA.

33. 
Most useful for the following:

early infection suspected in seronegative patient

newborns

CSF

monitoring disease progress

34. CD4+ T CELL COUNT

Most widely used predictor of HIV progression.

Risk of progression to an AIDS opportunistic infection or
malignancy is high with CD4+T cell<200 cells/mcl

Percentage may be more reliable than CD4 count

Risk of progression to an AIDS opportunistic infection or
malignancy is high with percentage <20% in absence of treatment

35. 
Routine blood donor screening is done by nucleic acid testing.

3 assays are used where measurement of anti HIV Ab may be misleading—

RT-PCR

Branched DNA

Nucleic acid sequence based amplification (NASBA)

USE-

Diagnosis

Initial prognosis

Determining need for therapy

Monitoring effects of therapy

36. VIRUS ISOLATION

Virus isolation can be used to definitively diagnose HIV.

Best sample is peripheral blood, but can use CSF, saliva, cervical
secretions, semen, tears or material from organ biopsy.

Cell growth in culture is stimulated, amplifies number of cells
releasing virus.

Cultures incubated one month, infection confirmed by detecting
reverse transcriptase or p24 antigen in supernatant

37. VIRAL LOAD TEST






Viral load or viral burden is the quantity of HIV-RNA that is in the
blood.
RNA is the genetic material of HIV that contains information to
make more virus.
Viral load tests measure the amount of HIV-RNA in one milliliter of
blood.
Take 2 measurements 2-3 weeks apart to determine baseline.
Repeat every 3-6 months in conjunction with CD4 counts to
monitor viral load and T-cell count.
Repeat 4-6 weeks after starting or changing antiretroviral therapy
to determine effect on viral load.

38. TESTING OF NEONATES

Difficult due to presence of maternal IgG antibodies.

Use tests to detect IgM or IgA antibodies, IgM lacks sensitivity, IgA
more promising.

Measurement of p24 antigen.

PCR testing may be helpful but still not detecting antigen soon
enough: 38 days to 6 months to be positive

39. TESTING IN PREGNANT MOTHER

Screening to be done in 1st trimester of pregnancy

Maternal IgG crosses placenta & persists in infant blood for 15
mths.so standard EIA HIV serologic tests cannot be used to diagnose
infection in infant

IgM & IgA in infants are assayed (but not reliable in 1st 3 mths after
birth)

HIV DNA PCR- diagnostic at 1 mth of age

41. TREATMENT

Antiretroviral drugs target-protease,integrase,reverse transcriptase.

Highly active anti retroviral therapy( HAART )

Four approved classes of drugs in the HAART regimens
 Nucleoside and nucleotide reverse transcriptase inhibitors
 Non-nucleoside reverse transcriptase inhibitors
 Protease inhibitors
 Fusion inhibitors
Major causes of morbidity are-cancer,accelerated cardiovascular
diseases,kidney diseases and liver diseases.

42. PREVENTION

Monogamous Relationship

Protected Sex

Sterile needles

Proper screening of blood products before transfusion

43. THANK YOU