New ads.

Showing posts with label vaccine. Show all posts
Showing posts with label vaccine. Show all posts

Wednesday, January 8, 2020

Breakthrough in Zika virus vaccine

Illustration of Zika virus in blood (stock image).
Credit: © Kateryna_Kon / Adobe Stock

Researchers from the University of Adelaide have made significant advances in developing a novel vaccine against Zika virus, which could potentially lead to global elimination of the disease.
The virology team, led by Professor Eric Gowans and Dr Branka Grubor-Bauk -- based at the Basil Hetzel Institute for Translational Health Research and supported by The Hospital Research Foundation -- has developed a vaccine that prevents Zika infection in pre-clinical models of the disease.
Their findings have been published today in the leading international journal Science Advances.
Zika is a mosquito-transmitted 'flavivirus' which can cause microcephaly (a birth defect where a baby's head is significantly smaller than expected) and severe birth defects in infants born to infected mothers.
The introduction of an effective vaccine for Zika will prevent infection of pregnant women and the resultant congenital effects in the unborn child.
Dr Grubor-Bauk, senior research officer with the Adelaide Medical School, said the team had developed a novel vaccine against Zika that proved effective in mouse models.
"This is the first vaccine study that shows that a T cell-based vaccine can confer protection against a systemic Zika infection,'' she said.
"Our vaccine offers an advantage over other vaccines in development by eliminating the ongoing concerns in the field about enhancement of infection following exposure to dengue virus. This finding demonstrates for the first time that protective T cell vaccines against Zika are achievable.
"Zika virus is extremely detrimental if you're pregnant and there has been no therapy or vaccine available to date. If we can progress this work and immunise women who are of reproductive age and most at risk, we can stop the devastating effects of Zika infection in pregnancy and make a huge difference to the health of the global community."
This research, which has been years in the making, has progressed to this significant stage thanks to funding from National Foundation for Medical Research and Innovation (NFMRI) and ongoing funding from The Hospital Research Foundation.
The work was done in collaboration with eminent global vaccine researcher Prof Dan Barouch, Director of Harvard Medical School's Centre for Virology and Vaccine Research (CVVR) at Beth Israel Deaconess Medical Centre; as well as Adelaide's Prof Sarah Robertson, Director of the Robinson Research Institute, University of Adelaide; and other scientists from the universities of Adelaide, South Australia and Flinders.
"The next steps are to advance the vaccine to being ready for Phase I human clinical trials. This involves further pre-clinical studies which are vitally important to identify the most effective dosing and demonstrate protection against Zika infection in different pre-clinical models of the disease," Dr Grubor-Bauk said.
"The goal is to de-risk and create an attractive technology with a strong IP position, for licensing or co-development with a commercial partner.
"We are grateful to The Hospital Research Foundation which has been instrumental in their support of our research over this time. We could not have reached this point without them."
The findings of this study will also greatly inform other research in the development of flavivirus vaccines by shifting the focus of vaccine development from viral envelope and antibody-based vaccines to T-cell based vaccines.

Story Source:
Materials provided by University of Adelaide. Original written by Elisa Black. Note: Content may be edited for style and length.

Monday, December 23, 2019

Breakthrough in Zika virus vaccine

Illustration of Zika virus in blood (stock image).

Researchers from the University of Adelaide have made significant advances in developing a novel vaccine against Zika virus, which could potentially lead to global elimination of the disease.

