Binding Molecules in Tick Saliva for Targeting Host Cytokines, Chemokines, and Beyond

Ticks have coevolved with their hosts over millions of years, developing the ability to evade hemostatic, inflammatory, and immunological responses. Salivary molecules from these vectors bind to cytokines, chemokines, antibodies, complement system proteins, vasodilators, and molecules involved in co...

Full description

Saved in:
Bibliographic Details
Published inBiomolecules (Basel, Switzerland) Vol. 14; no. 12; p. 1647
Main Authors Desidério, Chamberttan Souza, Flávio-Reis, Victor Hugo Palhares, Pessoa-Gonçalves, Yago Marcos, Tiveron, Rafael Destro Rosa, Sales-Campos, Helioswilton, Felice, Andrei Giacchetto, Soares, Siomar de Castro, Guillermo-Ferreira, Rhainer, Rodrigues, Wellington Francisco, Oliveira, Carlo José Freire
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 01.12.2024
MDPI
Subjects
Online AccessGet full text
ISSN2218-273X
2218-273X
DOI10.3390/biom14121647

Cover

More Information
Summary:Ticks have coevolved with their hosts over millions of years, developing the ability to evade hemostatic, inflammatory, and immunological responses. Salivary molecules from these vectors bind to cytokines, chemokines, antibodies, complement system proteins, vasodilators, and molecules involved in coagulation and platelet aggregation, among others, inhibiting or blocking their activities. Initially studied to understand the complexities of tick–host interactions, these molecules have been more recently recognized for their potential clinical applications. Their ability to bind to soluble molecules and modulate important physiological systems, such as immunity, hemostasis, and coagulation, positions them as promising candidates for future therapeutic development. This review aims to identify the binding molecules present in tick saliva, determine their primary targets, and explore the tick species involved in these processes. By associating the binding molecules, the molecules to which they bind, and the effect caused, the review provides a basis for understanding how these molecules can contribute to possible future advances in clinical applications.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ObjectType-Review-3
content type line 23
These authors contributed equally to this work.
ISSN:2218-273X
2218-273X
DOI:10.3390/biom14121647