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. 2009 Dec 15;3(2):205-9.
doi: 10.4172/1747-0862.1000036.

Acquired heterosubtypic antibodies in human immunity for avian H5N1 influenza

Acquired heterosubtypic antibodies in human immunity for avian H5N1 influenza

Garry W Lynch et al. J Mol Genet Med. .

Abstract

Well understood are the adaptive and dramatic neutralizing homosubtypic antibody responses to hypervariable, immunodominant sites of the hemagglutinin (HA) and neuraminidase (NA) of individual influenza strains. These define influenza subtypes and vaccines modelled upon their HA and NA antigens provide seasonal neutralizing antibody protection against subsequent exposure to the strain and its close relatives, but give little if any protection against antigenically drifted or shifted strains. Contrasting to this is a different form of acquired antibody response, called heterosubtypic immunity. This provides a more seasoned adaptive antibody response to immune-recessive epitopes that are highly-conserved amongst strains. Although, such responses are of lower individual amplitudes than seasonal mechanisms they are active across influenza subtypes, and may give pre-emptive protection against new strains yet to emerge. Heterosubtypic immunities have been well studied in animals, but surprisingly there is minimal evidence for this type of antibody immunity in humans. Thus championed is the notion that seasoned humoral responses can through repeated exposure to sites widely conserved across different strains, cumulatively provide humans with a level of broad protection against emergent novel strains, such as H5N1, that is not afforded by seasonal humoral responses.

Keywords: H1N1; H5N1; Influenza; antibody; heterosubtypic; immunity; pandemic.

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Conflict of interest statement

None declared.

Figures

Figure 1.
Figure 1.
Schematic representation of the humoral and cell-mediated systems of heterosubtypic immunity for the delivery of cross-strain protection of novel influenzas, such as avian H5N1, via the targeting of cell-free virions and influenza protein expressing infected-cells. Both arms work in concert to protect against viral infection and propagation, pathogenesis and death. Shown is an overview of the respective mechanisms, the proteins they target, evidence of their cross-protective power, and avenues for the development of heterosubtypic-based vaccine and antiviral interventions for broad based influenza protection. [References: Jameson et al, 1999; Tumpey et al, 2001; Kong et al, 2006; Luke et al, 2006; Ichinohe et al, 2007; Roy et al, 2007; Sandlbute et al, 2007; Simmons et al, 2007; Zhou et al, 2007; Carragher et al, 2008; Gioia et al, 2008; Kayshap et al, 2008; Kreitz et al, 2008; Lee et al, 2008; Lynch et al, 2008; Roti et al, 2008; Stelzer-Braid et al, 2008]

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