The virology team, led by Professor Eric Gowans and Dr Branka Grubor-Bauk -- based at the Basil Hetzel Institute for Translational Health Research and supported by The Hospital Research Foundation -- has developed a vaccine that prevents Zika infection in pre-clinical models of the disease.
Their findings have been published today in the leading international journal Science Advances.
Zika is a mosquito-transmitted 'flavivirus' which can cause microcephaly (a birth defect where a baby's head is significantly smaller than expected) and severe birth defects in infants born to infected mothers.
The introduction of an effective vaccine for Zika will prevent infection of pregnant women and the resultant congenital effects in the unborn child.
Dr Grubor-Bauk, senior research officer with the Adelaide Medical School, said the team had developed a novel vaccine against Zika that proved effective in mouse models.
"This is the first vaccine study that shows that a T cell-based vaccine can confer protection against a systemic Zika infection,'' she said.
"Our vaccine offers an advantage over other vaccines in development by eliminating the ongoing concerns in the field about enhancement of infection following exposure to dengue virus. This finding demonstrates for the first time that protective T cell vaccines against Zika are achievable.
"Zika virus is extremely detrimental if you're pregnant and there has been no therapy or vaccine available to date. If we can progress this work and immunise women who are of reproductive age and most at risk, we can stop the devastating effects of Zika infection in pregnancy and make a huge difference to the health of the global community."
This research, which has been years in the making, has progressed to this significant stage thanks to funding from National Foundation for Medical Research and Innovation (NFMRI) and ongoing funding from The Hospital Research Foundation.
The work was done in collaboration with eminent global vaccine researcher Prof Dan Barouch, Director of Harvard Medical School's Centre for Virology and Vaccine Research (CVVR) at Beth Israel Deaconess Medical Centre; as well as Adelaide's Prof Sarah Robertson, Director of the Robinson Research Institute, University of Adelaide; and other scientists from the universities of Adelaide, South Australia and Flinders.
"The next steps are to advance the vaccine to being ready for Phase I human clinical trials. This involves further pre-clinical studies which are vitally important to identify the most effective dosing and demonstrate protection against Zika infection in different pre-clinical models of the disease," Dr Grubor-Bauk said.
"The goal is to de-risk and create an attractive technology with a strong IP position, for licensing or co-development with a commercial partner.
"We are grateful to The Hospital Research Foundation which has been instrumental in their support of our research over this time. We could not have reached this point without them."
The findings of this study will also greatly inform other research in the development of flavivirus vaccines by shifting the focus of vaccine development from viral envelope and antibody-based vaccines to T-cell based vaccines.

Thursday, November 14, 2019

New findings could lead to improved vaccinations against sexually transmitted infections

In a study published today in the Nature Communications, researchers from King's College London have shown how skin vaccination can generate protective CD8 T-cells that are recruited to the genital tissues and could be used as a vaccination strategy for sexually transmitted infections (STIs).
One of the challenges in developing vaccines for STIs, such as HIV or herpes simplex virus, is understanding how to attract specialised immune cells, called CD8 T-cells, to take up residence in the part of the body where the virus first enters. These cells need to be in place, armed and ready to provide an immediate protective immune defence, rather than waiting for immune cells in the blood to enter the tissues which takes time.
Before this study, it was thought that vaccines ideally needed to be delivered directly to the body surface (e.g. female genital tissue) where the infection might start, so that the immune system can generate these CD8 T-cells, travel back to the vaccination site and eliminate any future virus that is encountered. However, delivering vaccines directly to the female genital tissue is neither patient friendly nor efficient.
Now the team from King's have found that their vaccination strategy marshals a platoon of immune cells, called innate lymphoid cells (ILC1) and monocytes, in the genital tissues to work together and release chemicals (chemokines) to send out a call to the CD8 T-cells generated by the vaccine to troop into the genital tissue.
This research builds on the team's earlier work to develop skin vaccination techniques using a dissolvable 'microneedle' vaccine patch that once placed against the skin dissolves and releases the vaccine without requiring a hypodermic needle injection and generates immune responses.
Lead author, Professor Linda Klavinskis from King's College London said: "This study highlights how specialised groups of 'innate' immune cells in distant tissues can be harnessed to attract protective CD8 T-cells, arming the body's frontline tissues from infection.
"We now need to confirm these results with other types of vaccines from the one used in the study to see if a common pathway is triggered by skin vaccination. If proven, this could have a significant impact in improving the effectiveness of vaccines against sexually transmitted infections."