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Human vaccine against bird flu within reach after new discovery

Shiloh

Editor, Senior Moderator
Source: http://www.virtualmedicalcentre.com...d-flu-a-reality-with-new-discovery&odr=&page=

Human vaccine against bird flu a reality with new discovery
6 Apr 2009

A vaccine to protect humans from a bird flu pandemic is within reach after a new discovery by researchers at the University of Melbourne.

The discovery, published in the prestigious Proceedings of the National Academy of Science, reveals how boosting T cell immunity could better protect humans from a bird flu pandemic.


The continued spread of the highly virulent "bird flu" virus has experts worried that we are facing a new potential influenza pandemic which could transfer between humans. Furthermore, given the bird flu is new, there is no pre-existing immunity in the population and current vaccine formulations would be useless.

"The 'Killer T cell' is the hit-man of the immune system. It is able to locate and destroy virus-infected cells in our body helping rid us of infection," said A/Prof Stephen Turner, from the Department of Microbiology and Immunology at the University of Melbourne who is a lead author on the paper.

"Unfortunately, current influenza vaccines are poor at inducing killer T cell immunity. Therefore, we wanted to see if we could improve the current vaccine formulation to induce killer T cells after vaccination," he said.

"We added a compound, known to increase immunity, to the flu vaccine in an animal model. The addition of this compound promoted significant generation of potent killer T cell immunity and provided protection from infection.

"The significance of these findings is that rather than having to design a new vaccine altogether, we can improve current flu vaccines by adding this potent immune modulator.


"With appropriate clinical testing, we could see improvements to current vaccines within the next five years."


Dr Turner said the key to vaccine effectiveness was ensuring a match between the vaccine and the current circulating flu strain. However, the spike proteins varied over the course of a flu season rendering the current vaccine ineffective. As such, the vaccine needs to be updated every year to match the likely strain for that winter.

"It is a different situation for influenza pandemics. Pandemics arise due to the introduction of a new influenza virus into human circulation. As such, there is little or no pre-existing immunity to the bird flu virus enabling it to spread rapidly."

"'Killer' T cells recognise components that are conserved between different influenza viruses. Therefore, a vaccine strategy that induced killer T cells pre-emptively would provide protection from a potential pandemic."


(Source: University of Melbourne: Proceedings of the National Academy of Science: April 2009)
 
Re: Human vaccine against bird flu within reach after new discovery

Does anyone have access to the full paper? If so do they give further information on what they are adding to produce these effects. I would place strong bets that this will be a zinc based compound they are talking about.
 
Re: Human vaccine against bird flu within reach after new discovery

TNF/iNOS-producing dendritic cells are the necessary evil of lethal influenza virus infection

Jerry R. Aldridge, Jr.a, Carson E. Moseleya, David A. Boltza, Nicholas J. Negoveticha, Cory Reynoldsb, John Franksa, Scott A. Brownb, Peter C. Dohertyb, Robert G. Webstera,1 and Paul G. Thomasb
+Author Affiliations

aDivision of Virology, Department of Infectious Diseases, and
bDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105
Contributed by Robert G. Webster, January 20, 2009 (received for review December 23, 2008)

Abstract

Respiratory infection with highly pathogenic influenza A viruses is characterized by the exuberant production of cytokines and chemokines and the enhanced recruitment of innate inflammatory cells. Here, we show that challenging mice with virulent influenza A viruses, including currently circulating H5N1 strains, causes the increased selective accumulation of a particular dendritic cell subset, the tipDCs, in the pneumonic airways. These tipDCs are required for the further proliferation of influenza-specific CD8+ T cells in the infected lung, because blocking their recruitment in CCR2−/− mice decreases the numbers of CD8+ effectors and ultimately compromises virus clearance. However, diminution rather than total elimination of tipDC trafficking by treatment with the peroxisome proliferator-activated receptor-γ agonist pioglitazone moderates the potentially lethal consequences of excessive tipDC recruitment without abrogating CD8+ T cell expansion or compromising virus control. Targeting the tipDCs in this way thus offers possibilities for therapeutic intervention in the face of a catastrophic pandemic.

http://www.pnas.org/content/106/13/5306
 
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