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Author Notes:

Mary R. Galinski, Email: mary.galinkski@emory.edu

MRG developed the content and wrote the manuscript. The author read and approved the final manuscript.

Special thanks are extended to Eberhard O. Voit for his critical reading of an initial draft of this paper, and providing editorial feedback and suggestions, and to Chester J. Joyner for contributing his ideas and ongoing insights and discussion relating to malaria, immunity, pathogenesis, and research using nonhuman primates. The MaHPIC team is also acknowledged for 10 years of dedication and discussion towards improved understanding of malaria using nonhuman primates and systems biological approaches.

The authors declare that they have no competing interests.

Subject:

Research Funding:

The MaHPIC work reviewed here was funded in part by the National Institute of Allergy and Infectious Diseases; National Institutes of Health, Department of Health and Human Services, which established the MaHPIC [Contract No. HHSN272201200031C; MG], the NIH Office of Research Infrastructure Programs/OD P51OD011132, the Defense Advanced Research Program Agency and the US Army Research Office via a cooperative agreement [Contract No. W911NF16C0008; MG], which funded the Technologies for Host Resilience-Host Acute Models of Malaria to study Experimental Resilience (THoR’s HAMMER) consortium. The funding bodies did not participate in the development of this article.

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Infectious Diseases
  • Parasitology
  • Tropical Medicine
  • Plasmodium
  • Host-pathogen interactions
  • Pathogenesis
  • Immunity
  • Systems immunology
  • Gametocytes
  • Rhesus macaques
  • Macaca mulatta
  • Macaca fascicularis
  • New World monkeys
  • PLASMODIUM-FALCIPARUM INFECTION
  • MEMORY B-CELLS
  • DUFFY-BLOOD-GROUP
  • SPOROZOITE CHALLENGE MODEL
  • DEEP VASCULAR SCHIZOGONY
  • ANTIGENIC VARIATION
  • VIVAX MALARIA
  • MACACA-MULATTA
  • ERYTHROCYTE INVASION
  • CYNOMOLGI INFECTIONS

Systems biology of malaria explored with nonhuman primates

Tools:

Journal Title:

MALARIA JOURNAL

Volume:

Volume 21, Number 1

Publisher:

, Pages 177-177

Type of Work:

Article | Final Publisher PDF

Abstract:

“The Primate Malarias” book has been a uniquely important resource for multiple generations of scientists, since its debut in 1971, and remains pertinent to the present day. Indeed, nonhuman primates (NHPs) have been instrumental for major breakthroughs in basic and pre-clinical research on malaria for over 50 years. Research involving NHPs have provided critical insights and data that have been essential for malaria research on many parasite species, drugs, vaccines, pathogenesis, and transmission, leading to improved clinical care and advancing research goals for malaria control, elimination, and eradication. Whilst most malaria scientists over the decades have been studying Plasmodium falciparum, with NHP infections, in clinical studies with humans, or using in vitro culture or rodent model systems, others have been dedicated to advancing research on Plasmodium vivax, as well as on phylogenetically related simian species, including Plasmodium cynomolgi, Plasmodium coatneyi, and Plasmodium knowlesi. In-depth study of these four phylogenetically related species over the years has spawned the design of NHP longitudinal infection strategies for gathering information about ongoing infections, which can be related to human infections. These Plasmodium-NHP infection model systems are reviewed here, with emphasis on modern systems biological approaches to studying longitudinal infections, pathogenesis, immunity, and vaccines. Recent discoveries capitalizing on NHP longitudinal infections include an advanced understanding of chronic infections, relapses, anaemia, and immune memory. With quickly emerging new technological advances, more in-depth research and mechanistic discoveries can be anticipated on these and additional critical topics, including hypnozoite biology, antigenic variation, gametocyte transmission, bone marrow dysfunction, and loss of uninfected RBCs. New strategies and insights published by the Malaria Host–Pathogen Interaction Center (MaHPIC) are recapped here along with a vision that stresses the importance of educating future experts well trained in utilizing NHP infection model systems for the pursuit of innovative, effective interventions against malaria.

Copyright information:

© The Author(s) 2022

This is an Open Access work distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/rdf).
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