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HIV
Characteristics of the virus
Characteristics of the virus
Icosahedra (20 sided), enveloped virus of the lentivirus subfamily of retroviruses.
Two viral strands of RNA found in core surrounded by protein outer coat. Outer envelope contains a lipid matrix within which
specific viral glycoproteins are imbedded. These knob-like structures responsible for binding to
target cell.
HIV
• HIV is a RETROVIRUS. A Retrovirus is a ribonucleic acid (RNA) virus that must reverse to the Deoxyribonucleic acid (DNA) before reproducing/replicating.• It is the DNA gene that enables the Virus to replicate. HIV invades mainly the helper T cells to replicate itself.• No Cure
prevalence
prevalence Estimated HIV/AIDS prevalence among young adults (15-49) by country as of 2008.
Stage 1 - Primary
Short, flu-like illness - occurs one to six weeks after infection
no symptoms at all Infected person can infect other people
Stage 2 - Asymptomatic Lasts for an average of ten years This stage is free from symptoms There may be swollen glands The level of HIV in the blood drops to very
low levels HIV antibodies are detectable in the blood
Stage 3 - Symptomatic
The symptoms are mild The immune system deteriorates emergence of opportunistic infections and cancers
Stage 4 - HIV AIDS
The immune system weakens
The illnesses become more severe leading to an AIDS diagnosis
Opportunistic Infections associated with AIDS
BacterialTuberculosis (TB)Strep pneumonia
ViralKaposi SarcomaHerpesInfluenza (flu)
Opportunistic Infections associated with AIDSParasitic
Pneumocystis carinii
FungalCandidaCryptococcus
HIV/AIDS Transmission
Sexual Blood products
Mother-to-child Multiple infection
Transmission
Life Cycle of HIV There are 7 steps in the life cycle of HIV, they
are Binding, Reverse transcription, Integration, Transcription, Translation, Assembly, Budding.
Treatment When several such drugs, typically three
or four, are taken in combination, the approach is known as Highly Active Antiretroviral Therapy, or HAART.
The decision on when to start treatment should take into account , HIV viral load, treatment history, resistance profiles and patient preference.
Ann. Intern. Med. 137 (5 Pt 2): 381–433. PMID 12617573
APPROACHES FOR TREATMENT OF AIDS
NATURAL ANTI HIV AGENTS CHEMOKINE (CCR5 and CXCR4) RECEPTOR
ANTAGONIST ANTI-SENSE OLIGONUCLEOTIDES ANTI-CD4 MONOCLONAL ANTIBODY TNX -
355 NANOTECHNOLOGY FOR HIV/AIDS
TREATMENT MEDICINAL CHEMISTRY FOR THE
TREATMENT OF AIDS
Classes of drugs
Antiretroviral (ARV) drugs are broadly classified by the phase of the retrovirus life-cycle that the drug inhibits.
Reverse-transcriptase inhibitor(RTI) Protease inhibitors (PIs) Integrase inhibitors Entry inhibitors (or fusion inhibitors) Maturation inhibitors
Reverse-transcriptase inhibitor
RTIs come in three forms: Nucleoside analog reverse-transcriptase
inhibitors (NARTIs or NRTIs) Nucleotide analog reverse-transcriptase
inhibitors (NtARTIs or NtRTIs) Non-nucleoside reverse-transcriptase
inhibitors (NNRTIs)
Mechanism
When HIV infects a cell, reverse transcriptase copies the viral single stranded RNA genome into a double-stranded viral DNA. The viral DNA is then integrated into the host chromosomal DNA, which then allows host cellular processes, such as transcription and translation to reproduce the virus. RTIs block reverse transcriptase's enzymatic function and prevent completion of synthesis of the double-stranded viral DNA, thus preventing HIV from multiplying
Zidovudine(Azidothymidine,AZT) AZT was the first approved treatment for HIV,
sold under the names Retrovir and Retrovis. AZT use was a major breakthrough in AIDS
therapy in the 1990s. AZT slows HIV spread significantly, but does not
stop it entirely.
World Health Organization. March 2005. Retrieved 2006-03-12
Tenofovir
Tenofovir disoproxil fumarate (TDF or PMPA), marketed by Gilead Sciences under the trade name Viread, belongs to a class of antiretroviral drugs known as nucleotide analogue reverse transcriptase inhibitors (NRTIs), which block reverse transcriptase, an enzyme crucial to viral production in HIV-infected people.
Emau P, Jiang Y, Agy MB, et al. (2006).
Efavirenz brand names Sustiva and Stocrin NNRTI Unlike NRTIs, which bind at the enzyme's active
site, NNRTIs act allosterically by binding to a distinct site away from the active site known as the NNRTI pocket.
Ren J, Bird LE, Chamberlain PP, et al. (2002). "Structure of HIV-2 reverse transcriptase at 2.35-A resolution and the mechanism of resistance to non-nucleoside inhibitors". Proc Natl Acad Sci USA 99 (22): 14410–15. doi:10.1073/pnas.222366699. PMID 12386343
Protease inhibitors (PIs)
PIs prevent viral replication by inhibiting the activity of proteases
Protease inhibitors were the second class of antiretroviral drugs developed.
