Acquired heterosubtypic antibodies in human immunity for avian H5N1 influenza
Identifieur interne : 000D93 ( Pmc/Corpus ); précédent : 000D92; suivant : 000D94Acquired heterosubtypic antibodies in human immunity for avian H5N1 influenza
Auteurs : Garry W. Lynch ; Paul Selleck ; John S. SullivanSource :
- Journal of Molecular and Genetic Medicine : An International Journal of Biomedical Research [ 1747-0862 ] ; 2009.
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.
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PubMed: 20076792
PubMed Central: 2805841
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PMC:2805841Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Acquired heterosubtypic antibodies in human immunity for avian H5N1 influenza</title><author><name sortKey="Lynch, Garry W" sort="Lynch, Garry W" uniqKey="Lynch G" first="Garry W" last="Lynch">Garry W. Lynch</name><affiliation><nlm:aff id="aff1">Biosafety, Immunobiology, Global Health and Pandemic Infections Research, Central Clinical School, Faculties of Medicine</nlm:aff></affiliation><affiliation><nlm:aff id="aff2">Veterinary Science, The University of Sydney, Camperdown, NSW 2006, Australia</nlm:aff></affiliation><affiliation><nlm:aff id="aff3">Cellular and Molecular Pathology Research Unit, Oral Pathology and Oral Medicine, Westmead Centre for Oral Health, Westmead Hospital and Faculty of Dentistry, University of Sydney, Westmead, NSW 2145, Australia</nlm:aff></affiliation></author><author><name sortKey="Selleck, Paul" sort="Selleck, Paul" uniqKey="Selleck P" first="Paul" last="Selleck">Paul Selleck</name><affiliation><nlm:aff id="aff4">The Australian Animal Health Laboratories, CSIRO, Geelong, Vic 3219, Australia</nlm:aff></affiliation></author><author><name sortKey="Sullivan, John S" sort="Sullivan, John S" uniqKey="Sullivan J" first="John S" last="Sullivan">John S. Sullivan</name><affiliation><nlm:aff id="aff1">Biosafety, Immunobiology, Global Health and Pandemic Infections Research, Central Clinical School, Faculties of Medicine</nlm:aff></affiliation><affiliation><nlm:aff id="aff5">Children's Cancer Institute Australia for Medical Research, Randwick, NSW 2031, Australia</nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">20076792</idno><idno type="pmc">2805841</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2805841</idno><idno type="RBID">PMC:2805841</idno><date when="2009">2009</date><idno type="wicri:Area/Pmc/Corpus">000D93</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000D93</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Acquired heterosubtypic antibodies in human immunity for avian H5N1 influenza</title><author><name sortKey="Lynch, Garry W" sort="Lynch, Garry W" uniqKey="Lynch G" first="Garry W" last="Lynch">Garry W. Lynch</name><affiliation><nlm:aff id="aff1">Biosafety, Immunobiology, Global Health and Pandemic Infections Research, Central Clinical School, Faculties of Medicine</nlm:aff></affiliation><affiliation><nlm:aff id="aff2">Veterinary Science, The University of Sydney, Camperdown, NSW 2006, Australia</nlm:aff></affiliation><affiliation><nlm:aff id="aff3">Cellular and Molecular Pathology Research Unit, Oral Pathology and Oral Medicine, Westmead Centre for Oral Health, Westmead Hospital and Faculty of Dentistry, University of Sydney, Westmead, NSW 2145, Australia</nlm:aff></affiliation></author><author><name sortKey="Selleck, Paul" sort="Selleck, Paul" uniqKey="Selleck P" first="Paul" last="Selleck">Paul Selleck</name><affiliation><nlm:aff id="aff4">The Australian Animal Health Laboratories, CSIRO, Geelong, Vic 3219, Australia</nlm:aff></affiliation></author><author><name sortKey="Sullivan, John S" sort="Sullivan, John S" uniqKey="Sullivan J" first="John S" last="Sullivan">John S. Sullivan</name><affiliation><nlm:aff id="aff1">Biosafety, Immunobiology, Global Health and Pandemic Infections Research, Central Clinical School, Faculties of Medicine</nlm:aff></affiliation><affiliation><nlm:aff id="aff5">Children's Cancer Institute Australia for Medical Research, Randwick, NSW 2031, Australia</nlm:aff></affiliation></author></analytic><series><title level="j">Journal of Molecular and Genetic Medicine : An International Journal of Biomedical Research</title><idno type="eISSN">1747-0862</idno><imprint><date when="2009">2009</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>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.