• About napwha
  • About this site
  • Contact Us
  • Subscribe
  • napwha website
HIV Cure

Find out about current studies

Get Involved
  • Home
  • Science
    • Reservoir, Remission, Rebound
    • Latency Reversing Agents
    • Gene Therapy
    • Vaccines
    • Novel Approaches
    • Research Spotlight
  • Clinical Trials
    • Get Involved
  • Community
  • Media
  • Video

RV144 paving the way for future treatments

3 years ago NAPWHA Vaccines
Share this:

A new scientific study conducted by a team of leading AIDS scientists reveal results that lead the way to the development of an effective human vaccine against human immunodeficiency virus (HIV). In the study published in Nature Medicine, researchers worked with a species of Old World monkeys, rhesus macaques to reproduce the trial results of RV144, the only HIV vaccine that has been tested and shown to reduce the rate of HIV acquisition in a phase III clinical trial.

Researchers were interested in not only recapitulating the findings from the RV144 trial, but also determining if replacing the alum adjuvant–a substance commonly found in non-living vaccines known to induce antibody-mediated immunity–with a different adjuvant, MF59 would decrease simian immunodeficiency virus (SIV) acquisition at an increased rate and yield a more efficacious vaccine. Although MF59 is known to help stimulate the human body’s immune response, the idea that it could lead to greater vaccine efficacy is a popular working theory shared by scientists worldwide.

Full article at EurekAlert!

Case Western Reserve University RV144 vaccine

Previous Post

Antibody injections could be stepping stone to HIV vaccine

Next Post

AIDS 2016: hopes high in search for vaccine

NAPWHA

NAPWHA

Founded in 1989, The National Association of People with HIV Australia (NAPWHA) is Australia’s peak non-government organisation representing community-based groups of people living with HIV (PLHIV).

How broadly neutralising antibodies...

1 year ago

Paris highlights

2 years ago

Seattle HIV conference showcases...

2 years ago

Reports of UK HIV...

2 years ago
  • RT @LTU_Sex_Health: Mark your calendars for this important community event @LTU_Sex_Health in collaboration with several organisations is h…
    March 1st, 2019
  • RT @pozmagazine: The Road Ahead for #HIV Cure Research https://t.co/awLonoKHFe
    March 1st, 2019
  • RT @LTU_Sex_Health: Mark your calendars for this important community event @LTU_Sex_Health in collaboration with several organisations is h…
    February 26th, 2019

New clue about HIV latency maintenance

Yale researchers have highlighted the role of APOBEC3A (A3A) in sustaining HIV latency. A3A is typically found in immune cells such as macrophages. The new study shows that A3A is also found in CD4 T cells. Detailed experiments in lab models of HIV latency show that A3A blocks HIV reactivation. A3A binds directly to HIV, then brings in other repressive proteins which alter the DNA structure. These epigenetic changes prevent HIV reactivation. If A3A is found to act in a similar way in HIV infected people, it could form a new target for reversing latency and progressing towards a cure.

What should a functional cure for HIV aim to do?

Combination strategy delays virus rebound in monkeys

New light on tricky HIV structure

Immune profiling tool to identify exhausted cells

  • 2019
  • 2018
  • 2017
  • 2016
  • 2015
  • 2014
  • 2012

Supported by


Supported by the National Institute Of Allergy And Infectious Diseases of the National Institutes of Health under Award Number U19AI096109. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

About NAPWHA

Founded in 1989, The National Association of People with HIV Australia (NAPWHA) is Australia’s peak non-government organisation representing community-based groups of people living with HIV (PLHIV).
Copyright (c) 2019. National Association of people with HIV Australia. ABN: 79 052 437 899


To help us understand who is reading our site, please let us know why you’re here: