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Last Updated: April 19, 2024

Claims for Patent: 5,853,735


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Summary for Patent: 5,853,735
Title: Avirulent anti-rabies vaccine
Abstract:The invention relates to an avirulent anti-rabies vaccine which consists of an avirulent mutant of an SAD strain of the rabies virus, the glycoprotein of which possesses in position 333 a naturally occurring amino acid whose codon differs from those of arginine by at least two nucleotides.
Inventor(s): Benejean; Jacqueline (Chilly Mazarin, FR), Flamand; Anne (Gif Sur Yvette, FR), Tuffereau; Marie-Christine (Paris, FR), Coulon; Patrice (Palaiseau, FR), Lafay; Florence (Versailles, FR)
Assignee: Virbac (FR)
Application Number:08/785,616
Patent Claims:1. An isolated double avirulent mutant of the SAD Berne strain of rabies virus, deposited in the Collection Nationale de Cultures de Micro-organismes (C.N.C.M.)-INSTITUT PASTEUR-FRANCE on 9th Jul. 1992 under no. I-1238, said mutant having in position 333 glutamic acid, whose codon differs from all codons of arginine by at least two nucleotides.

2. A method of obtaining the double base mutants according to claim 1, which comprises the steps of:

a) contacting a SAD strain of rabies virus with a first monoclonal antibody which neutralizes said SAD strain but does not neutralize the TAG1 strain of rabies virus, which TAG1 strain is deposited under n.degree.-I-433 in Collection Nationale de Cultures de Microorganismes;

b) selecting from said SAD strain of rabies virus, those mutants not neutralized by said first monoclonal antibody;

c) nucleotide-sequencing amino acid position 333 of the glycoprotein of said SAD mutants selected in step b;

d) isolating, from said SAD mutants nucleotide-sequenced in step c, those SAD mutants which possess a lysine in position 333;

e) preparing a second monoclonal antibody which neutralizes both the SAD strain and SAD mutants isolated in step b, but does not neutralize the said TAG1 strain; and

f) selecting from said SAD mutants selected in step b, those mutants which are not neutralized by said second monoclonal antibody.

3. An isolated avirulent anti-rabies vaccine which consists of an avirulent double base mutant of a SAD strain of the rabies virus, the glycoprotein of which possesses in position 333 a naturally occurring amino acid whose codon differs from all codons of arginine by at least two nucleotides; wherein said avirulent double base mutant is obtained from the process comprising the steps of:

a) contacting a SAD strain of rabies virus with a first monoclonal antibody which neutralizes said SAD strain but does not neutralize the TAG1 strain of rabies virus, which TAG1 strain is deposited under n.degree.-I-433 in Collection Nationale de Cultures de Microorganismes;

b) selecting from said SAD strain of rabies virus, those mutants not neutralized by said first monoclonal antibody;

c) nucleotide-sequencing amino acid position 333 of the glycoprotein of said SAD mutants selected in step b;

d) isolating, from said SAD mutants, nucleotide-sequenced in step c, those SAD mutants which possess a lysine in position 333;

e) preparing a second monoclonal antibody which neutralizes both the said SAD strain and mutants isolated in step d, but does not neutralize the said TAG1 strain; and

f) selecting from said SAD mutants selected in step b, those mutants which are not neutralized by said second monoclonal antibody.

4. A vaccine according to claim 3 wherein the amino acid in position 333 is glutamic acid.

5. A method of obtaining an isolated double base mutant avirulent anti-rabies vaccine possessing in position 333 an amino acid whose codon differs from all codons of arginine by at least two nucleotides, which comprises the steps of:

a) contacting a SAD strain of rabies virus with a first monoclonal antibody which neutralizes said SAD strain but does not neutralize the TAG1 strain of rabies virus, which TAG1 strain is deposited under n.degree.-I-433 in Collection Nationale de Cultures de Microorganismes;

b) selecting from said SAD strain of rabies virus, those mutants not neutralized by said first monoclonal antibody;

c) nucleotide-sequencing amino acid position 333 of the glycoprotein of said SAD mutants selected in step b;

d) isolating, from said SAD mutants nucleotide-sequenced in step c, those SAD mutants which possess a lysine in position 333;

e) preparing a second monoclonal antibody which neutralizes both the SAD strain and SAD mutants isolated in step d, but does not neutralize the said TAG1 strain; and

f) selecting from said SAD mutants selected in step b, those mutants which are not neutralized by said second monoclonal antibody.

6. A vaccine according to claim 3, wherein the mutant is a mutant of the SAD Berne strain.

7. A vaccine according to claim 6, wherein the mutant is the mutant deposited in the Collection Nationale de Cultures de Microorganismes C.N.C.M.-Institut PASTEUR-France, on 9th July 1992 under n.degree. I-1238, said mutant having in position 333 glutamic acid, whose codon differs from all codons of arginine by at least two nucleotides.

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