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Bui, Hh" uniqKey="Bui H">HH Bui</name></author><author><name sortKey="Peters, B" uniqKey="Peters B">B Peters</name></author><author><name sortKey="Assarsson, E" uniqKey="Assarsson E">E Assarsson</name></author><author><name sortKey="Mbawuike, I" uniqKey="Mbawuike I">I Mbawuike</name></author><author><name sortKey="Sette, A" uniqKey="Sette A">A Sette</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Carragher, Dm" uniqKey="Carragher D">DM Carragher</name></author><author><name sortKey="Kaminski, Da" uniqKey="Kaminski D">DA 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<front><journal-meta><journal-id journal-id-type="nlm-ta">J Mol Genet Med</journal-id><journal-id journal-id-type="publisher-id">jmgm</journal-id><journal-title-group><journal-title>Journal of Molecular and Genetic Medicine : An International Journal of Biomedical Research</journal-title></journal-title-group><issn pub-type="epub">1747-0862</issn><publisher><publisher-name>Library Publishing Media</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">20076792</article-id><article-id pub-id-type="pmc">2805841</article-id><article-categories><subj-group subj-group-type="heading"><subject>Minireview</subject></subj-group></article-categories><title-group><article-title>Acquired heterosubtypic antibodies in human immunity for avian H5N1 influenza</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Lynch</surname><given-names>Garry W</given-names></name><xref ref-type="aff" rid="aff1">1</xref><xref ref-type="aff" rid="aff2">2</xref><xref ref-type="aff" rid="aff3">3</xref><xref ref-type="corresp" rid="cor1">*</xref></contrib><contrib contrib-type="author"><name><surname>Selleck</surname><given-names>Paul</given-names></name><xref ref-type="aff" rid="aff4">4</xref></contrib><contrib contrib-type="author"><name><surname>Sullivan</surname><given-names>John S</given-names></name><xref ref-type="aff" rid="aff1">1</xref><xref ref-type="aff" rid="aff5">5</xref></contrib><aff id="aff1"><label>1</label>Biosafety, Immunobiology, Global Health and Pandemic Infections Research, Central Clinical School, Faculties of Medicine</aff><aff id="aff2"><label>2</label>Veterinary Science, The University of Sydney, Camperdown, NSW 2006, Australia</aff><aff id="aff3"><label>3</label>Cellular and Molecular Pathology Research Unit, Oral Pathology and Oral Medicine, Westmead Centre for Oral Health, Westmead Hospital and Faculty of Dentistry, University of Sydney, Westmead, NSW 2145, Australia</aff><aff id="aff4"><label>4</label>The Australian Animal Health Laboratories, CSIRO, Geelong, Vic 3219, Australia</aff><aff id="aff5"><label>5</label>Children's Cancer Institute Australia for Medical Research, Randwick, NSW 2031, Australia</aff></contrib-group><author-notes><corresp id="cor1"><label>*</label>Correspondance to: Garry Lynch, <email>garry_lynch@optusnet.com.au</email>, Tel: +61 2 9519 8151, Fax: +61 2 9519 8151</corresp></author-notes><pub-date pub-type="collection"><month>12</month><year>2009</year></pub-date><pub-date pub-type="epub"><day>15</day><month>12</month><year>2009</year></pub-date><volume>3</volume><issue>2</issue><fpage>205</fpage><lpage>209</lpage><history><date date-type="received"><day>31</day><month>8</month><year>2009</year></date><date date-type="rev-recd"><day>07</day><month>12</month><year>2009</year></date><date date-type="accepted"><day>09</day><month>12</month><year>2009</year></date></history><permissions><copyright-statement>© The Authors</copyright-statement><copyright-year>2009</copyright-year><license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by-nc/2.0/uk/"><license-p>This is an open access article, published under the terms of the Creative Commons Attribution Non-Commercial License (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by-nc/2.0/uk/">http://creativecommons.org/licenses/by-nc/2.0/uk/</ext-link>). This license permits non-commercial use, distribution and reproduction of the article, provided the original work is appropriately acknowledged with correct citation details.