4.5 Article

How to get away with murder: The multiple strategies employed by pathogenic protozoa to avoid complement killing

Journal

MOLECULAR IMMUNOLOGY
Volume 149, Issue -, Pages 27-38

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.molimm.2022.05.118

Keywords

Complement system; Parasitic protozoa; Protozoal infection; Immune evasion; Complement regulation

Funding

  1. Coordenacao de Aperfeicoamento de NivelSuperior (CAPES)
  2. Fundacao a de Amparo a Pesquisa de Minas Gerais (FAPEMIG)

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Parasitic protozoa cause diseases with significant public health impact by evading the host immune system through various strategies. The complement system, an important effector mechanism, can lead to the elimination of parasites. Parasitic protozoa employ different strategies to avoid complement activation, including regulation and expression of complement system proteins, proteolytic cleavage of complement molecules, formation of physical barriers, and removal of bound complement molecules. This review summarizes the strategies used by parasitic protozoa to block complement activation and discusses new perspectives in this field.
Parasitic protozoa are eukaryotic unicellular organisms that depend on a variety of living organisms and can develop intra- and extracellularly inside their hosts. In humans, these parasites cause diseases with a significant impact on public health, such as malaria, toxoplasmosis, Chagas disease, leishmaniasis and amebiasis. The ability of a parasite in establishing a successful infection depends on a series of intricate evolutionarily selected adaptations, which include the development of molecular and cellular strategies to evade the host immune system effector mechanisms. The complement system is one of the main effector mechanisms and the first humoral shield of hosts innate immunity against pathogens. For unicellular pathogens, such as protozoa, bacteria and fungi, the activation of the complement system may culminate in the elimination of the invader mainly via 1- the formation of a pore that depolarizes the plasma membrane of the parasite, causing cell lysis; 2- opsonization and killing by phagocytes; 3- increasing vascular permeability while also recruiting neutrophils to the site of activation. Numerous strategies to avoid complement activation have been reported for parasitic protozoa, such as 1sequestration of complement system regulatory proteins produced by the host, 2- expression of complement system regulatory proteins, 3- proteolytic cleavage of different complement effector molecules, 4- formation of a physical glycolipid barrier that prevents deposition of complement molecules on the plasma membrane, and 5removal, by endocytosis, of complement molecules bound to plasma membrane. In this review, we revisit the different strategies of blocking various stages of complement activation described for the main species of parasitic protozoa, present the most recent discoveries in the field and discuss new perspectives on yet neglected strategies and possible new evasion mechanisms.

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