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Principal Investigator: Jonathan Lawton
Organization: UNIVERSITY OF MARYLAND BALTIMORE
Fiscal Year: 2023
Award: $34,179
Funding agency: National Institute of Allergy and Infectious Diseases
PROJECT SUMMARY
Despite decades of research, Plasmodium falciparum malaria continues to kill hundreds of thousands of children
in sub-Saharan Africa each year. Vulnerability to severe malaria is complex, involving both host and parasite
factors. Blood type A is an established risk factor for severe malaria, whereas blood type O is associated with
protection from complicated symptoms. The exact mechanism of this phenomenon is incompletely understood
but may involve interactions mediated by particular parasite antigens. RIFINs and STEVORs are highly diverse
parasite protein families that are displayed on the surface of infected red blood cells. Recent laboratory studies
suggest that these antigens may exacerbate malaria severity through multiple mechanisms, including adherence
to nearby red blood cells to form “rosettes” that envelop the parasite and protect it from immune clearance.
Certain RIFINs bind preferentially to type A red blood cells. STEVORs have a similar binding preference for
glycophorin C, another red blood cell surface protein. These intriguing findings suggest that RIFINs and
STEVORs may be central to P. falciparum virulence and drive differences in susceptibility to severe disease
between blood types. Despite promising in vitro links to severe malaria vulnerability, the immense
diversity of the RIFIN and STEVOR families has so far precluded the comprehensive study of these
antigens in clinical infections. The goal of this proposal is to identify RIFIN and STEVOR subtypes that are
associated with severe malaria in African children. We will obtain blood and serum samples from children with
severe or non-severe malaria in Mali, Malawi, and Uganda, representing three regions of sub-Saharan Africa
with distinct malaria transmission patterns. In Aim 1, we will identify the expressed rif and stevor transcripts in
individual blood samples using reference-free RNA-Seq, then compare the abundance of transcript subgroups
between severe and non-severe malaria. In Aim 2, we will profile antibody responses against a comprehensive
microarray of RIFIN and STEVOR variants to identify immune “gaps” in children with severe malaria compared
to non-severe malaria. RIFIN and STEVOR antigen subtypes that were preferentially expressed and/or not
serorecognized in severe malaria infections may be important mediators of pathogenesis. RIFINs that
predominate in severe cases with blood type A may be critical aspects of this group’s vulnerability. The proposed
aims will help clarify the role of RIFINs and STEVORs in severe malaria pathogenesis and inform the
development of tailored vaccines and therapeutics to protect the most at-risk children in sub-Saharan Africa. The
applicant will develop and apply hands-on skills in transcriptomics, immunoepidemiology, and international
clinical research design and management, critical to his intended career as a 21st century molecular
epidemiologist.
Terms: <0-11 years old><Acute><Adherence><Africa South of the Sahara><African><Age><Amino Acid Sequence><Antibodies><Antibody Response><Antigens><Binding><Blood><Blood Grouping><Blood Reticuloendothelial System><Blood Sample><Blood Serum><Blood Typing><Blood erythrocyte><Blood specimen><Blood typing procedure><Cell Body><Cell Surface Antigens><Cell Surface Proteins><Cells><Cerebral Malaria><Child><Child Youth><Children (0-21)><Clinical><Clinical Research><Clinical Study><Complex><Convalescence><Custom><Development><Disease><Disorder><Epidemiologist><Erythrocyte Cytoskeleton><Erythrocyte Membrane><Erythrocytes><Erythrocytic><Falciparum Malaria><Family><Gene Expression><Generations><Genetic Polymorphism><Genome><Geographic Area><Geographic Locations><Geographic Region><Geographical Location><Glycophorin C><Goals><Human><Immune><Immunes><Immunity><Immunologic Epidemiology><Immunologic Surface Markers><Immunological Surface Markers><In Vitro><Individual><Infection><International><Invaded><Investigation><Laboratory Study><Length><Link><Malaria><Malawi><Mali><Marrow erythrocyte><Measures><Mediating><Mediator><Membrane Protein Gene><Membrane Proteins><Membrane-Associated Proteins><Messenger RNA><Modern Man><Molecular><Molecular Interaction><Morbidity><Morbidity - disease rate><Non-Polyadenylated RNA><Nyasaland><ORFs><Open Reading Frames><P falciparum><P. falciparum><P.falciparum><Paludism><Parasites><Pathogenesis><Pattern><Plasmodium Infections><Plasmodium falciparum><Plasmodium falciparum Malaria><Predisposition><Preparation><Primary Protein Structure><Protein Biochips><Protein Chips><Protein Coding Region><Protein Family><Protein Microarray><Protein Microchips><Proteins><RNA><RNA Gene Products><RNA Seq><RNA sequencing><RNAseq><Red Blood Cells><Red Cell><Research><Research Design><Ribonucleic Acid><Risk><Risk Factors><Role><Sampling><Serology><Serum><Severities><Site><Study Type><Sub-Saharan Africa><Subgroup><Subsaharan Africa><Surface><Surface Antigens><Surface Proteins><Susceptibility><Symptoms><Syndrome><Therapeutic><Time><Training><Transcript><Uganda><Vaccines><Variant><Variation><Virulence><Vulnerable Populations><ages><blood corpuscles><blood group><career><customs><design><designing><develop a vaccine><develop vaccines><development of a vaccine><developmental><disease phenotype><geographic site><immune clearance><immune elimination><immunoepidemiology><immunogen><kids><mRNA><malaria infection><malaria transmission><malaria-infected><malarial anemia><malarial infection><mortality><new approaches><next generation><novel approaches><novel strategies><novel strategy><polymorphism><preference><preparations><protein sequence><reference assembly><reference genome><response><skills><social role><study design><transcriptome sequencing><transcriptomic sequencing><transcriptomics><vaccine development><vulnerable group><vulnerable individual><vulnerable people><youngster>