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Tick immunity using mRNA, DNA and protein-based Salp14 delivery strategies
Jaqueline Matias1, Cheyne Kurokawa1, Andaleeb Sajid1
1Section of Infectious Diseases, Yale University School of Medicine, New Haven, CT 06520, USA.
Vaccine
|December 4, 2021
Summary
Guinea pigs develop tick immunity against Ixodes scapularis. mRNA lipid nanoparticles (LNPs) delivering Salp14 antigen show promise for enhancing tick resistance and preventing tick-borne diseases.
Area of Science:
- Immunology
- Parasitology
- Vaccine Development
Background:
- Guinea pigs develop acquired resistance to Ixodes scapularis ticks, known as tick immunity.
- Tick immunity is influenced by salivary components, including the anticoagulant Salp14, which is associated with partial immunity.
Purpose of the Study:
- To investigate how different antigen delivery platforms (mRNA-LNPs, DNA, recombinant protein) influence the development of tick immunity using Salp14 as a model antigen.
- To evaluate the efficacy of mRNA-LNPs in eliciting early hallmarks of tick resistance.
Main Methods:
- Utilized Salp14 as a model antigen delivered via mRNA-lipid nanoparticles (LNPs), plasmid DNA, or recombinant protein.
- Assessed tick immunity by measuring erythema at the tick bite site and evaluating humoral and cellular responses post-tick challenge.
Main Results:
- mRNA-LNP vaccination elicited earlier and more pronounced erythema at the tick bite site compared to DNA or protein immunizations.
- Immune responses were directed towards a specific carboxy-terminal region of Salp14.
- mRNA-LNPs demonstrated potential in eliciting early indicators of acquired tick resistance.
Conclusions:
- The vaccine platform significantly influences the development of tick immunity in guinea pigs.
- mRNA-LNPs represent a promising platform for developing vaccines against tick-borne diseases by enhancing tick resistance mechanisms.

