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Former Member
Cruncher Joined: May 22, 2018 Post Count: 0 Status: Offline |
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Former Member
Cruncher Joined: May 22, 2018 Post Count: 0 Status: Offline |
HIV funding cut as science brings 'decisive moment'
This year's World Aids Day comes at what many scientists and campaigners agree is a decisive moment in the 30-year history of the epidemic. Although there is still no vaccine against HIV, key trials in the past year have confirmed that the combination drug treatment makes people with HIV less infectious - and more men in Africa are being circumcised, to help prevent the virus being transmitted. But just as the science is bringing much-needed new results, funding is tailing off for the first time. |
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Former Member
Cruncher Joined: May 22, 2018 Post Count: 0 Status: Offline |
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Papa3
Senior Cruncher Joined: Apr 23, 2006 Post Count: 360 Status: Offline Project Badges: ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
http://www.futurity.org/health-medicine/new-a...s-more-potent-less-toxic/
http://dx.doi.org/10.1021/jm201134m YALE (US) — Researchers have discovered chemical compounds that could lead to HIV treatments that are 10 to 2,000 times more potent than drugs now on the market. [...] The new agents work by inhibiting the function of an enzyme essential for HIV’s replication. That enzyme is called HIV-1 reverse transcriptase. Classed as non-nucleoside reverse transcriptase inhibitors, the compounds prevent HIV from converting its genetic material into DNA, a necessary step for the infection of human cells. Two of the new agents are extraordinarily potent against the predominant, “wild-type” form of HIV, which is highly adept at mutation, according to the researchers. “The compound that we call JLJ494 is, I believe, one of the most potent compounds ever reported for inhibiting replication of wild-type HIV,” Jorgensen says. These agents could allow for comparatively lower dosages, and also for prophylactic anti-HIV treatment, he says. Importantly, they also show very low toxicity towards human cells. [...] The Jorgensen-Anderson team’s iterative approach, published in the Journal of Medicinal Chemistry, involved extensive computer modeling to design compounds that bind to the target enzyme. They then synthesized the most promising compounds and measured how they affected replication of the virus using live HIV and human T-cells. [...] |
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Papa3
Senior Cruncher Joined: Apr 23, 2006 Post Count: 360 Status: Offline Project Badges: ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
http://www.sciencecodex.com/read/changing_the...y_into_cell_nucleus-82858
Scientists have found the 'key' that HIV uses to enter our cells' nuclei, allowing it to disable the immune system and cause AIDS. [...] To access the DNA, the HIV must pass through the Nuclear Pore Complex, a gateway into the nucleus. Until now, the mechanism that allows the virus to pass through this gateway was unknown. [..] A part of the HIV virus called the capsid protein, acting like a key, binds to Nup358, a protein on the nuclear pore complex, unlocking the gateway and granting the virus access to the DNA. [...] |
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Former Member
Cruncher Joined: May 22, 2018 Post Count: 0 Status: Offline |
Seattle Scientists Inching Toward HIV Vaccine
The blog Seattle Weekly reports that scientists at the University of Washington are inching toward an HIV vaccine. Reportedly "This method uses two vaccine components -- a relatively harmless virus that delivers HIV proteins and primes the immune system, followed by booster shots of the HIV proteins themselves. This one-two punch approach activates both antibody and cell-mediated immune responses... " http://blogs.seattleweekly.com/dailyweekly/20...ng_toward_hiv_vaccine.php |
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Dan60
Senior Cruncher Brazil Joined: Mar 29, 2006 Post Count: 185 Status: Offline Project Badges: ![]() ![]() ![]() ![]() |
Two Major Pharmaceutical Companies Take the Lead for an HIV Cure
"...Romas Geleziunas from Gilead (Foster City, USA) and Roger Sutmuller from Tibotec Janssen (Antwerp, Belgium) clearly showed that finding a cure was a top priority in their agenda." http://www.hiv-reservoir.net/index.php/the-ne...lead-for-an-hiv-cure.html |
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Michael2901
Veteran Cruncher Joined: Feb 6, 2009 Post Count: 586 Status: Offline Project Badges: ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
http://www.medicalnewstoday.com/releases/239199.php
"Article Date: 16 Dec 2011 Immune Cells Exhausted By Chronic Viral Infection Can Be Revived Chronic infections by viruses such as HIV or hepatitis C eventually take hold because they wear the immune system out, a phenomenon immunologists describe as exhaustion. Yet exhausted immune cells can be revived after the introduction of fresh cells that act like coaches giving a pep talk, researchers at Emory Vaccine Center have found. Their findings provide support for an emerging strategy for treating chronic infections: infusing immune cells back into patients after a period of conditioning. The results are published this week in Proceedings of the National Academy of Sciences Early Edition..." |
