Download Free Medical Anti-HIV Drugs PowerPoint Presentation

Anti-HIV Drugs PowerPoint Presentation

DOWNLOAD MEDICAL POWERPOINT PRESENTATION

About This Presentation

Description : This medical presentation titled ""Anti-HIV Drugs"" is about Anti-HIV Drug or antiretroviral drugs.

Tags : Human Immunodeficiency Virus, HIV, infection, cells, immune system, AIDS, Acquired Immune Deficiency Syndrome, HIV Positive, Anti-HIV Drug, antiretroviral drugs, AIDS drugs, HIV Protease, Alternative Therapies, therapy

Published on : Apr 22, 2021 | Views : 2338 | Downloads : 7

Shareable Url :

Embed Code :

Comment

Transcript

Slide 1-

Anti-HIV Drugs Cathy Molina
Slide 2-

Some HIV Facts HIV – the Human Immunodeficiency Virus is the retrovirus that causes AIDS HIV belongs to the retrovirus subfamily lentivirus. HIV attaches to cells with CD4 receptors (T4 cells and macrophages).
Slide 3-

HIV Life Cycle1 Step 1: Attachment of virus at the CD4 receptor and chemokine co-receptors CXCR4 or CCR5 Step 2: viral fusion and uncoating Steps 3-5: Reverse transcriptase makes a single DNA copy of the viral RNA and then makes another to form a double stranded viral DNA Step 6: migration to nucleus Steps 7-8: Integration of the viral DNA into cellular DNA by the enzyme integrase Steps 9-11: Transcription and RNA processing Steps 12-13: Protein synthesis Step 14: protease cleaves polypeptides into functional HIV proteins and the virion assembles Step 15: virion budding Step 16: Virion maturation
Slide 4-

Anti- HIV Drug Targets2 Three types of drugs are currently in clinical use: nucleoside and nucleotide reverse transcriptase (RT) inhibitors non-nucleoside reverse transcriptase inhibitors protease inhibitors (PIs)
Slide 5-

Nucleoside and Nucleotide Analogs Nucleoside analogs (NRTI) act as chain terminators or inhibitors at the substrate binding site of RT NRTI’s must be phosphorylated (three steps) to their 5’-triphosphate form to become active inhibitors. Nucleotide analogs (NtRTI) already contain a phosphate group and only go through 2 steps to become active. The 5’-triphosphate of the NRTI’s compete with the 2’-deoxynucleoside’s 5’-triphosphate for binding to reverse transcriptase leading to viral DNA chain termination3.
Slide 6-

Nucleoside Analogs There are currently 7 FDA-approved NRTI’s and one nucleotide analog. The first anti-HIV drug approved was the NRTI known as AZT or Zidovudine (1987). AZT was discovered as a treatment of AIDS during a screening process for the identification of effective AIDS treatments4. Antiviral selectivity due to higher affinity for HIV RT than human DNA polymerases.
Slide 7-

Non-Nucleoside Analogs Non-nucleoside analog reverse transcriptase inhibitors (NNRTI’s) inhibit viral DNA replication by binding at the allosteric non-bonding site of RT, causing a conformational change of the active site. NNRTI’s do not require bioactivation by kinases. Three NNRTI’s are currently approved for clinical use in combination therapy: nevirapine, delavirdine, and efavirenz
Slide 8-

Non-Nucleoside Analogs5 Delavirdine Benzoxazinone Nevirapine
Slide 9-

Protease Inhibitors During the reproduction cycle of HIV a specific protease is needed to process GAG and POL polyproteins into mature HIV components. If protease is missing noninfectious HIV is produced. HIV protease inhibitors are specific to HIV protease because it differs significantly from human protease. The 6 PI’s currently approved for clinical use were all designed by using structure-based drug design methods4.
Slide 10-

HIV Protease6 The crystal structure of HIV protease was first obtained at Merck Laboratories. HIV protease is a 99 amino acid aspartyl protease that functions as a homodimer with one active site. The active sites of protease are hydrophobic.
Slide 11-

Protease Inhibitors7 HIV PI’s target the peptide linkages in the gag and gag-pol polyproteins which must be cleaved by protease. All approved PI’s contain a hydroxyethylene bond instead of a normal peptide bond. The hydroxyethylene bond makes PI’s non-scissile substrate analogs for HIV protease
Slide 12-

Protease Inhibitors7 ABT-378 or lopinavir was approved in 2000 for use in combination with ritonavir (a PI) (Kaletra) Ritonavir strongly inhibits the metabolism of ABT-378
Slide 13-

