Figure 1.

An overview of current knowledge of innate and adaptive responses in immunobiology of CCHFV infection (see accompanying Table 6). (1) Whether infection is via tick bite (A) or mucosal exposure (B), the initial events, including virus trafficking from the site of infection and dissemination to other organs, are poorly understood. Tissue damage is likely a combination of direct infection (2), inflammatory innate responses (3), and killing of infected cells by activated adaptive immune cells (4). Upon infection (2), many host and viral proteins are engaged to promote and limit viral replication. Host sensors that detect infection and initiate innate responses are not well understood and host proteins that act as restriction factors largely remain to be identified. Although type I IFN response is likely a key determinant of disease outcome and infection rapidly becomes resistant to type I IFN-mediated restriction, how virus blocks or resists type I IFN is largely unknown. Additionally, CCHFV possesses proteins with both pro- and anti-apoptotic function, suggesting apoptosis modulation may be a key factor in pathogenesis. Innate cell responses likely play a key early role in disease outcome (3). Infected innate cells can produce pro-inflammatory cytokines that recruit inflammatory cells, further contributing to tissue injury. Innate immune cells such as macrophages and dendritic cells can be infected, although whether they are important for controlling the virus through IFN production, antigen presentation, or reactive oxygen species production is unclear. Cells appear to only become partially activated in response to infection, and whether virus directly inhibits full activation resulting in improper antigen presentation requires further study. (4) Lastly, the role of adaptive immunity in controlling infection warrants further study. Neutralizing antibodies are not necessary for protection, yet other critical effector functions of antibody responses remain to be determined. The role of T-cells is even less clear. It is unknown if CD4 T-helper activity is required for support of B- and CD8-T-cell responses; cytotoxic activity of NK and/or CD8 T-cells is required for controlling virus; T-cells control CCHFV through production of antiviral cytokines; or virus-infected cells resist cytotoxic effector cells through actively blocking host cell apoptosis.