학술논문

FCRL5 Delineates Functionally Impaired Memory B Cells Associated with Plasmodium falciparum Exposure.
Document Type
article
Source
PLoS pathogens. 11(5)
Subject
B-Lymphocytes
Cells
Cultured
Cell Line
Animals
Humans
Mice
Plasmodium falciparum
Malaria
Falciparum
Receptors
Fc
Recombinant Proteins
Antigens
Protozoan
Cohort Studies
Gene Expression Profiling
Endemic Diseases
Immunologic Memory
Gene Expression Regulation
Adult
Child
Caregivers
Uganda
Asymptomatic Diseases
Virology
Microbiology
Immunology
Medical Microbiology
Language
Abstract
Exposure to Plasmodium falciparum is associated with circulating "atypical" memory B cells (atMBCs), which appear similar to dysfunctional B cells found in HIV-infected individuals. Functional analysis of atMBCs has been limited, with one report suggesting these cells are not dysfunctional but produce protective antibodies. To better understand the function of malaria-associated atMBCs, we performed global transcriptome analysis of these cells, obtained from individuals living in an area of high malaria endemicity in Uganda. Comparison of gene expression data suggested down-modulation of B cell receptor signaling and apoptosis in atMBCs compared to classical MBCs. Additionally, in contrast to previous reports, we found upregulation of Fc receptor-like 5 (FCRL5), but not FCRL4, on atMBCs. Atypical MBCs were poor spontaneous producers of antibody ex vivo, and higher surface expression of FCRL5 defined a distinct subset of atMBCs compromised in its ability to produce antibody upon stimulation. Moreover, higher levels of P. falciparum exposure were associated with increased frequencies of FCRL5+ atMBCs. Together, our findings suggest that FCLR5+ identifies a functionally distinct, and perhaps dysfunctional, subset of MBCs in individuals exposed to P. falciparum.