Single Nucleotide Polymorphisms in the Human Leukocyte Antigen Region Are Associated With Hemagglutination Inhibition Antibody Response to Influenza Vaccine
Background: The annual death associated with seasonal influenza is 290,000–650,000 globally, which can be effectively reduced by influenza vaccination. However, the protective hemagglutination inhibition (HAI) antibody response to influenza vaccine is affected by many factors, among which single nuc...
Saved in:
Published in | Frontiers in genetics Vol. 13; p. 790914 |
---|---|
Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
07.02.2022
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Background:
The annual death associated with seasonal influenza is 290,000–650,000 globally, which can be effectively reduced by influenza vaccination. However, the protective hemagglutination inhibition (HAI) antibody response to influenza vaccine is affected by many factors, among which single nucleotide polymorphisms (SNPs) in the human leukocyte antigen (HLA) region can alter the antigen-presenting function of the HLA molecule, thus influencing the process of antibody mounting against vaccine antigen.
Methods:
Healthy subjects of the Han nationality were recruited and received seasonal trivalent influenza vaccine. Paired serum samples collected on and approximately 28 days after vaccination were tested in parallel by HAI assays. HLA alleles related to the immune response to influenza vaccine reported in the previous literature were summarized, and six corresponding tag SNPs were selected and genotyped using the MassARRAY technology platform.
Results:
The effects of HLA SNPs on HAI antibody response to influenza vaccine varied with different vaccine antigens. The AA genotype of rs41547618 was correlated with low A/H1N1-specific antibody titer compared with the GG + GA genotype (
p
= .007). The TT genotype of rs17885382 was correlated with low A/H3N2-specific antibody titer compared with the CC + CT genotype (
p
= .003). In addition, haplotype consisting of rs41542812—rs17885382—rs2068205—rs41547618—rs6905837—rs9270299—CCTGCA was correlated with non-responsiveness to influenza vaccine (OR = 2.39, 95% CI = 1.02–5.62).
Conclusion:
HLA SNPs were associated with HAI antibody response to influenza vaccine, which can help in a better understanding of the varied responsiveness to influenza vaccine in the population. |
---|---|
AbstractList | Background: The annual death associated with seasonal influenza is 290,000-650,000 globally, which can be effectively reduced by influenza vaccination. However, the protective hemagglutination inhibition (HAI) antibody response to influenza vaccine is affected by many factors, among which single nucleotide polymorphisms (SNPs) in the human leukocyte antigen (HLA) region can alter the antigen-presenting function of the HLA molecule, thus influencing the process of antibody mounting against vaccine antigen. Methods: Healthy subjects of the Han nationality were recruited and received seasonal trivalent influenza vaccine. Paired serum samples collected on and approximately 28 days after vaccination were tested in parallel by HAI assays. HLA alleles related to the immune response to influenza vaccine reported in the previous literature were summarized, and six corresponding tag SNPs were selected and genotyped using the MassARRAY technology platform. Results: The effects of HLA SNPs on HAI antibody response to influenza vaccine varied with different vaccine antigens. The AA genotype of rs41547618 was correlated with low A/H1N1-specific antibody titer compared with the GG + GA genotype (p = .007). The TT genotype of rs17885382 was correlated with low A/H3N2-specific antibody titer compared with the CC + CT genotype (p = .003). In addition, haplotype consisting of rs41542812-rs17885382-rs2068205-rs41547618-rs6905837-rs9270299-CCTGCA was correlated with non-responsiveness to influenza vaccine (OR = 2.39, 95% CI = 1.02-5.62). Conclusion: HLA SNPs were associated with HAI antibody response to influenza vaccine, which can help in a better understanding of the varied