Development of low cost oral inactivated vaccines for dysentery

March.25.2016RESEARCH HIGHLIGHTS

Source: Okayama University (JAPAN), Public Relations and Information Strategy
For immediate release: 25 March 2016
Okayama University research: Development of low cost oral inactivated vaccines for dysentery

(Okayama, 25 March 2016) Okayama University researchers in collaboration with colleagues in India have developed inactivated vaccines a promising candidate for the production and commercialization of a low cost oral dysentery vaccine for use in developing countries.

Shin-ichi Miyoshi at the Okayama University Graduate School of Medicine and Dentistry and colleagues orally administration of a mixture of the six major Shigella serotypes of heat-killed bacteria sample preparations to laboratory animals in order to study the possibility of developing inactivated vaccines. The researchers conducted experiments using both passive and active immunization experimental systems and observed protective effect against infections with sufficient immunity-inducing effect (Figure 1 and 2).

Furthermore, in the tests using human cultured cells, the researchers did not find toxicity to the cells and observed strong production inducing immunity factors such as cytokines. This sample preparation has proved to be a promising candidate for oral dysentery vaccine. These sample preparations have proved to a promising candidate for the production and commercialization of a low cost oral dysentery vaccine. In the future, using the rhesus monkeys (natural host of Shigella), the researchers plan to study the protective and immunity-inducing effects as well as conducting clinical studies in Kolkata, India.

Background and expected outcome Okayama University was selected by MEXT as the center for emerging and re-emerging infectious diseases research base formation program and in 2007 the university established the "Okayama University India Infection Joint Research Centre to contribute to the control of the many deaths due diarrhea (cholera, dysentery) in India. One of the research projects is on the development of inexpensive oral dysentery vaccine because of the lack of dysentery vaccines for practical use.

Dysentery destroys intestinal tissue because it is a diarrheal disease with severe bleeding with deaths in developing countries such as India, reaching 600 thousand people annually. For this reason, the World Health Organization has designated the development of dysentery vaccine to be one of the most urgent research areas. Today, drug resistant Shigella is spreading fast and its treatment and the control of dysentery is becoming increasingly difficult.The results of this research are expected to lead to the development and commercialization of low-cost dysentery vaccines before the control of dysentery becomes extremely difficult.

Acknowledgments
The present study is being funded by the Education, Culture, Sports, Science and Technology Ministry (MEXT) as part of the emerging and re-emerging infectious diseases research COE program (FY 2007-2009); infectious disease research international network promotion program (FY 2010-2014); and National Research and Development Agency for the research and development mechanism infection (FY 2015).

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Reference
Barman S, Koley H, Nag D, Shinoda S, Nair GB, Takeda Y. Passive immunity with multi-serotype heat-killed Shigellae in neonatal mice. Microbiology and Immunology, 58:463-466 (2014)
DOI. 10.1111/1348-0421.12164
http://www.ncbi.nlm.nih.gov/pubmed/24909404

Nag D, Sinha R, Mitra S, Barman S, Takeda Y, Shinoda S, Chakrabarti MK, Koley H. Heat killed multi-serotype Shigella immunogens induced humoral immunity and protection against heterologous challenge in rabbit model. Immunobiology, 220:1275-1283 (2015)
DOI. 10.1016/j.imbio.2015.07.002
http://www.ncbi.nlm.nih.gov/pubmed/26210044

Correspondence to
Professor Shin-ichi Miyoshi, Ph.D.
Department of Environmental Health and Microbiology,
Graduate School of Medicine, Dentistry and Pharmaceutical
Sciences, Okayama University, 1-1-1 Tsushima-naka, Kita-ku,
Okayama 700-8530, Japan
E-mail: miyos-s(a)cc.okayama-u.ac.jp
For inquiries, please contact us by replacing (a) with the @ mark.

 

 

 


Figure 2. IgG secretion from peripheral blood mononuclear cells isolated from control or immunized rabbits.


Professor Shin-ichi Miyoshi


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