Volume 9 Issue 116
Published - 14:00 UTC 08:00 EST 27-Apr-2007 
Next Update - 14:00 UTC 08:00 EST 28-Apr-2007

Editor: Susan K. Boyer, RN
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Oral vaccine containing salmonella may protect against aerosolized anthrax

(27 April 2007: VIDYYA MEDICAL NEWS SERVICE) -- Researchers from the U.S. and abroad have developed an orally administered Salmonella-based vaccine that protects mice against aerosolized anthrax and may also have human implications. They report their findings in the April 2007 issue of the journal Infection and Immunity.

Anthrax is a deadly disease that affects wildlife, livestock and humans and presents a serious threat as a potential biological weapon. Currently, there is a vaccine licensed for use in the US and the United Kingdom, and although effective, it requires multiple injections over several months, is expensive to produce and is only available to military personnel. A safe, effective and long-lasting vaccine available to civilians is necessary to protect mass populations in the event of an attack.

In the study researchers produced Salmonella enterica serovar Typhimurium expressing differing levels of the necessary protective antigen to induce anthrax immunity and orally immunized groups of mice. Following immunization the mice were then challenged with aerosolized anthrax spores. Five of the six mice that received the vaccine containing full expression of the antigen were protected against infection, while the vaccine with reduced antigen levels only provided up to 25 % protection.

“In the present study, we have shown for the first time that orally administered Salmonella expressing PA is able to protect mice against infection caused by airborne B. anthracis,” say the researchers.

(M.G.M. Stokes, R.W. Titball, B.N. Neeson, J.E. Galen, N.J. Walker, A.J. Stagg, D.C. Jenner, J.E. Thwaite, J.P. Nataro, L.W.J. Baillie, H.S. Atkins. 2007. Oral administration of a Salmonella enterica-based vaccine expressing Bacillus anthracis protective antigen confers protection against aerosolized B. anthracis. Infection and Immunity, 75. 4: 1827-1834).

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