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Michael2901
Veteran Cruncher Joined: Feb 6, 2009 Post Count: 586 Status: Offline Project Badges: ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
http://www.medicalnewstoday.com/releases/239230.php
"Article Date: 16 Dec 2011 New Hope In Fight Against Global HIV/AIDS Pandemic Scientists at the Gladstone Institutes have discovered new protein fragments in semen that enhance the ability of HIV, the virus that causes AIDS, to infect new cells - a discovery that one day could help curb the global spread of this deadly pathogen. HIV/AIDS has killed more than 25 million people around the world since first being identified some 30 years ago. In the United States alone, more than one million people live with HIV/AIDS at an annual cost of $34 billion. Previously, scientists in Germany discovered that HIV transmission is linked to the presence of an amyloid fibril in semen. This fibril - a small, positively charged structure derived from a larger protein - promotes HIV infection by helping the virus find and attach to its target: CD4 T white blood cells. In Cell Host & Microbe, researchers in the laboratory of Warner C. Greene, MD, PhD, who directs virology and immunology research at Gladstone, describe a second type of fibril that also has this ability. These findings may spur efforts to slow the spread of HIV/AIDS. Prevention has recently focused on microbicides; chemical gels that, when used by women during sexual intercourse, block HIV infection. But while early microbicides had some success - reducing infection by an average of 39% - more recent trials have failed and devising a truly potent microbicide remains a top priority. "Today's microbicides may be failing because, while they do target the virus itself, they don't block the virus from interacting with the natural infection-enhancing components of semen," said Nadia R. Roan, PhD, the paper's first author and a research scientist at Gladstone, an independent and nonprofit biomedical-research organization. "Now that we more fully understand how HIV hijacks these components to promote its own infection, we are one step closer to developing a microbicide that can more effectively stop HIV."... |
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Michael2901
Veteran Cruncher Joined: Feb 6, 2009 Post Count: 586 Status: Offline Project Badges: ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
http://www.sciencedaily.com/releases/2011/09/110919151306.htm
"Shark Compound Proves Potential as Drug to Treat Human Viruses, Says Researcher ScienceDaily (Sep. 19, 2011) — A compound initially isolated from sharks shows potential as a unique broad-spectrum human antiviral agent, according to a study led by a Georgetown University Medical Center investigator and reported in the Proceedings of the National Academy of Sciences Early Edition online Sept. 19. The compound, squalamine, has been in human clinical trials for the treatment of cancer and several eye disorders, and so has a well-known safety profile, suggesting it can be quickly tested as a new class of drugs to treat infections caused by viruses ranging from dengue and yellow fever to hepatitis B, C, and D. In both lab and animal experiments, the compound effectively demonstrated antiviral activity against these human pathogens, some of which cannot now be effectively treated. "To realize that squalamine potentially has broad antiviral properties is immensely exciting, especially since we already know so much from ongoing studies about its behavior in people," says the study's lead investigator, Michael Zasloff, M.D., Ph.D., professor of surgery and pediatrics at Georgetown University Medical Center and scientific director of the Georgetown Transplant Institute. Not only does the study offer a promising clinical advance, Zasloff might have answered the longstanding mystery of how sharks, which have a very primitive immune system, can so effectively fight the viruses that plague all living creatures. "I believe squalamine is one of a family of related compounds that protects sharks and some other 'primitive' ocean vertebrates, such as the sea lamprey, from viruses," he says. "Squalamine appears to protect against viruses that attack the liver and blood tissues, and other similar compounds that we know exist in the shark likely protect against respiratory viral infections, and so on. "We may be able to harness the shark's novel immune system to turn all of these antiviral compounds into agents that protect humans against a wide variety of viruses," Zasloff says. "That would be revolutionary. While many antibacterial agents exist, doctors have few antiviral drugs to help their patients, and few of those are broadly active."... |
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