Some Alternative Therapies Virus adsorption inhibitors – interfere with virus binding to cell surface by shielding the positively charged sites on the gp-120 glycoprotein Polyanionic compounds Viral coreceptor antagonists – compete for binding at the CXCR4 (X4) and CCR5 (R5) coreceptors bicyclams and ligands
Slide 14-

Virus Adsorption Inhibitors Cosalane was originally developed as an anti-cancer agent by researchers at Purdue University and the U.S. National Cancer Institute8. Cosalane was developed from a chemical known as ATA (aurintricarboxylic acid), which has long been known to have anti-HIV activity8. ATA is a mixture of different polymers. Chemists took one of the low molecular weight components of ATA, and attached it to a steroid molecule in order to target the substance more effectively to the surface of viruses and of cells. The result was cosalane. Cosalane binds to the HIV gp-120 protein.
Slide 15-

Viral Coreceptor Antagonists Bicyclams are a type of viral coreceptor antagonist. They are very specific and potent X4 coreceptor antagonists. Bicyclams belong to a class of macrocyclic polyamines consisting of two cyclam units linked by an aliphatic bridge Bicyclams with an aromatic linker apparently had higher antiviral activity10. One such compound is AMD3100.
Slide 16-

Combination Therapy Combination therapy often called HAART is standard care for people with HIV. Monotherapy created virus resistance to the individual drug. Some combination therapies increase the time it takes for the virus to become resistant. Combinations of a PI or NNRTI with one or two NRTI’s is often recommended. Combination therapy may reduce individual drug toxicity by lowering the dosage of each drug
Slide 17-

Combination Therapy The combination of drugs chosen is based on the history of each individual patient and synergistic drug interactions. Some drugs compete with each other for binding sites or enzymes. Example: zidovudine and stavudine both nucleoside analogs compete for the same kinase. Stavudine is not phosphorylated because zidovudine is preferred5.
Slide 18-

Combination Therapy and Drug Resistance Some drug combinations can restore sensitivity of the virus to drugs it was previously resistant to. Example: lamivudine and zidovudine The HIV M184V mutation is resistant to lamivudine but restores sensitivity to zidovudine resistant virus mutants5.
Slide 19-

Drug Toxicity and Side Effects All available antiretroviral drugs are toxic. Side effects of nucleoside analogs are lactic acidosis and severe hepatomegaly with steatosis (enlarged fatty liver)11. Other side effects of anti-HIV drugs include pancreatitis, myopathy, anemia, peripheral neuropathy, nausea, and diarrhea.
Slide 20-

Reducing Drug Toxicity The use of combination therapy: Combining agents with favorable synergistic properties allows a decrease in dose or dosing frequency Ritonavir alone cause gastrointestinal side effects but when used in combination with other PI’s it can be administered at a lower dose.
Slide 21-

Conclusions An effective anti-HIV therapy is still needed. Several possible targets are being studied and tested. The area of anti-HIV drugs has more room for growth and the future for the discovery of new effective drugs is promising.
Slide 22-

References NIAID HIV Life Cycle. http://www.niaid.nih.gov/daids/dtpdp/virpage1.htm (accessed Oct 2004). De Clerq, E. New anti-HIV agents and targets. Med. Res. Rev. 2002, 22(6), 531-565. El Kouni, M. H. Trends in the design of nucleoside analogues as anti-HIV drugs. Current Pharmaceutical Design. 2002, 8(8), 581-593. Block, J. H.; Beale, J. M. Antiviral Agents, Wilson and Gisvold’s Textbook of Organic Medicinal and Pharmaceutical Chemistry, 11th ed; Lippincott Williams & Wilkins: Maryland, 2004; pgs 379, 943. De Clerq, E.; Vandamme, A-M. Combination Therapy of AIDS. Birkhauser Verlag: Germany, 2004. Brik, A.; Wong, C-H. HIV-1 protease: mechanism and drug discovery. Organic & Biomolecular Chemistry. 2003, 1(1), 5-14. De Clerq, E. New Developments in Anti-HIV Chemotherapy. Current Medicinal Chemistry. 2001, 8, 1543-1572. cosalane website – look up Ruell, J. A.; De Clercq, E.; Pannecouque, C. Synthesis and Anti-HIV Activity of Cosalane Analogues with Substituted Benzoic Acid Rings Attached to the Pharmacophore through Methylene and Amide Linkers. J. Org. Chem. 1999, 64, 5858-5866. Labrosse, B.; Brelot, A.; Heveker, N.; Sol, N. Determinants for Sensitivity of Human Immunodeficiency Virus Coreceptor CXCR4 to the Bicyclam AMD3100. J. Virol. 1998, 6381–6388. Simple FactSheet from the AIDS Treatment Data Network. http://www.atdn.org/simple/abac.html (accssed Nov 2004).