new drug therapy in the treatment of AIDS, cancer
Try Our Service! Get Free Quote Now!
There is no other field of medicine that has been through such dramatic developments as that of antiretroviral therapy . In September 1995 , the results of Eurpean-Australian DELTA study , and the American ACTG pointed out that two nucleoside analogues were more effective than monotherapy .This led to the belief , thatlonger survival was possible in HIV .Protease inhibitors (PIs ) came about in 1995 , and in June 1996 , the first non-nucleoside reverse transcriptase inhibitor (NNRTI ) neviparine arrived , and so did Nelfinavir which was a new PIs . This led to the start of HAART (Highly Active Anti-Retroviral Therapy .Antiretroviral drugs have been divided into a number of groups on the basis of the phase of the retrovirus life-cycle that the drug inhibits .1 Nucleoside nucleotide reverse transcriptase inhibitors (NRTI )inhibit reverse transcription by incorporating into the newly synthesized viral DNA and slowing its elongation . Apricitabine (AVX-754 )is a heterocyclic cytidine analog , which may enter the market in 2009 .Elvucitabine is currently in phase II trials . Stampidine is 100 times more potent than AZT and has potential role against HIV mutants 2 Non-nucleoside reverse transcriptase inhibitors (nNRTI ) inhibit reverse transcriptase directly by binding to the enzyme and not allowing its function . Efavirenz has been the agent that has been most successful , but is facing lot of viral resistance . Rilpivarine has a long half life of 40 hours .3 Protease inhibitors (PIs ) target viral architecture by inhibiting the activity of protease , an enzyme used by the virus to form new virons from the older protein framework . PL-100 is given as a prodrug and is active against multi PIs resistant strains . It has a long half life of 37 hours , and can act as a co-drug .4 Integrase inhibitors inhibit the enzyme integrase (integrates viral DNA into DNA of the infected cell . Raltegravir became the first to receive FDA approval in October 2007 . it is the most exciting of all anti HIV agents in the market . It acts against HIV-2 also . Elvitegasir has a potential as monotherapy .5 Entry inhibitors (or fusion inhibitors ) prevent the binding , fusion and entry of HIV-1 virus into the host cell . It acts via the gp 120 envelope protein to the CD 4 receptor . Maraviroc and enfuvirtide are marketed agents of this group .6 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 (p24 .These virons are thus incomplete and thus uninfective . Two drugs in this group are under investigation , bevirimat ,`and Vivecontm .7 . Immunotherapy . IL-2 is a cytokine from the activated T – cells ,which induces proliferation in T , B , and NK cells . It causes an increase in CD 4 and CD 8 cells . It is useful in patients with poor immunological response to antiretroviral therapy to stimulate the immune system .G-CSF , GM CSF are used for treatment of prolonged neutropenia in patients with advanced HIV infection to reduce bacterial infection .Why is treatment of HIV difficult ?The retrovirus has an extremely…

