期刊名称:Proceedings of the National Academy of Sciences
印刷版ISSN:0027-8424
电子版ISSN:1091-6490
出版年度:2022
卷号:119
期号:29
DOI:10.1073/pnas.2205498119
语种:English
出版社:The National Academy of Sciences of the United States of America
摘要:Significance
Peptides are selected and bound to HLA-I within the endoplasmic reticulum, aided by the molecular chaperone tapasin. HLA-I allotypes vary in their dependence on tapasin for peptide loading, and tapasin-independent allotypes present a more diverse set of peptides than tapasin-dependent allotypes. We show that imputed
TAPBP messenger RNA-expression levels, along with HLA-I allotype-specific tapasin dependence level, associate with malaria outcome. High
TAPBP expression significantly associated with protection amongst individuals with tapasin-dependent HLA allotypes relative to low tapasin expression. Tapasin expression had no effect on tapasin-independent allotypes, which conferred protection regardless of imputed tapasin-expression levels. Thus, intrinsically high tapasin-expression levels may compensate for the restrictive nature of HLA-I tapasin dependence in the peptide-loading process, attenuating the course of malaria.
HLA class I (HLA-I) allotypes vary widely in their dependence on tapasin (TAPBP), an integral component of the peptide-loading complex, to present peptides on the cell surface. We identified two single-nucleotide polymorphisms that regulate
TAPBP messenger RNA (mRNA) expression in Africans,
rs111686073 (
G/
C) and
rs59097151 (A/
G), located in an AP-2α transcription factor binding site and a microRNA (miR)-4486 binding site, respectively.
rs111686073G and
rs59097151A induced significantly higher
TAPBP mRNA expression relative to the alternative alleles due to higher affinity for AP-2α and abrogation of miR-4486 binding, respectively. These variants associated with lower
Plasmodium falciparum parasite prevalence and lower incidence of clinical malaria specifically among individuals carrying tapasin-dependent HLA-I allotypes, presumably by augmenting peptide loading, whereas tapasin-independent allotypes associated with relative protection, regardless of imputed
TAPBP mRNA expression levels. Thus, an attenuated course of malaria may occur through enhanced breadth and/or magnitude of antigen presentation, an important consideration when evaluating vaccine efficacy.