Immunopathogenesis of alphaviruses

Abstract

Alphaviruses, members of the enveloped, positive-sense, single-stranded RNA Togaviridae family, represent a reemerging public health threat as mosquito vectors expand into new geographic territories. The Old World alphaviruses, which include chikungunya virus, Ross River virus, and Sindbis virus, tend to cause a clinical syndrome characterized by fever, rash, and arthritis, whereas the New World alphaviruses, which consist of Venezuelan equine encephalitis virus, eastern equine encephalitis virus, and western equine encephalitis virus, induce encephalomyelitis. Following recovery from the acute phase of infection, many patients are left with debilitating persistent joint and neurological complications that can last for years. Clues from human cases and studies using animal models strongly suggest that much of the disease and pathology induced by alphavirus infection, particularly atypical and chronic manifestations, is mediated by the immune system rather than directly by the virus. This review discusses the current understanding of the immunopathogenesis of the arthritogenic and neurotropic alphaviruses accumulated through both natural infection of humans and experimental infection of animals, particularly mice. As treatment following alphavirus infection is currently limited to supportive care, understanding the contribution of the immune system to the disease process is critical to developing safe and effective therapies.

Keywords: Alphavirus; Chikungunya virus; Immune response; Immunopathogenesis; Pathogenesis; Sindbis virus.

Fig. 1

Geographic range of cases of human disease induced by select Old World (CHIKV, RRV, and SINV) and New World (VEEV, EEEV, and WEEV) alphaviruses. CHIKV = chikungunya virus, RRV = Ross River virus, SINV = Sindbis virus, VEEV = Venezuelan equine encephalitis virus, EEEV = eastern equine encephalitis virus, WEEV = western equine encephalitis virus.