
Targets for developing recombinant protein based veterinary vaccines
- Dr. Lei Li
- Vaccine , Biotech
- May 27, 2025
Table of Contents
Developing recombinant protein-based vaccines for pets is a promising approach to reduce reactogenicity and side effects compared to traditional inactivated vaccines. Below are key diseases and strategic suggestions for our focus:
1. High-Priority Diseases with Existing Vaccine Limitations
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Feline Leukemia Virus (FeLV)
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Rationale: Current vaccines may have variable efficacy and occasional side effects.
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Target Antigen: Recombinant envelope protein (p45) or novel fusion proteins.
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Advantage: Improved safety and longer-lasting immunity for high-risk cats (outdoor/multi-cat households).
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Canine Lyme Disease (Borrelia burgdorferi)
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Rationale: Existing OspA-based vaccines may lack coverage against emerging strains.
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Target Antigen: Recombinant chimeric OspA/OspC proteins or conserved epitopes.
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Advantage: Broader protection and reduced risk of vaccine-associated arthritis.
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Leptospirosis
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Rationale: Inactivated vaccines target limited serovars and have short-lived immunity.
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Target Antigen: Recombinant conserved outer membrane proteins (e.g., LipL32) or multi-serovar cocktails.
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Advantage: Enhanced cross-protection and reduced hypersensitivity reactions.
2. Diseases with No/Underdeveloped Vaccines
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Feline Infectious Peritonitis (FIP)
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Rationale: No effective vaccine exists; high mortality in cats.
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Target Antigen: Recombinant spike (S) protein of feline coronavirus (mutated for immune evasion).
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Challenge: Balance immunity without triggering antibody-dependent enhancement (ADE).
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Canine Leishmaniasis
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Rationale: Existing vaccines have limited efficacy against this zoonotic protozoan disease.
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Target Antigen: Recombinant Leishmania antigens (e.g., gp63, LACK) to stimulate Th1 immunity.
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Advantage: Prophylactic and therapeutic potential in endemic regions.
3. Maternal Antibody Interference Challenges
- Canine Parvovirus (CPV) and Distemper
- Rationale: Live vaccines can be neutralized by maternal antibodies in puppies.
- Target Antigen: Recombinant VP2 (CPV) or F/H proteins (distemper) with adjuvants to bypass interference.
- Advantage: Enable earlier, safer vaccination in young animals.
4. Zoonotic and Emerging Pathogens
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Rabies
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Rationale: Inactivated vaccines are safe but may cause local reactions.
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Target Antigen: Recombinant glycoprotein G (as used in oral wildlife vaccines).
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Advantage: Safer booster vaccines for pets, especially in sensitive individuals.
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Canine Influenza (H3N8/H3N2)
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Rationale: Strain-specific vaccines limit coverage.
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Target Antigen: Recombinant hemagglutinin (HA) proteins from multiple strains.
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Advantage: Broad-spectrum protection against evolving strains.
5. Highly Variable or Underaddressed Pathogens
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Feline Calicivirus (FCV)
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Rationale: Current vaccines struggle with viral diversity.
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Target Antigen: Recombinant VP1 capsid proteins targeting conserved regions.
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Advantage: Cross-protection against multiple FCV strains.
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Giardiasis
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Rationale: Limited vaccine uptake due to modest efficacy.
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Target Antigen: Recombinant cyst wall proteins or variable surface proteins (VSPs).
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Advantage: Mucosal immunity to reduce shedding and zoonotic risk.
Strategic Considerations
- Adjuvant Selection: Pair antigens with novel adjuvants (e.g., TLR agonists) to enhance immune responses without inflammation.
- Combination Vaccines: Develop multi-antigen vaccines (e.g., Lyme + leptospirosis) to simplify pet healthcare.
- Market Focus: Prioritize diseases with high owner awareness (e.g., rabies, Lyme) or unmet needs (e.g., FIP, leishmaniasis).
- Regulatory Pathways: Collaborate with veterinary agencies to streamline approval for recombinant platforms.
By targeting these areas, the recombinant protein vaccines could address critical gaps in safety, efficacy, and coverage, offering a competitive edge in the pet vaccine market.