Plasmacytoid dendritic cell activation by foot‐and‐mouth disease virus requires immune complexes

L Guzylack‐Piriou, F Bergamin… - European journal of …, 2006 - Wiley Online Library
L Guzylack‐Piriou, F Bergamin, M Gerber, KC McCullough, A Summerfield
European journal of immunology, 2006Wiley Online Library
Natural IFN‐producing cells (NIPC), also called plasmacytoid dendritic cells, represent an
essential component of the innate immune defense against infection. Despite this, not much
is known about the pathways involved in their activation by non‐enveloped viruses. The
present study demonstrates that the non‐enveloped foot‐and‐mouth disease virus (FMDV)
cannot stimulate IFN‐α responses in NIPC, unless complexed with FMDV‐specific
immunoglobulins. Stimulation of NIPC with such immune complexes employs FcγRII …
Abstract
Natural IFN‐producing cells (NIPC), also called plasmacytoid dendritic cells, represent an essential component of the innate immune defense against infection. Despite this, not much is known about the pathways involved in their activation by non‐enveloped viruses. The present study demonstrates that the non‐enveloped foot‐and‐mouth disease virus (FMDV) cannot stimulate IFN‐α responses in NIPC, unless complexed with FMDV‐specific immunoglobulins. Stimulation of NIPC with such immune complexes employs FcγRII ligation, leading to strong secretion of IFN‐α. In contrast to the stimulation of NIPC by many enveloped viruses, FMDV induction of IFN‐α production requires live virus. It is necessary for the virus to initiate its replicative cycle. Moreover, it is an abortive replication, as witnessed by the decrease of dsRNA levels and viral titers with time post infection. Sensitivity of the NIPC stimulation to wortmannin and chloroquin, but not leupeptin, indicates an essential role for the pre‐lysosomal stage endosomal compartment. In conclusion, the present study demonstrates that immune complexes provide the means for a non‐interferogenic virus to induce IFN‐α responses by NIPC. This indicates an important link between NIPC and antibodies in immune responses against non‐enveloped viruses such as FMDV.
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