Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2019 Jul 3:10:830.
doi: 10.3389/fphys.2019.00830. eCollection 2019.

Deciphering Biological Processes at the Tick-Host Interface Opens New Strategies for Treatment of Human Diseases

Affiliations
Review

Deciphering Biological Processes at the Tick-Host Interface Opens New Strategies for Treatment of Human Diseases

Iveta Štibrániová et al. Front Physiol. .

Abstract

Ticks are obligatory blood-feeding ectoparasites, causing blood loss and skin damage in their hosts. In addition, ticks also transmit a number of various pathogenic microorganisms that cause serious diseases in humans and animals. Ticks evolved a wide array of salivary bioactive compounds that, upon injection into the host skin, inhibit or modulate host reactions such as hemostasis, inflammation and wound healing. Modulation of the tick attachment site in the host skin involves mainly molecules which affect physiological processes orchestrated by cytokines, chemokines and growth factors. Suppressing host defense reactions is crucial for tick survival and reproduction. Furthermore, pharmacologically active compounds in tick saliva have a promising therapeutic potential for treatment of some human diseases connected with disorders in hemostasis and immune system. These disorders are often associated to alterations in signaling pathways and dysregulation or overexpression of specific cytokines which, in turn, affect mechanisms of angiogenesis, cell motility and cytoskeletal regulation. Moreover, tick salivary molecules were found to exert cytotoxic and cytolytic effects on various tumor cells and have anti-angiogenic properties. Elucidation of the mode of action of tick bioactive molecules on the regulation of cell processes in their mammalian hosts could provide new tools for understanding the complex changes leading to immune disorders and cancer. Tick bioactive molecules may also be exploited as new pharmacological inhibitors of the signaling pathways of cytokines and thus help alleviate patient discomfort and increase patient survival. We review the current knowledge about tick salivary peptides and proteins that have been identified and functionally characterized in in vitro and/or in vivo models and their therapeutic perspective.

Keywords: host defense; immunological disorders; immunomodulation; pharmacological molecules; tick saliva.

PubMed Disclaimer

Figures

FIGURE 1
FIGURE 1
Effects of selected tick salivary proteins on host immune cells and their potential therapeutic usage to treat immunological disorders. IRS-2, BmTI, and Sialostatin L modulate functions of enzymes released by immune cells, resulting in inhibition of their biological and pathological functions.

Similar articles

Cited by

References

    1. Abrahamson M., Alvarez-Fernandez M., Nathanson C. M. (2003). Cystatins. Biochem. Soc. Symp. 70 179–199. - PubMed
    1. Akagi E. M., de Sá Júnior P. L., Simons S. M., Bellini M. H., Barreto S. A., Chudzinski-Tavassi A. M. (2012). Pro-apoptotic effects of amblyomin-X in murine renal cell carcinoma “in vitro”. Biomed. Pharmacother. 66 64–69. 10.1016/j.biopha.2011.11.015 - DOI - PubMed
    1. Aleman M. M., Wolberg A. S. (2013). Tick spit shines a light on the initiation of coagulation. Circulation 128 203–205. 10.1161/circulationaha.113.003800 - DOI - PMC - PubMed
    1. Anguita J., Ramamoorthi N., Hovius J. W. R., Das S., Thomas V., Persinski R., et al. (2002). Salp15, an Ixodes scapularis salivary protein, inhibits CD4+ T cell activation. Immunity 16 849–859. 10.1016/S1074-7613(02)00325-324 - DOI - PubMed
    1. Anisuzzaman, Alim M. A., Tsuji N. (2015). Longistatin in tick-saliva targets RAGE. Oncotarget 6 35133–35134. 10.18632/oncotarget.6032 - DOI - PMC - PubMed

LinkOut - more resources