CD68 acts as a major gateway for malaria sporozoite liver infection

Author:

Cha Sung-Jae11,Park Kiwon11,Srinivasan Prakash2,Schindler Christian W.33,van Rooijen Nico4,Stins Monique1,Jacobs-Lorena Marcelo11

Affiliation:

1. W. Harry Feinstone Department of Molecular Microbiology and Immunology and Johns Hopkins Malaria Research Institute, Bloomberg School of Public Health; and Department of Neurology, Johns Hopkins School of Medicine, Johns Hopkins University, Baltimore, MD 21205

2. Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD 20852

3. Department of Microbiology and Immunology and Department of Medicine, Columbia University, New York, NY 10032

4. Department of Molecular Cell Biology and Immunology, VUmc, 1081 BT Amsterdam, Netherlands

Abstract

After being delivered by the bite from an infected mosquito, Plasmodium sporozoites enter the blood circulation and infect the liver. Previous evidence suggests that Kupffer cells, a macrophage-like component of the liver blood vessel lining, are traversed by sporozoites to initiate liver invasion. However, the molecular determinants of sporozoite–Kupffer cell interactions are unknown. Understanding the molecular basis for this specific recognition may lead to novel therapeutic strategies to control malaria. Using a phage display library screen, we identified a peptide, P39, that strongly binds to the Kupffer cell surface and, importantly, inhibits sporozoite Kupffer cell entry. Furthermore, we determined that P39 binds to CD68, a putative receptor for sporozoite invasion of Kupffer cells that acts as a gateway for malaria infection of the liver.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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