responsiveness to influenza vaccine in the population.Background: The annual death associated with seasonal influenza is 290,000-650,000 globally, which can be effectively reduced by influenza vaccination. However, the protective hemagglutination inhibition (HAI) antibody response to influenza vaccine is affected by many factors, among which single nucleotide polymorphisms (SNPs) in the human leukocyte antigen (HLA) region can alter the antigen-presenting function of the HLA molecule, thus influencing the process of antibody mounting against vaccine antigen. Methods: Healthy subjects of the Han nationality were recruited and received seasonal trivalent influenza vaccine. Paired serum samples collected on and approximately 28 days after vaccination were tested in parallel by HAI assays. HLA alleles related to the immune response to influenza vaccine reported in the previous literature were summarized, and six corresponding tag SNPs were selected and genotyped using the MassARRAY technology platform. Results: The effects of HLA SNPs on HAI antibody response to influenza vaccine varied with different vaccine antigens. The AA genotype of rs41547618 was correlated with low A/H1N1-specific antibody titer compared with the GG + GA genotype (p = .007). The TT genotype of rs17885382 was correlated with low A/H3N2-specific antibody titer compared with the CC + CT genotype (p = .003). In addition, haplotype consisting of rs41542812-rs17885382-rs2068205-rs41547618-rs6905837-rs9270299-CCTGCA was correlated with non-responsiveness to influenza vaccine (OR = 2.39, 95% CI = 1.02-5.62). Conclusion: HLA SNPs were associated with HAI antibody response to influenza vaccine, which can help in a better understanding of the varied responsiveness to influenza vaccine in the population. Background: The annual death associated with seasonal influenza is 290,000–650,000 globally, which can be effectively reduced by influenza vaccination. However, the protective hemagglutination inhibition (HAI) antibody response to influenza vaccine is affected by many factors, among which single nucleotide polymorphisms (SNPs) in the human leukocyte antigen (HLA) region can alter the antigen-presenting function of the HLA molecule, thus influencing the process of antibody mounting against vaccine antigen.Methods: Healthy subjects of the Han nationality were recruited and received seasonal trivalent influenza vaccine. Paired serum samples collected on and approximately 28 days after vaccination were tested in parallel by HAI assays. HLA alleles related to the immune response to influenza vaccine reported in the previous literature were summarized, and six corresponding tag SNPs were selected and genotyped using the MassARRAY technology platform.Results: The effects of HLA SNPs on HAI antibody response to influenza vaccine varied with different vaccine antigens. The AA genotype of rs41547618 was correlated with low A/H1N1-specific antibody titer compared with the GG + GA genotype (p = .007). The TT genotype of rs17885382 was correlated with low A/H3N2-specific antibody titer compared with the CC + CT genotype (p = .003). In addition, haplotype consisting of rs41542812—rs17885382—rs2068205—rs41547618—rs6905837—rs9270299—CCTGCA was correlated with non-responsiveness to influenza vaccine (OR = 2.39, 95% CI = 1.02–5.62).Conclusion: HLA SNPs were associated with HAI antibody response to influenza vaccine, which can help in a better understanding of the varied responsiveness to influenza vaccine in the population. The annual death associated with seasonal influenza is 290,000-650,000 globally, which can be effectively reduced by influenza vaccination. However, the protective hemagglutination inhibition (HAI) antibody response to influenza vaccine is affected by many factors, among which single nucleotide polymorphisms (SNPs) in the human leukocyte antigen (HLA) region can alter the antigen-presenting function of the HLA molecule, thus influencing the process of antibody mounting against vaccine antigen. Healthy subjects of the Han nationality were recruited and received seasonal