</license-p></license></permissions><abstract><p>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.</p></abstract><kwd-group><kwd>Influenza</kwd><kwd>H5N1</kwd><kwd>H1N1</kwd><kwd>pandemic</kwd><kwd>immunity</kwd><kwd>heterosubtypic</kwd><kwd>antibody</kwd></kwd-group></article-meta></front><body><sec sec-type="intro"><title>INTRODUCTION</title><p>With a mortality up to 250 times greater than strains that cause epidemics the lethality of the 1918 avian H1N1 influenza pandemic is frequently reported (<xref ref-type="bibr" rid="B28">Palese et al, 2006</xref>; <xref ref-type="bibr" rid="B44">Taubenberger and Morens, 2006</xref>), but seldom appreciated is the fact that the majority (>97%) of those infected survived, amounting to 0.8-2 billion lives recovered. The most profound defence against influenza is provided by adaptive immunity that is mediated by neutralizing strain-specific “seasonal” antibodies directed against highly variable naïve antigens of an infecting influenza. But this is a post-emergent process that optimally takes weeks to months for full development (<xref ref-type="bibr" rid="B27">Murphy et al, 1982</xref>; <xref ref-type="bibr" rid="B3">Couch and Kasel, 1983</xref>; <xref ref-type="bibr" rid="B8">Edwards et al, 1986</xref>), and consequently beyond the time-frame of primary infection, viral shedding and disease development and is incapable of protecting against the first appearance of a new influenza strain. Therefore, additional mechanisms of protection need to be invoked to explain the mass herd immune protection of the community. Clearly, innate and heterosubtypic cellular immune mechanisms are involved in this; however, these alone are insufficient to justify this level of protection against a pandemic influenza, and prompt the issue of whether acquired heterotypic antibody immunity may provide a missing link in immune protection. Heterosubtypic cellular and antibody immune responses have been realized and studied for almost fifty years (<xref ref-type="bibr" rid="B20">Kilbuorne and Schulman, 1965</xref>), with extensive examination in animal models of influenza infection (reviewed in, <xref ref-type="bibr" rid="B11">Epstein, 2003</xref>; <xref ref-type="bibr" rid="B14">Grebe et al, 2008</xref>). There has been considerable study and demonstration of heterosubtypic cell-mediated immunity in humans as an essential component of systematic immune protection, and recent evaluation of its cross-protective vaccine potential (<xref ref-type="bibr" rid="B7">Doherty and Kelso, 2008</xref>). However, this is not the focus of this present review. In striking contrast to cell-mediated responses, until recently, there has been minimal study or direct evidence for heterosubtypic antibody immunity in humans, or resolution of protective heterosubtypic antibodies, or their partnering conserved influenza epitopes (<italic>i.e.</italic>, protectopes; <xref ref-type="bibr" rid="B29">Plotnicky-Gilquin et al, 1999</xref>) (<xref ref-type="bibr" rid="B1">Bui et al, 2007</xref>; <xref ref-type="bibr" rid="B9">Ekiert et al, 2009</xref>; <xref ref-type="bibr" rid="B43">Sui et al, 2009</xref>). It is, therefore, proposed that akin to the heterosubtypic processes shown in animals, human antibody memories become acquired with age, from repeated infections and stimulus by highly-conserved influenza antigens. Despite being immunorecessive, this systematically leads to a broad “seasoned” heterosubtypic protection from antibodies that target equivalent sites of new strains. Thus it is important to identify whether or not such core antibody responses across influenzas do in fact provide significant immune protection against novel influenzas, such as avian H5N1 and evolving 2009 H1N1.