Showing posts with label AIDS. Show all posts
Showing posts with label AIDS. Show all posts

The effect of smallpox and BCG vaccination on the risk of HIV-1 infection in Guinea-Bissau and Denmark | Open Forum Infectious Diseases | Oxford Academic

Background:
The live smallpox and BCG vaccinations have been associated with better adult survival in both Guinea-Bissau and Denmark. In Guinea-Bissau, HIV-1 became an important cause of death after smallpox vaccination was phased out globally in 1980. We hypothesised that smallpox and BCG vaccinations were associated with a lower prevalence of HIV-1 infection, and tested this hypothesis both in Guinea-Bissau and in Denmark.

Methods:
We conducted two studies, a cross-sectional study of HIV infection and vaccination scars in Guinea-Bissau including 1,751 individuals, and a case-base study with a background population of 46,239 individuals in Denmark. In Guinea-Bissau, HIV-1 transmission is almost exclusively sexually transmitted, in Denmark we excluded intravenous drug users. Data was analysed using logistic regression.

Results:
BCG and/or smallpox vaccination compared with neither of these vaccines was associated with an adjusted odds ratio (aOR) for HIV-1 of 0.62 (95% confidence interval (CI) 0.36-1.07) in Guinea-Bissau and 0.70 (95%CI 0.43-1.15) in Denmark. Combining results from both settings in a meta-analysis gave an aOR of 0.66 (95%CI 0.46-0.96). Data from Guinea-Bissau indicated a stronger effect of multiple smallpox vaccination scars (aOR of 0.27 (95%CI 0.10-0.75); women: 0.18 (95%CI 0.05-0.64), men: 0.52 (95%CI 0.12-2.33), sex-differential effect, p-value = 0.29).


Conclusions:
The studies from Guinea-Bissau and Denmark, two very different settings, both suggest that the BCG and smallpox vaccines could be associated with a decreased risk of sexually transmitted HIV-1. It might be informative to pursue this observation and explore possible protective mechanisms as part of the search for an HIV-1 vaccine."


Related:- Cowpox Helped Against Smallpox; Will the Goat Lentivirus (Caprine Arthritis Encephalitis Virus) Help Against HIV-1?

Vaccinia and other viruses with available vaccines show marked homology with the HIV-1 envelope glycoprotein: the prospect of using existing vaccines to stem the AIDS pandemic.

RNA-directed gene editing specifically eradicates latent and prevents new HIV-1 infection

For more than three decades since the discovery of HIV-1, AIDS remains a major public health problem affecting greater than 35.3 million people worldwide. Current antiretroviral therapy has failed to eradicate HIV-1, partly due to the persistence of viral reservoirs. RNA-guided HIV-1 genome cleavage by the Cas9 technology has shown promising efficacy in disrupting the HIV-1 genome in latently infected cells, suppressing viral gene expression and replication, and immunizing uninfected cells against HIV-1 infection. These properties may provide a viable path toward a permanent cure for AIDS, and provide a means to vaccinate against other pathogenic viruses. Given the ease and rapidity of Cas9/guide RNA development, personalized therapies for individual patients with HIV-1 variants can be developed instantly.

BBC News - Immune upgrade with CCR5 delta gives 'HIV shielding'

researchers at the University of Pennsylvania are adapting patients' own immune systems to give them the defence offered by the CCR5 delta chemokine receptor .
Millions of T-cells were taken from the blood and grown in the laboratory until the doctors had billions of cells to play with.
The team then edited the DNA inside the T-cells to give them the shielding mutation - known as CCR5-delta-32.
About 10 billion cells were then infused back in, although only around 20% were successfully modified.
When patients were taken off their medication for four weeks, the number of unprotected T-cells still in the body fell dramatically, whereas the modified T-cells seemed to be protected and could still be found in the blood several months later.

BBC News - Body's anti-HIV 'training manual' offers vaccine hopes

The body's own "training manual" for successfully attacking HIV has been recorded by scientists and it is hoped it can be used to design vaccines.