trivalent influenza vaccine. Paired serum samples collected on and approximately 28 days after vaccination were tested in parallel by HAI assays. HLA alleles related to the immune response to influenza vaccine reported in the previous literature were summarized, and six corresponding tag SNPs were selected and genotyped using the MassARRAY technology platform. The effects of HLA SNPs on HAI antibody response to influenza vaccine varied with different vaccine antigens. The AA genotype of rs41547618 was correlated with low A/H1N1-specific antibody titer compared with the GG + GA genotype ( = .007). The TT genotype of rs17885382 was correlated with low A/H3N2-specific antibody titer compared with the CC + CT genotype ( = .003). In addition, haplotype consisting of rs41542812-rs17885382-rs2068205-rs41547618-rs6905837-rs9270299-CCTGCA was correlated with non-responsiveness to influenza vaccine (OR = 2.39, 95% CI = 1.02-5.62). HLA SNPs were associated with HAI antibody response to influenza vaccine, which can help in a better understanding of the varied responsiveness to influenza vaccine in the population. Background: The annual death associated with seasonal influenza is 290,000–650,000 globally, which can be effectively reduced by influenza vaccination. However, the protective hemagglutination inhibition (HAI) antibody response to influenza vaccine is affected by many factors, among which single nucleotide polymorphisms (SNPs) in the human leukocyte antigen (HLA) region can alter the antigen-presenting function of the HLA molecule, thus influencing the process of antibody mounting against vaccine antigen. Methods: Healthy subjects of the Han nationality were recruited and received seasonal trivalent influenza vaccine. Paired serum samples collected on and approximately 28 days after vaccination were tested in parallel by HAI assays. HLA alleles related to the immune response to influenza vaccine reported in the previous literature were summarized, and six corresponding tag SNPs were selected and genotyped using the MassARRAY technology platform. Results: The effects of HLA SNPs on HAI antibody response to influenza vaccine varied with different vaccine antigens. The AA genotype of rs41547618 was correlated with low A/H1N1-specific antibody titer compared with the GG + GA genotype ( p = .007). The TT genotype of rs17885382 was correlated with low A/H3N2-specific antibody titer compared with the CC + CT genotype ( p = .003). In addition, haplotype consisting of rs41542812—rs17885382—rs2068205—rs41547618—rs6905837—rs9270299—CCTGCA was correlated with non-responsiveness to influenza vaccine (OR = 2.39, 95% CI = 1.02–5.62). Conclusion: HLA SNPs were associated with HAI antibody response to influenza vaccine, which can help in a better understanding of the varied responsiveness to influenza vaccine in the population. |
Author | Wang, Dayan Zhong, Shuyi Li, Mao Wei, Hejiang Wen, Simin Cheng, Yanhui Shu, Yuelong |
AuthorAffiliation | 1 School of Public Health (Shenzhen) , Shenzhen Campus of Sun Yat-sen University , Shenzhen , China 2 Institute for Viral Disease Control and Prevention , Chinese Center for Disease Prevention and Control , Beijing , China |
AuthorAffiliation_xml | – name: 2 Institute for Viral Disease Control and Prevention , Chinese Center for Disease Prevention and Control , Beijing , China – name: 1 School of Public Health (Shenzhen) , Shenzhen Campus of Sun Yat-sen University , Shenzhen , China |
Author_xml | – sequence: 1 givenname: Shuyi surname: Zhong fullname: Zhong, Shuyi – sequence: 2 givenname: Hejiang surname: Wei fullname: Wei, Hejiang – sequence: 3 givenname: Mao surname: Li fullname: Li, Mao – sequence: 4 givenname: Yanhui surname: Cheng fullname: Cheng, Yanhui – sequence: 5 givenname: Simin surname: Wen fullname: Wen, Simin – sequence: 6 givenname: Dayan surname: Wang fullname: Wang, Dayan – sequence: 7 givenname: Yuelong surname: Shu fullname: Shu, Yuelong |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/35198005$$D View this record in MEDLINE/PubMed |
