Recombinant bacillus calmette-guerin vaccine secreting bacteria resuscitation somatomedin and application thereof
A technology of growth-promoting factor and recombinant BCG, which is applied in the field of medicine and biology, can solve the problems such as the ineffective effect of BCG, and achieve the effect of preventing activation and inhibiting proliferation
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Patents(China)
- Current Assignee / Owner
- Publication Date
- 2012-05-09
- Estimated Expiration
- Not applicable · inactive patent
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Abstract
Description
technical field
[0001] The invention belongs to the technical field of medicine and biology, and relates to a recombinant BCG vaccine, in particular to a recombinant BCG vaccine that secretes bacteria resuscitating growth-promoting factors and an application thereof. Background technique
[0002] 1. Recombinant BCG is an effective way to prepare TB vaccine
[0003] Bacillus Calmette-Guerin vaccine (BCG), an attenuated live Mycobacterium bovis, is currently the most effective vaccine against tuberculosis and has been vaccinated by 3.5 billion people worldwide since 1948. With the deepening of research, people found that BCG is not only a live vaccine, but also an expression carrier of foreign genes. This discovery opened up a new field for the application of BCG.
[0004] rBCG (Recombinate BCG) uses BCG as an engineering bacterium, uses genetic engineering technology to introduce several foreign genes into the same BCG, and relies on the long-term survival of BCG in the host...
Examples
Embodiment Construction
[0039] The invention provides a recombinant BCG vaccine that secretes bacterial resuscitation growth-promoting factor. On the basis of constructing exogenous expression vector pDE22-Rpf, it is transfected with BCG to prepare recombinant BCG vaccine, and rBCG-Rpf is obtained through resistance screening; and The expression of the target gene and the immune effect of rBCG-Rpf were verified. The present invention will be further described in detail below in conjunction with the accompanying drawings, which are explanations rather than limitations of the present invention.
[0041] The Rpf gene was cloned by PCR using M.luteus DNA as a template, and the amplification primer P was designed as follows:
[0042] Upstream primer P1: cga ggatcc a ccatggacac catgact 27;
[0043] Downstream primer P2: tca aagctt t caggcctgcg gcaggac 27;
[0044] The upstream primer P1 introduces a BamHI restriction site ggatcc , the downstream primer P2 introduces...