Coxsackievirus 83 Vaccine
AssigneeKing Faisal University
InventorsJAWHAR GHARBI, MOHAMMED A. ALMALKI, AMEERA ALYAMI, MANEL BEN M'HADHEB
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Abstract
The Coxsackievirus B3 (CVB3) vaccine including a mutant strain of Coxsackievirus B3 (CVB3) (SEQ ID NO: 1) has specific double mutations introduced in the Internal Ribosome Entry Segment (IRES) region of the wild type Coxsackievirus B3 (CVB3) genome in the nucleotide positions 473 (in which uracil is substituted for cytosine) and 475 (in which cytosine is substituted for uracil). The resulting double mutant (SEQ ID NO: 1) demonstrates a significant decrease in its replicative capacity and a drastic decrease in its translation efficiency compared to the wild-type Coxsackievirus B3 (CVB3) strain.
Claims10
A composition, comprising:
- a live, attenuated double mutant strain of Coxsackievirus B3 comprising SEQ ID NO:
- 1, wherein cytosine is substituted by uracil at position nt. 473 and uracil is substituted by cytosine at position nt.475 in the genome of the wild type Coxsackievirus B3 in domain V within the internal ribosome entry segment (IRES), wherein
- the composition is formulated as a liquid suspension for oral administration, and
- the liquid suspension is provided within a capsule, the capsule being non-gastro-resistant.
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A method of vaccinating a subject against a Coksackievirus B3 (CVB3) strain infection, comprising administering to the subject vaccine against Coksackievirus B3 (CVB3) including a live, attenuated double mutant strain of Coxsackievirus B3 (SEQ ID NO:
- 1), wherein cytosine is substituted by uracil at position nt. 473 and uracil is substituted by cytosine at position nt.475 in the genome of the wild type Coxsackievirus B3 in domain V within the internal ribosome entry segment (IRES).
Dependencies are inferred from the claim text.