Abstract

Chikungunya disease (CHIKD) is a viral infection caused by an alphavirus, chikungunya virus (CHIKV), and triggers large outbreaks leading to epidemics. Despite the low mortality rate, it is a major public health concern owing to high morbidity in affected individuals. The complete spectrum of this disease can be divided into four phases based on its clinical presentation and immunopathology. When a susceptible individual is bitten by an infected mosquito, the bite triggers inflammatory responses attracting neutrophils and initiating a cascade of events, resulting in the entry of the virus into permissive cells. This phase is termed the pre-acute or the intrinsic incubation phase. The virus utilizes the cellular components of the innate immune system to enter into circulation and reach primary sites of infection such as the lymph nodes, spleen, and liver. Also, at this point, antigen-presenting cells (APCs) present the viral antigens to the T cells thereby activating and initiating adaptive immune responses. This phase is marked by the exhibition of clinical symptoms such as fever, rashes, arthralgia, and myalgia and is termed the acute phase of the disease. Viremia reaches its peak during this phase, thereby enhancing the antigen-specific host immune response. Simultaneously, T cell-mediated activation of B cells leads to the formation of CHIKV specific antibodies. Increase in titres of neutralizing IgG/IgM antibodies results in the clearance of virus from the bloodstream and marks the initiation of the post-acute phase. Immune responses mounted during this phase of the infection determine the degree of disease progression or its resolution. Some patients may progress to a chronic arthritic phase of the disease that may last from a few months to several years, owing to a compromised disease resolution. The present review discusses the immunopathology of CHIKD and the factors that dictate disease progression and its resolution.

Highlights

  • Chikungunya disease (CHIKD), caused by an arthritogenic alphavirus, chikungunya virus (CHIKV), is becoming a major public health hazard [1, 2]

  • The monocyte/macrophage infiltrates were replaced by an enhanced neutrophil infiltration, followed by eosinophils infiltrates as well [83]. These results suggest that neutrophils are one of the key mediators of arthritic symptoms and tissue damage in CHIKV infection by releasing granules carrying antimicrobial molecules and producing reactive oxygen species (ROS) due to an oxidative burst, which is a well-established feature of neutrophils in other models of inflammation [84, 85]

  • Chikungunya disease resolution is a combination of viral clearance from the host and resolution of inflammation, as all the major symptoms witnessed by the CHIKD patients are due to the robust pro-inflammatory host response

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Summary

INTRODUCTION

Chikungunya disease (CHIKD), caused by an arthritogenic alphavirus, chikungunya virus (CHIKV), is becoming a major public health hazard [1, 2]. CHIKD is primarily a viral infection manifested as a fever with severe arthritic joint involvement. Components of adaptive immunity have been reported to be instrumental in mounting the severity of the disease and resulting in the chronic arthritic condition that could last for years [26, 31, 32]. The current review is a chronological compilation of the immunopathological events that take place during the acute and post-acute phases of CHIKD that may either lead to resolution of the disease or contribute to an exaggerated immune response, resulting in a full-blown arthritic chronic phase lasting up-to several years (Figure 1)

Early Events Leading to the Establishment of CHIKV Infection
Establishment of the Acute Phase of Infection
Immunopathology of Acute Phase
CHIKV Clearance
Disease Resolution
CHRONIC PHASE
CONCLUSION
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