EBV Vaccine from QIMR Berghofer, Australia

If it's on your mind and it has to do with multiple sclerosis in any way, post it here.
Post Reply
User avatar
NHE
Volunteer Moderator
Posts: 6238
Joined: Sat Nov 20, 2004 3:00 pm
Contact:

EBV Vaccine from QIMR Berghofer, Australia

Post by NHE »

First-Ever Vaccine Candidate Against Epstein-Barr Delivers Promising Results

August 9, 2023 by David Nield

https://www.sciencealert.com/first-ever ... ng-results

Researchers have made a significant breakthrough in the development of the first-ever vaccine for the Epstein-Barr virus (EBV), a virus that causes infectious mononucleosis (IM, or 'mono') – also known as glandular fever.

The virus can infamously lead to further health issues like cancer and multiple sclerosis (MS).

The team of scientists, from the QIMR Berghofer Medical Research Institute in Australia, have been able to design a vaccine targeting lymph nodes in mice, which are key players in the functioning of the body's immune system.

Not only did the vaccine produce strong, long-lasting antibodies and T cells to fight EBV, it was also shown to induce a particular kind of immunity to protect against the growth of EBV-associated tumors. By blocking EBV activity early, the drug prevents secondary issues, like brain inflammation that can lead to MS.

Image

That combination of antibodies and T cells, which both play different but very important roles in the immune system, is crucial. Antibodies bind to unwanted, invading pathogens to eliminate them, while T cells directly destroy these pathogens and help coordinate the body's defenses.

"What we have done is we have designed what we call another arm of the immune system, that we call T cells, and combined that with antibody, and this new formulation will induce both – both the antibody and the T cell immune response," says Rajiv Khanna, an immunologist at the QIMR Berghofer Medical Research Institute.

"It is now very much well established that to give long-term protection against EBV-associated diseases, you don't only just need antibodies but also the T cell immunity."

EBV is a member of the herpes family of viruses and can be passed around through saliva. Although at least 95 percent of the world's population have the virus, for most of us that happens at a very early age, and doesn't lead to any serious symptoms. The virus is then carried harmlessly around with us for the rest of our lives.

Problems happen when someone doesn't get that early dose and is infected with EBV later on, especially in adolescence. That's when the effects of the virus can be much more severe, leading to mono (or glandular fever), and an increased risk of certain kinds of throat and nose cancers as well as multiple sclerosis.

Scientists are busy trying to limit the damage done by EBV in the body, and part of the challenge is figuring out how the virus manages to be so destructive for some people and barely noticeable for others.

When it comes to human clinical trials, the team already has some funding from industry partners, and is looking for more to make the trials as comprehensive as possible. Those trials could start in 2024 or 2025 if all goes well.

"It has been very satisfying," says Vijayendra Dasari, a vaccine development scientist from the QIMR Berghofer Medical Research Institute. "Now we are kind of getting close to the final stages of development."

The research has been published in Nature Communications.
User avatar
NHE
Volunteer Moderator
Posts: 6238
Joined: Sat Nov 20, 2004 3:00 pm
Contact:

Re: EBV Vaccine from QIMR Berghofer, Australia

Post by NHE »

Lymph node targeted multi-epitope subunit vaccine promotes effective immunity to EBV in HLA-expressing mice
Nat Commun. 2023 Aug 8;14(1):4371.

The recent emergence of a causal link between Epstein-Barr virus (EBV) and multiple sclerosis has generated considerable interest in the development of an effective vaccine against EBV. Here we describe a vaccine formulation based on a lymph node targeting Amphiphile vaccine adjuvant, Amphiphile-CpG, admixed with EBV gp350 glycoprotein and an engineered EBV polyepitope protein that includes 20 CD8+ T cell epitopes from EBV latent and lytic antigens. Potent gp350-specific IgG responses are induced in mice with titers >100,000 in Amphiphile-CpG vaccinated mice. Immunization including Amphiphile-CpG also induces high frequencies of polyfunctional gp350-specific CD4+ T cells and EBV-specific CD8+ T cells that are 2-fold greater than soluble CpG and are maintained for >7 months post immunization. This combination of broad humoral and cellular immunity against multiple viral determinants is likely to provide better protection against primary infection and control of latently infected B cells leading to protection against the development of EBV-associated diseases.

Free full text
Post Reply
  • Similar Topics
    Replies
    Views
    Last post

Return to “General Discussion”