Innate immune system can kill HIV when a viral gene is deactivated

 "A family of human proteins called APOBEC3 effectively restrict the growth of HIV and other viruses, but this action is fully counteracted by the viral infectivity factor gene (vif) in HIV. In the study, researchers intravenously infected humanized mice with HIV. They found that the most commonly transmitted strains of HIV are completely neutralized by APOBEC3 proteins when vif is removed from the virus.
"Without the vif gene, HIV can be completely destroyed by the body's own immune system," said J. Victor Garcia, PhD, professor of medicine at the UNC School of Medicine and senior author on the study. "These results suggest a new target for developing drugs fully capable of killing the virus.""


A 'Neurosteroid' Found To Prevent Brain Injury Caused By HIV/AIDS

MNT: A team of scientists from Canada, Thailand and Morocco have found that DHEA-S may prevent neurocognitive impairment that affects a significant percentage of AIDS patients. In a report appearing in the February 2013 issue of The FASEB Journal, they describe how a network of steroid molecules found in the brain, termed "neurosteroids," is disrupted during HIVinfection leading to brain damage. This suggests that treatment with one of these steroid molecules, called DHEA-S, may offset the disruption caused by the virus to prevent or reduce brain damage. 

Australian scientists may have found ‘potential cure for Aids’ Microbe World

A FORM of gene therapy developed by researchers at the Queensland Institute of Medical Research may provide hope to sufferers of HIV, preventing the virus from crippling the immune system by manipulating its genetic structure and turning HIV into a weapon against itself.

SIV and the Expanding Virome - The Scientist Magazine®

Pathogenic infection with simian immunodeficiency virus (SIV), a relative of HIV that infects non-human primates, is associated with increased diversity of gastrointestinal virus species in rhesus macaques, according to findings published today (October 11) in Cell. Though previous work has implicated intestinal bacteria in stimulating chronic inflammation, which is believed to promote progression from HIV or SIV infection to AIDS, the new findings suggest that gut viruses may also play a role.

New Clue To Slower Progression Of AIDS: MNT

The average time from HIV infection to full-blown AIDS in the absence of treatment is about 10 years, and while some people succumb much sooner, others, known as the "slow progressors", can remain healthy for another 20 years or more. Now scientists at the University of California, Los Angeles (UCLA), believe they may have uncovered a new clue as to why.

Anti-interferon-gamma autoantibodies cause adult-onset immunodeficiency disease similar to patients with advanced HIV infection | The Virology Hub

Work by Browne, S. K. et al (2012) showed that anti–interferon (IFN)-gamma autoantibodies found in a group of Asian adults with disseminated nontuberculous mycobacterial infection, alone or with another opportunistic infection, had an adult-onset immunodeficiency disease similar in nature to that seen in patients with advanced HIV infection. The cause of the anti-interferon-gamma autoantibodies appeared unrelated to a singular genetic predisposition and the authors speculate that an environmental factor or opportunistic infection could be the trigger.

New research helps explain why AIDS vaccine has been so difficult to develop

For decades, a successful HIV vaccine has been the Holy Grail for researchers around the globe. Yet despite years of research and millions of dollars of investment, that goal has still yet to be achieved. Recent research by Oregon Health & Science University scientists explains a decades-old mystery as to why slightly weakened versions of the monkey AIDS virus were able to prevent subsequent infection with the fully virulent strain, but were too risky for human use, and why severely compromised or completely inactivated versions of the virus were not effective at all.

