A Sabbagh, D Courtin, J Milet, J D Massaro, E C Castelli, F Migot-Nabias, B Favier, N Rouas-Freiss, P Moreau, A Garcia, E A Donadi
Institut de Recherche pour le Développement, UMR 216 Mère et enfant face aux infections tropicales, Paris, France. audrey.sabbagh@ird.fr
Tissue antigens 2013 JulHost and Plasmodium interactions result in highly variable clinical phenotypes, partly explained by the nature and level of anti-malarial antibody response. Human leukocyte antigen (HLA)-G can create a tolerogenic environment, allowing parasites to escape from anti-malarial immunity. We performed a family-based association study encompassing 483 Sereer individuals (261 children and their parents), and reported two independent signals at the HLA-G 3' untranslated region associated with antibody response to specific Plasmodium falciparum blood stage antigens, previously associated with malaria protection: (i) +3010G together with +3142C with total IgG and IgG1 against GLURP and (ii) +3196G with IgG3 against MSP2. While these results require further investigation, they suggest for the first time a role of HLA-G in the regulation of humoral immune response in malaria. © 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
A Sabbagh, D Courtin, J Milet, J D Massaro, E C Castelli, F Migot-Nabias, B Favier, N Rouas-Freiss, P Moreau, A Garcia, E A Donadi. Association of HLA-G 3' untranslated region polymorphisms with antibody response against Plasmodium falciparum antigens: preliminary results. Tissue antigens. 2013 Jul;82(1):53-8
PMID: 23745572
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