</p><p>H5N1 influenza has had a higher measured mortality than the 1918 H1N1 influenza, albeit with recovery of approximately 40% of individuals surviving infection. Epidemiologic studies indicate an age-related protection with survival of approximately 60% of individuals over the age of 40 years compared to less than 25% for individuals in the 10-20 years age group (<xref ref-type="bibr" rid="B39">Smallman-Raynor and Cliff, 2007</xref>). Similarly data from the 1918 H1N1 and 1957 H2N2 pandemics also indicate a greater level of protection in adults (<xref ref-type="bibr" rid="B24">Luk et al, 2001</xref>; <xref ref-type="bibr" rid="B12">Epstein, 2006</xref>), which may have reduced the impact in the adult sub-population older than 65 years to that of seasonal epidemics. While apparent protection of the elderly may result from earlier immunization of this cohort from exposure to a like virus, we believe it is equally plausible to result from a lifetime acquired heterosubtypic immunity, or even a combination of both. As seasonal antibodies provide the main correlate of homotypic neutralizing protection against influenza (<xref ref-type="bibr" rid="B36">Schild et al, 1975</xref>; <xref ref-type="bibr" rid="B48">Virelizier, 1975</xref>; <xref ref-type="bibr" rid="B6">Delem and Jovanovic, 1978</xref>; <xref ref-type="bibr" rid="B18">Kashyap et al, 2008</xref>), we now raise the question of whether seasoned, cross-reactive antibodies similarly provide a significant contribution for heterosubtypic protection. Certainly, our own findings implicate a pre-existing pool of anti-influenza antibodies in an unexposed Australian population that can protect against avian H5N1 influenza, <italic>in vitro</italic>, along with H5-hemagglutinin binding antibodies that are most prominent with adult age (<xref ref-type="bibr" rid="B26">Lynch et al, 2008</xref>; <xref ref-type="bibr" rid="B40">Stelzer-Braid et al, 2008</xref>). This is also supported by observations of cross-reactive anti-neuraminidase antibodies from unexposed humans that partially protect H5N1 infected mice (<xref ref-type="bibr" rid="B35">Sandbulte et al, 2007</xref>). The idea of a role for low levels of pre-existing crosstypic antibodies in some humans to protect against foreign emerging influenza strains is indeed attractive. This would be supported by the other arm of heterosubtypic immunity, namely human cross-typic cell-mediated immunity, for which there is far more substantial evidence of protection against H5N1 pathogenesis and death (<xref ref-type="bibr" rid="B17">Jameson et al, 1999</xref>; <xref ref-type="bibr" rid="B22">Kreijtz et al, 2008</xref>; <xref ref-type="bibr" rid="B23">Lee et al, 2008</xref>; <xref ref-type="bibr" rid="B32">Roti et al 2008</xref>). A general overview of the combined human cellular and humoral system arms of heterosubtypic immunity and support evidence is provided in <xref ref-type="fig" rid="F1">Figure 1</xref>.</p><fig id="F1" position="float"><label>Figure 1.</label><caption><p>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: <xref ref-type="bibr" rid="B17">Jameson et al, 1999</xref>; <xref ref-type="bibr" rid="B46">Tumpey et al, 2001</xref>; <xref ref-type="bibr" rid="B21">Kong et al, 2006</xref>; <xref ref-type="bibr" rid="B25">Luke et al, 2006</xref>; <xref ref-type="bibr" rid="B16">Ichinohe et al, 2007</xref>; <xref ref-type="bibr" rid="B33">Roy et al, 2007</xref>; <xref ref-type="bibr" rid="B35">Sandlbute et al, 2007</xref>; <xref ref-type="bibr" rid="B38">Simmons et al, 2007</xref>; <xref ref-type="bibr" rid="B50">Zhou et al, 2007</xref>; <xref ref-type="bibr" rid="B2">Carragher et al, 2008</xref>; <xref ref-type="bibr" rid="B13">Gioia et al, 2008</xref>; <xref ref-type="bibr" rid="B18">Kayshap et al, 