Rang, H. P., Dale, M. M., Ritter, J. M., & Flower, R. J. (2007). Rang and Dale's Pharmacology (6th Edition ed.). Philadelphia: Churchill Livingstone Elsevier.
Saquinavir Saquinavir was the first protease inhibitor (and
sixth antiretroviral) approved by the Food and Drug Administration (FDA).
HIV protease is vital for both viral replication within the cell and release of mature viral particles from an infected cell. Saquinavir inhibits both HIV-1 and HIV-2 proteases.
FortovaseTM (saquinavir) soft gelatin capsules. Product information (November 1997)
Integrase inhibitor
Integrase inhibitors are a class of antiretroviral drug designed to block the action of integrase, a viral enzyme that inserts the viral genome into the DNA of the host cell.
Steigbigel RT, Cooper DA, Kumar PN, et al. (July 2008).
Raltegravir Raltegravir (MK-0518, brand name Isentress) Raltegravir targets integrase, an HIV enzyme
that integrates the viral genetic material into human chromosomes, a critical step in the pathogenesis of HIV. The drug is metabolized away via glucuronidation
Savarino A (December 2006). "A historical sketch of the discovery and development of HIV-1 integrase inhibitors". Expert Opin Investig Drugs 15 (12): 1507–22.
Entry inhibitor Entry inhibitors, also known as fusion inhibitors This class of drugs interferes with the
binding, fusion and entry of an HIV virion to a human cell. By blocking this step in HIV's replication cycle, such agents slow the progression from HIV infection to AIDS
An HIV virion binds to a CD4+ human cell. The two bottom pictures depict two proposed models of HIV fusion with the cell.
Biswas P, Tambussi G, Lazzarin A (2007). "Access denied? The status of co-receptor inhibition to counter HIV entry" (abstract page). Expert Opin Pharmacother 8 (7): 923–33. doi:10.1517/14656566.8.7.923. PMID 17472538
Proteins involved in the HIV entry process.
CD4, a protein receptor found on the surface of helper T cells in the human immune system, also called CD4+ T cells
gp120, a protein on HIV surface that binds to the CD4 receptor
CCR5, a second receptor found on the surface of CD4+ cells, called a chemokine co-receptor
CXCR4, another chemokine co-receptor found on CD4+ cells "parang gago"
gp41, a HIV protein, closely associated with gp120, that penetrates the cell membrane
Maraviroc brand-named Selzentry, or Celsentri outside the U.S. Maraviroc is an entry inhibitor. Specifically, maraviroc is
a CCR5 receptor antagonist, and binds to the chemokine receptor CCR5 and blocks the HIV gp120 (V3 loop) from associating with the receptor. HIV is then unable to bind and enter human macrophages.
Levy JA (January 2009). "HIV pathogenesis: 25 years of progress and persistent challenges". AIDS 23 (2): 147–60. doi:10.1097/QAD.0b013e3283217f9f. PMID 19098484
CCR5-receptor antagonists
Figure 1 HIV entry into CD4+ cell via CCR5 co-receptor.
Maturation inhibitor
Maturation inhibitors inhibit the last step in gag processing in which the viral capsid polyprotein is cleaved, thereby blocking the conversion of the polyprotein into the mature capsid protein. Because these viral particles have a defective core, the virions released consist mainly of non-infectious particles. Alpha interferon is a currently available agent in this class. Two additional ones under investigation are bevirimat and Vivecon.
Alpha Interferon
Interferons (IFNs) are proteins made and released by lymphocytes in response to the presence of pathogens—such as viruses, bacteria, or parasites—or tumor cells.
Liu YJ (2005). "IPC: professional type 1 interferon-producing cells and plasmacytoid dendritic cell precursors". Annu Rev Immunol 23: 275–306.
The Move Toward Lower Pill BurdensDosing Daily pill burdenRegimen
1996
Zerit/Epivir/Crixivan 10 pills, Q8H
20023 pills, BIDCombivir (AZT/3TC)/EFV
1998Retrovir/Epivir/Sustiva 5 pills, BID
20033 pills, QDViread/ Emtriva/Sustiva
20042 pills, QDTruvada/Sustiva
Reading:
Thakur, D. S. et al. “Anti-HIV Agents: A Step Toward Future” International Journal of Pharmaceutical Sciences Review and Research (2010) Vol. 3, pp. 10-18.
Questions: Q: What is the ETIOLOGY of AIDS? Q: How many steps are there in the life cycle of HIV and what
are they? Q: What is CCR5 and how it relates with HIV? Q: In natural anti HIV agents, what structure does prostratin
have and where does it comes from and how it possibly works? Q: How does maraviroc works to treat HIV? Q: Give two example of structure of classical antiretroviral
agents, and what function group do you think is they have in common?