Immune Signature Against Antigens Predicts Clinical Immunity in Distinct Malaria Endemic Communities.

Mol Cell Proteomics

Centre for Molecular Therapeutics, Australian Institute of Tropical Health and Medicine, James Cook University, Cairns, QLD, Australia; QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia. Electronic address:

Published: January 2020

AI Article Synopsis

  • A significant amount of evidence shows that antibodies against malaria parasites help in developing natural immunity, but a specific antigen signature for predicting this immunity hasn't been found yet.
  • This research used samples from young children in Ghana to create a predictive model that identifies a signature of clinical immunity to malaria by analyzing antibody responses to just 15 target antigens.
  • The findings suggest that this immune signature can reliably predict clinical protection across different populations, potentially leading to a new point-of-care test for malaria risk and informing vaccination strategies.

Article Abstract

A large body of evidence supports the role of antibodies directed against the parasite in the development of naturally acquired immunity to malaria, however an antigen signature capable of predicting protective immunity against remains to be identified. Key challenges for the identification of a predictive immune signature include the high dimensionality of data produced by high-throughput technologies and the limitation of standard statistical tests in accounting for synergetic interactions between immune responses to multiple targets. In this study, using samples collected from young children in Ghana at multiple time points during a longitudinal study, we adapted a predictive modeling framework which combines feature selection and machine learning techniques to identify an antigen signature of clinical immunity to malaria. Our results show that an individual's immune status can be accurately predicted by measuring antibody responses to a small defined set of 15 target antigens. We further demonstrate that the identified immune signature is highly versatile and capable of providing precise and accurate estimates of clinical protection from malaria in an independent geographic community. Our findings pave the way for the development of a robust point-of-care test to identify individuals at high risk of disease and which could be applied to monitor the impact of vaccinations and other interventions. This approach could be also translated to biomarker discovery for other infectious diseases.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6944240PMC
http://dx.doi.org/10.1074/mcp.RA118.001256DOI Listing

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