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Author Notes:

William Yavo.

yavowilliam@yahoo.fr.

MA wrote the first draft of the review. The other authors (AO, DO, S-PN, and WY) read and made revisions to the first draft and approved the final version for publication. All authors contributed to the article and approved the submitted version.

We thank Professor A. Djimde for supporting this research and the Database of Single Nucleotide Polymorphisms (dbSNP) for kindly allowing the use of their database resources in this review.

The authors declare that this research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Subjects:

Research Funding:

This work was supported by the Developing Excellence in Leadership and Genetics Training for Malaria Elimination (DELGEME) program in sub-Saharan Africa (Grant number: PD00217ML) through the DELTAS Africa Initiative (Grant number: 107740/Z/15/Z). The DELTAS Africa Initiative is an independent funding scheme of the African Academy of Sciences (AAS)’s Alliance for Accelerating Excellence in Science in Africa (AESA) and is supported by the New Partnership for Africa’s Development Planning and Coordinating Agency (NEPAD Agency) with funding from the Wellcome Trust (Grant number: PD00217ML) and the United Kingdom government.

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Immunology
  • Fc gamma receptors
  • polymorphism
  • malaria
  • immunoglobulin G
  • susceptibility
  • SYSTEMIC-LUPUS-ERYTHEMATOSUS
  • SINGLE-NUCLEOTIDE POLYMORPHISMS
  • AFFINITY IGG RECEPTOR
  • IIA CD32 POLYMORPHISM
  • NATURAL-KILLER-CELLS
  • IMMUNOGLOBULIN-G
  • SIGNAL-TRANSDUCTION
  • IIIB POLYMORPHISMS
  • 3 GENES
  • ASSOCIATION

Polymorphisms in Fc Gamma Receptors and Susceptibility to Malaria in an Endemic Population

Tools:

Journal Title:

FRONTIERS IN IMMUNOLOGY

Volume:

Volume 11

Publisher:

, Pages 561142-561142

Type of Work:

Article | Final Publisher PDF

Abstract:

Repeated infections by Plasmodium falciparum result in a humoral response that could reduce disease symptoms and prevent the development of clinical malaria. The principal mechanism underlying this humoral response is that immunoglobulin G (IgG) binds directly to the parasites, thus causing their neutralization. However, the action of antibodies alone is not always sufficient to eliminate pathogens from an organism. One key element involved in the recognition of IgG that plays a crucial role in the destruction of the parasites responsible for spreading malaria is the family of Fc gamma receptors. These receptors are expressed on the surface of immune cells. Several polymorphisms have been detected in the genes encoding these receptors, associated with susceptibility or resistance to malaria in different populations. In this review, we describe identified polymorphisms within the family of Fc gamma receptors and the impact of these variations on the response of a host to infection as well as provide new perspectives for the design of an effective vaccine for malaria.

Copyright information:

© 2020 Amiah, Ouattara, Okou, N’Guetta and Yavo.

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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