2008</xref>; <xref ref-type="bibr" rid="B22">Kreitz et al, 2008</xref>; <xref ref-type="bibr" rid="B23">Lee et al, 2008</xref>; <xref ref-type="bibr" rid="B26">Lynch et al, 2008</xref>; <xref ref-type="bibr" rid="B32">Roti et al, 2008</xref>; <xref ref-type="bibr" rid="B40">Stelzer-Braid et al, 2008</xref>]</p></caption><graphic xlink:href="jmgm-03-205-g001"></graphic></fig><p>The indication that heterosubtypic H5N1 neutralizing antibodies in unexposed individuals could be bolstered by a seasonal vaccine (<xref ref-type="bibr" rid="B13">Gioia et al, 2008</xref>) is encouraging. However, in general seasonal vaccines have not been reported to give wider immunity for emerging strains, such as the avian H5N1, or the 2009 H1N1 pandemic influenzas (<xref ref-type="bibr" rid="B19">Kelly and Grant, 2009</xref>). We believe that this marked discrepancy is mainly due to the nature and size of the protective responses. Seasonal vaccines promote a substantial neutralizing response, mainly directed against the globular head region of hemagglutinin (HA) for cell receptor binding and neuraminidase (NA) for viral egress from an infected cell. In contrast, seasoned responses would by definition promote many lesser responses to multiple protein sites, including most, if not all, surface and interior proteins of influenza viruses. We predict this would individually go undetected, or be in the ‘grey zone’ of current <italic>in vitro</italic> assays. However, we propose that the net effect of marshalling the combined heterosubtypic systems responses would result in <italic>in vivo</italic> protection that could be measured and modelled. As a result we suggest that although seasonal and seasoned responses may appear discordant they would effectively champion one another, and ultimately enable both specific and universal protective capabilities to ideally reduce the debilitating and lethal effects of influenza to at least one of mild illness.</p><p>The requirements for vaccines to promote heterosubtypic antibody responses to conserved sites of influenza proteins for broad, seasoned, possibly universal protection would need to be inherently different from current seasonal vaccines: The latter express hypervariable determinants and promote high-tire antibody responses to homotypic immune dominant determinants of the HA globular-head to block cell receptor binding and neutralize infection. The challenge therefore is to separately design seasoned vaccines capable of promoting broad heterosubtypic protection against drifted and new zoonotic (avian) strains. Unlike seasonal vaccines that disrupt influenza-cell binding, a combination of seasoned vaccine approaches would likely be required to stimulate both antibody and T-cell responses to multiple conserved epitopes widely expressed across human and avian (<italic>e.g.</italic>, H5N1) influenzas, and be accessible to antibodies or drugs to disrupt all aspects of the infection. Valuable insights into conserved linear and conformational antibody and T-cell epitopes of human and avian influenza proteins (<italic>e.g.</italic>, HA, NA, M2) are tabulated in the bioinformatic studies of 7 H1N1, 8 H3N2 and 2 H5N1 isolates (<xref ref-type="bibr" rid="B1">Bui et al, 2007</xref>). In this analysis remarkably all but one Ab-epitope study was from animal experiments, but since then additional human antibody protectopes are being realized (<xref ref-type="bibr" rid="B9">Ekiert et al, 2009</xref>; <xref ref-type="bibr" rid="B43">Sui et al, 2009</xref>). This study was followed by a more encompassing evaluation of highly-conserved linear sites of 9 amino acids or longer, across all the strains of influenza (<xref ref-type="bibr" rid="B15">Heiny et al, 2007</xref>). Both studies revealed considerable conservation of sequence and antigen epitopes across the breadth of influenza proteins, with some 90 to 100% conserved and some already identified from animal studies as protective determinants (<xref ref-type="bibr" rid="B1">Bui et al, 2007</xref>). For seasoned vaccine initiatives the mapping and <italic>in vivo</italic> evaluation of epitope combinations for multiple-point targeting of infection is now necessary for vaccine design.