Read more at: http://medicalxpress.com/news/2012-09-aids-vaccine-difficult.html#jCp

A safer strategy for targeting AIDS

Scientists at The Scripps Research Institute have discovered a surprisingly simple and safe method to disrupt specific genes within cells. The scientists highlighted the medical potential of the new technique by demonstrating its use as a safer alternative to an experimental gene therapy against HIV infection.The new technique, reported last month in the journal Nature Methods, employs zinc finger nuclease (ZFN) proteins, which can bind and cut DNA at precisely defined locations in the genome. ZFNs are coming into widespread use in scientific experiments and potential disease treatments, but typically are delivered into cells using potentially risky gene therapy methods.
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MicrobeWorld - Cancer drug shocks HIV out of hiding

Awakening the virus from its hiding place may allow its attack and elimination ...........

Bone marrow transplant eliminates signs of HIV infection

Two men with longstanding HIV infections no longer have detectable HIV in their blood cells following bone marrow transplants. The virus was easily detected in blood lymphocytes of both men prior to their transplants but became undetectable by eight months post-transplant. The men, who were treated at Brigham and Women's Hospital (BWH), have remained on anti-retroviral therapy. Their cases will be presented on July 26, 2012 at the International AIDS Conference by Timothy Henrich, MD and Daniel Kuritzkes, MD, physician-researchers in the Division of Infectious Diseases at BWH.

Futurity.org – Sea moss compound flushes out latent HIV

STANFORD (US) — A new collection of compounds—derived from a tiny marine organism—activate hidden reservoirs of HIV that currently make AIDS nearly impossible to eradicate.

Breast milk kills HIV and blocks its oral transmission in humanized mouse

More than 15 percent of new HIV infections occur in children. Without treatment, only 65 percent of HIV-infected children will live until their first birthday, and fewer than half will make it to the age of two. Although breastfeeding is attributed to a significant number of these infections, most breastfed infants are not infected with HIV, despite prolonged and repeated exposure.

Immune cells in the gut may improve control of HIV growth

The findings of a new study in monkeys may help clarify why some people infected with HIV are better able to control the virus. They also may pinpoint a target for treatment during early HIV infection aimed at increasing the supply of certain immune cells in the gut, which the study shows could be an important factor in limiting HIV growth in cells throughout the body.

Revealed: Secret of HIV's natural born killers

Only about one person in 300 has the ability to control the human immunodeficiency virus (HIV) without drugs, using a strain of "killer" cells called cytotoxic T lymphocyte (CTL) cells, previous research has found.Taking that discovery further, scientists from the United States, Canada, Japan and Germany reported that the strain has molecules called receptors that are better able to identify HIV-infected white blood cells for attack.
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Newly discovered breast milk antibodies help neutralize HIV

Antibodies that help to stop the HIV virus have been found in breast milk. Researchers at Duke University Medical Center isolated the antibodies from immune cells called B cells in the breast milk of infected mothers in Malawi, and showed that the B cells in breast milk can generate neutralizing antibodies that may inhibit the virus that causes AIDS.

Unveiling the mechanisms for decreased glutathione in individuals with HIV infection.

We examined the causes for decreased glutathione (GSH) in individuals with HIV infection. We observed lower levels of intracellular GSH in macrophages from individuals with HIV compared to healthy subjects. Further, the GSH composition found in macrophages from HIV(+) subjects heavily favors oxidized glutathione (GSSG) which lacks antioxidant activity, over free GSH which is responsible for GSH's antioxidant activity. This decrease correlated with an increase in the growth of Mycobacterium tuberculosis (M. tb) in macrophages from HIV(+) individuals. In addition, we observed increased levels of free radicals, interleukin-1 (IL-1), interleukin-17 (IL-17) and transforming growth factor-β (TGF-β) in plasma samples derived from HIV(+) individuals compared to healthy subjects. We observed decreased expression of the genes coding for enzymes responsible for de novo synthesis of GSH in macrophages derived from HIV(+) subjects using quantitative PCR (qPCR). Our results indicate that overproduction of proinflammatory cytokines in HIV(+) individuals lead to increased production of free radicals. This combined with the decreased expression of GSH synthesis enzymes leads to a depletion of free GSH and may lead in part to the loss of immune function observed in HIV patients.
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