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Published on: August 6, 2020
Atypical memory B cell frequency correlates with antibody breadth and function in malaria immune adults
Frederica Dedo Partey1, Jasmine Naa Norkor Dowuona2, Abigail Naa Adjorkor Pobee2
1Noguchi Memorial Institute for Medical Research, University of Ghana, Legon, Ghana. fpartey@noguchi.ug.edu.gh.
Repeated malaria infections increase antibody breadth but lower antibody avidity. Atypical memory B cells correlate with broader antibody responses, suggesting a trade-off in malaria immunity.
Area of Science:
- Immunology
- Infectious Diseases
- Malariology
Background:
- Clinical immunity to malaria develops slowly and relies on antibodies.
- Chronic malaria exposure can disrupt B-cell homeostasis, leading to atypical memory B cells.
Purpose of the Study:
- To investigate how B-cell perturbations affect antibody breadth, avidity, and function in individuals with natural malaria exposure.
- To understand the impact of malaria transmission intensity on immune responses.
Main Methods:
- Comparing antibody profiles and B-cell subsets in individuals from high and low malaria transmission regions in Ghana.
- Assessing Plasmodium falciparum merozoite antigen-specific antibodies, antibody breadth, and avidity.
- Evaluating in vitro growth inhibition assays and their correlation with antibody characteristics.
Main Results:
- Individuals in high transmission areas had higher antigen-specific antibodies and broader antibody scores but lower avidity.
- Atypical memory B cell frequency was positively associated with antibody breadth.
- In vitro growth inhibition was linked to antibody reactivity breadth, not merozoite binding.
Conclusions:
- Repeated malaria infections impair high-avidity antibody development, compensated by increased antibody breadth.
- High malaria prevalence drives broader antibody diversity and maintains atypical memory B cell populations.
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