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Commentary

First evidence of a pro-inflammatory response to severe infection with influenza virus H1N1

Isabel Fernández de Castro, María Guzmán-Fulgencio, Mónica García-Álvarez and Salvador Resino*

Author Affiliations

Centro Nacional de Microbiología, Instituto de Salud Carlos III (Campus Majadahonda); Carretera Majadahonda-Pozuelo, Km 2.2; 28220 Majadahonda (Madrid), Spain

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Critical Care 2010, 14:115  doi:10.1186/cc8846


See related research by Bermejo-Martin et al., http://ccforum.com/content/13/6/R201, related letter by Krstíc, http://ccforum.com/content/14/2/410 and related letter by Kawashima et al., http://ccforum.com/content/14/2/411

The electronic version of this article is the complete one and can be found online at: http://ccforum.com/content/14/1/115


Published:11 February 2010

© 2010 BioMed Central Ltd

Abstract

The great majority of infections caused by the pandemic variant of the influenza virus (nvH1N1) are self-limited, but a small percentage of patients develop severe symptoms requiring hospitalization. Bermejo-Martin and colleagues have presented a pilot study describing the differences in the early immune response for patients both mildly and severely infected with nvH1N1. Patients who develop severe symptoms after nvH1N1 infection showed Th1 and Th17 'hypercytokinemia', compared to mildly infected patients and healthy controls. The mediators involved with the Th1 and Th17 profiles are known to be involved in antiviral, pro-inflammatory and autoimmune responses. This is the first work reporting the association of a pro-inflamatory immune response with a severe pandemic infection, although it is likely that more studies are needed to understand the detrimental or beneficial roles these cytokines play in the evolution of mild and severe nvH1N1 infection.

Commentary

In a recent article for Critical Care, Bermejo-Martin and colleagues [1] describe Th1 and Th17 hypercytokinemia as an early signature host response to severe infection by the pandemic variant of the influenza virus (nvH1N1). The nvH1N1 infection is usually self-limiting in nature, but some patients develop severe symptoms requiring hospitalization [2]. The host immune response may play an important role in poor outcomes after infection. The human host immune response to nvH1N1 infection is unknown at this time and studies on its contribution to disease pathogenesis are desperately needed to improve prevention and treatment strategies.

By analyzing 29 cytokines and chemokines and the hemagglutination inhibition activity, Bermejo-Martin and colleagues [1] assessed the early host innate and adaptive immune responses in patients both mildly and severely infected with nvH1N1. While infection with nvH1N1 induces a typical innate response in both mild and severe cases, severe infections with respiratory involvement are characterized by an early secretion of Th17 and Th1 cytokines. Thus, hospitalized patients tend to show high systemic levels of mediators that stimulate Th17 (IL-8, IL-9, IL-17, IL-6) and Th1 responses (IFN-γ, TNF-α, IL-15, IL-12p70) [1]. Based on this finding, this study was able to highlight similarities between the cytokine response to severe H1N1 infection and the pathogenesis of asthma and some autoimmune diseases.

The Th1 response is primarily involved with host immune defense against intracellular pathogens by activating cellular immunity. This response is effective in eradicating infectious agents such as viruses [3]. Indeed, Th1 cells produce IFN-γ and cytokines that are involved in monocyte/macrophage-mediated inflammatory responses [4]. When the Th1 response is exhaustively prolonged, it may result in host damage. Moreover, other authors have reported that Th1-dominated responses may be implicated in the pathogenesis of autoimmune disorders and chronic inflammatory diseases [5]. Bermejo-Martin and colleagues [1] found IL-15, IL-12p70, and IL-6 to be particularly elevated following severe nvH1N1 infection. These three cytokines are known to mediate both antiviral and pro-inflammatory responses. The authors [1] also found a significant inverse relationship of IL-6 and IL-8 with the pressure of oxygen in arterial blood in severely infected patients. Interestingly, previous studies had already reported high levels of specific proinflammatory cytokines and chemokines in severe SARS coronavirus, H5N1 and respiratory syncytial virus infections [6-11].

Th17 cells are required for host defense against intracellular pathogens [12]. Th17 promotes inflammation by inducing various pro-inflammatory cytokines and chemokines, recruiting neutrophils, enhancing antibody production, and activating T cells [12]. Th17 cells secrete IL-17, IL-17F, and IL-22, thereby inducing a massive tissue reaction. Also, these cells secrete IL-21 to communicate with the cells of the immune system [13]. However, uncontrolled production of these cytokines induces tissue damage in infected tissues [12]. In addition, Th17 cells have a well-known role in clearing pathogens during infections and inducing tissue inflammation in autoimmune disease [13]. Interestingly, the key role of IL-17 and its receptor in the immunopathology of influenza infection in a mouse model has just recently been reported [14].

Taken together, these findings show that severe pandemic H1N1 infection is characterized by early elevation of key immune pro-inflammatory mediators participating in both Th1 and Th17 inflammatory responses. This pro-inflammatory response may be the cause of the severe respiratory symptoms caused by nvH1N1 infection. However, the authors also provide an alternative version of the story: Th1 and Th17 cytokines may reflect a vigorous antiviral host response necessary for viral clearance. This article [1] is the first that describes an association between severe influenza infection and a Th17 response in humans. The researchers correctly bring up the fact that a better understanding of the immune response to the new H1N1 virus could contribute to the design of more effective therapies. Similarly, the results of this study reinforce the importance of early treatment with antivirals in those patients with high risk factors, such as pregnancy, asthma, and obesity, among others, to avoid triggering unwanted inflammatory phenomena, which could explain the appearance of pneumonia in these patients. The results of this work also support the study of drugs that modulate the immune response in the treatment of this disease [15]. Moreover, the study of genetic polymorphisms of relevant genes involved in the development of Th1 and Th17 immune responses in severely infected patients could be of interest, since these polymorphisms could strongly influence gene expression.

Further studies would help to understand the harmful or beneficial roles that these cytokines play in the evolution of mild and severe nvH1N1 infection. But this report confirms that Th1 and Th17 responses are distinctive hallmarks of severe respiratory compromise following nvH1N1 infection.

Abbreviations

IFN: interferon gamma; IL: interleukin; nvH1N1: new variant of H1N1 influenza virus; TNF: tumor necrosis factor.

Competing interests

The authors declare that they have no competing interests.

Acknowledgements

This work was supported by grants from Instituto de Salud Carlos III (PI08/0738; UIPY 1467/07) to SR. MG-F is supported by a grant of Instituto de Salud Carlos III (CM09/00031). MG-A is supported by a grant of Instituto de Salud Carlos III (CM08/00101).

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