{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,1]],"date-time":"2026-10-01T09:30:34Z","timestamp":1790847034316,"version":"4.1.0"},"reference-count":30,"publisher":"Springer Science and Business Media LLC","issue":"3","license":[{"start":{"date-parts":[[2014,6,20]],"date-time":"2014-06-20T00:00:00Z","timestamp":1403222400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0"},{"start":{"date-parts":[[2014,6,20]],"date-time":"2014-06-20T00:00:00Z","timestamp":1403222400000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0"}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["Crit Care"],"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Introduction<\/jats:title>\n                    <jats:p>Inherited variability in host immune responses influences susceptibility and outcome of Influenza A virus (IAV) infection, but these factors remain largely unknown. Components of the innate immune response may be crucial in the first days of the infection. The collectins surfactant protein (SP)-A1, -A2, and -D and mannose-binding lectin (MBL) neutralize IAV infectivity, although only SP-A2 can establish an efficient neutralization of poorly glycosylated pandemic IAV strains.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      We studied the role of polymorphic variants at the genes of MBL (\n                      <jats:italic>MBL2<\/jats:italic>\n                      ), SP-A1 (\n                      <jats:italic>SFTPA1<\/jats:italic>\n                      ), SP-A2 (\n                      <jats:italic>SFTPA2<\/jats:italic>\n                      ), and SP-D (\n                      <jats:italic>SFTPD<\/jats:italic>\n                      ) in 93 patients with H1N1 pandemic 2009 (H1N1pdm) infection.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Multivariate analysis showed that two frequent\n                      <jats:italic>SFTPA2<\/jats:italic>\n                      missense alleles (rs1965708-\n                      <jats:italic>C<\/jats:italic>\n                      and rs1059046-\n                      <jats:italic>A<\/jats:italic>\n                      ) and the\n                      <jats:italic>SFTPA2<\/jats:italic>\n                      haplotype\n                      <jats:italic>1A<\/jats:italic>\n                      <jats:sup>\n                        <jats:italic>0<\/jats:italic>\n                      <\/jats:sup>\n                      were associated with a need for mechanical ventilation, acute respiratory failure, and acute respiratory distress syndrome. The\n                      <jats:italic>SFTPA2<\/jats:italic>\n                      haplotype\n                      <jats:italic>1A<\/jats:italic>\n                      <jats:sup>\n                        <jats:italic>1<\/jats:italic>\n                      <\/jats:sup>\n                      was a protective variant. Kaplan-Meier analysis and Cox regression also showed that diplotypes not containing the\n                      <jats:italic>1A<\/jats:italic>\n                      <jats:sup>\n                        <jats:italic>1<\/jats:italic>\n                      <\/jats:sup>\n                      haplotype were associated with a significantly shorter time to ICU admission in hospitalized patients. In addition, rs1965708-\n                      <jats:italic>C<\/jats:italic>\n                      (\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u20090.0007), rs1059046-\n                      <jats:italic>A<\/jats:italic>\n                      (\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u20090.0007), and haplotype\n                      <jats:italic>1A<\/jats:italic>\n                      <jats:sup>\n                        <jats:italic>0<\/jats:italic>\n                      <\/jats:sup>\n                      (\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u20090.0004) were associated, in a dose-dependent fashion, with lower PaO\n                      <jats:sub>2<\/jats:sub>\n                      \/FiO\n                      <jats:sub>2<\/jats:sub>\n                      ratio, whereas haplotype\n                      <jats:italic>1A<\/jats:italic>\n                      <jats:sup>\n                        <jats:italic>1<\/jats:italic>\n                      <\/jats:sup>\n                      was associated with a higher PaO\n                      <jats:sub>2<\/jats:sub>\n                      \/FiO\n                      <jats:sub>2<\/jats:sub>\n                      ratio (\n                      <jats:italic>P<\/jats:italic>\n                      \u2009=\u20090.001).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      Our data suggest an effect of genetic variants of\n                      <jats:italic>SFTPA2<\/jats:italic>\n                      on the severity of H1N1pdm infection and could pave the way for a potential treatment with haplotype-specific (\n                      <jats:italic>1A<\/jats:italic>\n                      <jats:sup>\n                        <jats:italic>1<\/jats:italic>\n                      <\/jats:sup>\n                      ) SP-A2 for future IAV pandemics.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1186\/cc13934","type":"journal-article","created":{"date-parts":[[2014,6,20]],"date-time":"2014-06-20T05:04:00Z","timestamp":1403240640000},"update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":57,"title":["Surfactant protein A genetic variants associate with severe respiratory insufficiency in pandemic influenza A virus infection"],"prefix":"10.1186","volume":"18","author":[{"given":"Estefan\u00eda","family":"Herrera-Ramos","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Marta","family":"L\u00f3pez-Rodr\u00edguez","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jos\u00e9 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