</p><p>Examples of protective antibodies against conserved epitopes include those binding to the M2 protein tetrameric ectodomain (<xref ref-type="bibr" rid="B5">De Filette et al, 2008</xref>), site(s) on NA that disrupt sialidase release of budding virons from infected cells (<xref ref-type="bibr" rid="B35">Sandbulte et al, 2007</xref>) and of the HA stem that contains the proteolytic cleavage site and hydrophobic membrane fusion segment (<xref ref-type="bibr" rid="B1">Bui et al, 2007</xref>; <xref ref-type="bibr" rid="B43">Sui et al, 2009</xref>; <xref ref-type="bibr" rid="B9">Ekiert et al, 2009</xref>)<italic>.</italic> In natural infections and vaccine antibody responses the conserved but poorly-immunogenic sites of the HA stalk must compete with the highly-immunogenic and variable epitopes of the globular-head. Recent studies have shown the broadly protective value of human antibodies that target the pre-fusion structures of the HA stalk (<xref ref-type="bibr" rid="B9">Ekiert et al, 2009</xref>; <xref ref-type="bibr" rid="B43">Sui et al, 2009</xref>). As cross-protective antibodies to the conserved stalk are developed in mice following immunization with constructs with deleted globular-head but not with complete HA, studies are now needed to evaluate heterotypic humoral responses to a variety of conserved influenza epitopes in the absence of competing HA immune-dominant globular-head antigens (<xref ref-type="bibr" rid="B34">Sagawa et al, 1996</xref>). More contentious is what role if any do antibodies directed at internal influenza antigens, such as in the highly-conserved NP protein, play in hetero(sub)typic protection. NP is expressed on the surface of influenza infected cells (<xref ref-type="bibr" rid="B47">Virelizier et al, 1977</xref>; <xref ref-type="bibr" rid="B41">Stitz et al, 1990</xref>; <xref ref-type="bibr" rid="B31">Prokudina and Semenova, 1991</xref>) and is a major target for cytotoxic T-lymphocytes (<xref ref-type="bibr" rid="B41">Stitz et al, 1990</xref>; <xref ref-type="bibr" rid="B31">Prokudina and Semenova, 1991</xref>). However, early studies indicated that NP did not protect against influenza infection (<xref ref-type="bibr" rid="B41">Stitz et al, 1990</xref>). Substantial antibody responses are generated to internal proteins by natural infection or vaccination (<xref ref-type="bibr" rid="B4">Couch, 2003</xref>). In mice, following vaccination with recombinant NP, both non-neutralizing and protective anti-NP antibodies are generated that reduce influenza virus titres and reduce mortality in influenza-infected mice passively treated with NP hyperimmune serum (<xref ref-type="bibr" rid="B2">Carragher et al, 2008</xref>). Similarly in a chicken study model, passively transferred anti-NP antibodies (and to a lesser extent antibodies to the polymerase complex proteins PA1, PB1, PB2) were found to protect against infection with highly-pathogenic H7N3 influenza (<xref ref-type="bibr" rid="B37">Shahzad et al, 2008</xref>). It is important to determine if such responses are translatable to humans, and what role anti-NP antibodies play in heterosubtypic protection elicited by NP vaccines (<xref ref-type="bibr" rid="B10">Epstein et al, 2005</xref>; <xref ref-type="bibr" rid="B30">Price et al, 2009</xref>). It is also of interest to evaluate whether antibodies to infected cells expressing internal viral antigens, such as NP, may add to and complement other cross-typic responses (<italic>e.g.</italic>, to M2e and HA stalk/fusion domains).</p><p>Whether the rules of engagement and responses to the generation of protective heterosubtypic antibodies in humans mirror well-characterized immunodominant homotypic responses remains to be determined. Certainly a significant unknown is how to best present protectope antigens for vaccines to stimulate protective heterosubtypic antibody responses. This would be governed by a variety of factors, including the optimal selection of protein or peptide constructs, epitope combinations, presentation (<italic>e.g.</italic>, with or without adjuvant) (<xref ref-type="bibr" rid="B42">Straight et al, 2008</xref>), route of administration (<xref ref-type="bibr" rid="B30">Price et al, 2009</xref>) and roles of antibody secreting plasma cell and memory B cell responses (<xref ref-type="bibr" rid="B49">Wrammert et al, 2008</xref>). The first point of order, however, needs to be a clear demonstration of the role and significance of heterosubtypic antibodies in cross-typic protection of humans for influenza. Certainly the exciting findings of <xref ref-type="bibr" rid="B9">Ekiert et al (2009)</xref> and <xref ref-type="bibr" rid="B43">Sui et al (2009)</xref> indicate the potential, but this needs to be further supported by a more comprehensive evaluation of the complement of conserved influenza epitopes.</p><p>Thus, for more universal protection new approaches are required to target the many sites that are conserved across influenza proteins. However, because the immune responses to those sites are subverted by immune-dominant HA, and to a lesser extent NA antigens that form the centre-point of seasonal vaccines, new style constructs are needed that actually avoid those immunodominant sites. It would therefore be informative to examine heterosubtypic antibody responses for multiple viral constructs devoid of the regions that are the main focus of seasonal vaccines. The challenge is to test and evaluate a broad sampling of conserved influenza epitope combinations, including already indicated antibody protectopes, to substantiate the value of seasoned heterosubtypic antibody responses in broad protection of drifted and shifted influenzas. Studies of linear conserved regions can be made using recombinant protein fragments, peptides or DNA constructs before graduating to conformationally maintained recombinant and native viral protein constructs for the more difficult study of discontinuous conserved epitopes. Cross-strain antibody immune response comparisons of seasonal inactivated and live attenuated vaccines versus seasoned conserved antigen constructs will reveal the differences and similarities in their capacities for heterosubtypic protection to drive future vaccine initiatives. We envisage that if true value can be unequivocally established, future seasoned protectope vaccines will be used for the population at large to separately complement not replace current seasonal strategies. Together, these vaccines will systematically provide antibody protection to reduce the impact of emerging pathogenic and pandemic influenzas and reduce the considerable health and economic burden of epidemic influenzas. With comprehensive and synergistic targeting of conserved antibody epitopes in conjunction with strategies already raised for stimulating heterosubtypic T-cell responses (<xref ref-type="bibr" rid="B7">Doherty and Kelso, 2008</xref>; <xref ref-type="bibr" rid="B23">Lee et al, 2008</xref>) we are confident that vaccines for sustained and synergistic crosstypic influenza protection will be realized. Continued evolution and expansion of avian to human H5N1 and human to human 2009 H1N1 pandemic H1N1 virus, highlights the need for more universal vaccines to generate heterotypic protection for immune-naive individuals, and promote rapid heterosubtypic hyperimmune responses for passive therapies to meet ongoing and future challenges.</p></sec></body><back><ack><title>ACKNOWLEDGEMENTS</title><p>This work was partially supported by a University of Sydney Bridging Support Grant.</p></ack><fn-group><title>COMPETING INTERESTS</title><fn fn-type="conflict"><p>None declared.</p></fn></fn-group><ref-list><title>REFERENCES</title><ref id="B1"><element-citation publication-type="journal"><person-group 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