BookMark | eNp1UtuO0zAQjdAi9sJ-AC_Ij7y0-JbEeUGqVkArVYC4Plq2M0m9OHY3dpC638LH4ra7aBcJv3g0c86ZseecFyc-eCiKFwTPGRPN664HD3OKKZ3XDW4If1KckariM4EpOXkQnxaXMV7jfHjDGOPPilNWkkZgXJ4Vv79Y3ztAHybjICTbAvoU3G4I43Zj4xCR9ShtAC2nQXm0hulnMLsEaOGTzQOgz9Db4NFizKkYg7EqQYt-2LRBSxhU37spWa_SHrTyG6vtIdzTdWh3mR-3wUdAKeR65ybwtwp9V8ZYD8-Lp51yES7v7ovi27u3X6-Ws_XH96urxXpmeFWmmRBtSRTr8guBNxgLQrTRusS17nRLTMOxotxgQXMRMphRrjHlLdeVIjWwi2J11G2Dupbb0Q5q3MmgrDwkwthLNSabf0jiRvNaKUU6rDjOIWtJU4LQeRROgWatN0et7aQHaA34NCr3SPRxxduN7MMvKUSZB62zwKs7gTHcTBCTHGw04JzyEKYoacWowKUQOENfPuz1t8n9ejOgPgLMGGIcoZPGpsMycmvrJMFy7yV58JLce0kevZSZ5B_mvfj_OX8AEd3QfQ |
CitedBy_id | crossref_primary_10_3390_v15040906 crossref_primary_10_7774_cevr_2024_13_2_105 |
Cites_doi | 10.1038/ng.3576 10.3390/biology9120467 10.1016/j.vaccine.2012.12.026 10.1016/j.vaccine.2014.01.057 10.1016/j.vaccine.2008.07.065 10.1093/infdis/167.3.584 10.1038/sj.clpt.6100415 10.1093/hmg/ddt317 10.1080/21645515.2017.1338547 10.1371/journal.pone.0071376 10.1038/nature01911 10.1016/j.cels.2020.06.009 10.1186/s13073-018-0568-8 10.1016/S0140-6736(17)33293-2 10.1016/S1081-1206(10)61931-X 10.2165/00129785-200404050-00002 10.1182/blood-2015-02-628800 10.1086/338014 10.1038/nature01912 10.1080/21645515.2015.1119345 |
ContentType | Journal Article |
Copyright | Copyright © 2022 Zhong, Wei, Li, Cheng, Wen, Wang and Shu. Copyright © 2022 Zhong, Wei, Li, Cheng, Wen, Wang and Shu. 2022 Zhong, Wei, Li, Cheng, Wen, Wang and Shu |
Copyright_xml | – notice: Copyright © 2022 Zhong, Wei, Li, Cheng, Wen, Wang and Shu. – notice: Copyright © 2022 Zhong, Wei, Li, Cheng, Wen, Wang and Shu. 2022 Zhong, Wei, Li, Cheng, Wen, Wang and Shu |
DBID | AAYXX CITATION NPM 7X8 5PM DOA |
DOI | 10.3389/fgene.2022.790914 |
DatabaseName | CrossRef PubMed MEDLINE - Academic PubMed Central (Full Participant titles) DOAJ Directory of Open Access Journals |
DatabaseTitle | CrossRef PubMed MEDLINE - Academic |
DatabaseTitleList | MEDLINE - Academic PubMed CrossRef |
Database_xml | – sequence: 1 dbid: DOA name: DOAJ Directory of Open Access Journals url: https://www.doaj.org/ sourceTypes: Open Website – sequence: 2 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Biology |
DocumentTitleAlternate | Zhong et al |
EISSN | 1664-8021 |
ExternalDocumentID | oai_doaj_org_article_09b47aaa1f0a4047a3d195e8bc4642e2 PMC8859407 35198005 10_3389_fgene_2022_790914 |
Genre | Journal Article |
GrantInformation_xml | – fundername: ; grantid: kqtd20180411143323605 – fundername: ; grantid: 8204100563 |
GroupedDBID | 53G 5VS 9T4 AAFWJ AAKDD AAYXX ACGFS ACXDI ADBBV ADRAZ AFPKN ALMA_UNASSIGNED_HOLDINGS AOIJS BAWUL BCNDV CITATION DIK EMOBN GROUPED_DOAJ GX1 HYE KQ8 M48 M~E OK1 PGMZT RNS RPM IAO IEA IHR IPNFZ ISR NPM RIG 7X8 5PM |
ID | FETCH-LOGICAL-c465t-88d51a3f000e4900811bcbb507bfbd1c940a24c082900e8d5324b024d4b6a17e3 |
IEDL.DBID | M48 |
ISSN | 1664-8021 |
IngestDate | Wed Aug 27 01:29:25 EDT 2025 Thu Aug 21 14:36:00 EDT 2025 Thu Jul 10 22:48:27 EDT 2025 Thu Jan 02 22:54:59 EST 2025 Tue Jul 01 01:45:02 EDT 2025 Thu Apr 24 22:56:57 EDT 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Keywords | influenza vaccine single nucleotide polymorphisms human leukocyte antigen hemagglutination inhibition antibody genetic epidemiology |
Language | English |
License | Copyright © 2022 Zhong, Wei, Li, Cheng, Wen, Wang and Shu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c465t-88d51a3f000e4900811bcbb507bfbd1c940a24c082900e8d5324b024d4b6a17e3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Reviewed by: Ming Zhang, Shenzhen University, China Zanxian Xia, Central South University, China Edited by: Zhenjian Zhuo, Guangzhou Medical University, China This article was submitted to Applied Genetic Epidemiology, a section of the journal Frontiers in Genetics |
OpenAccessLink | http://journals.scholarsportal.info/openUrl.xqy?doi=10.3389/fgene.2022.790914 |
PMID | 35198005 |
PQID | 2632805880 |
PQPubID | 23479 |
ParticipantIDs | doaj_primary_oai_doaj_org_article_09b47aaa1f0a4047a3d195e8bc4642e2 pubmedcentral_primary_oai_pubmedcentral_nih_gov_8859407 proquest_miscellaneous_2632805880 pubmed_primary_35198005 crossref_citationtrail_10_3389_fgene_2022_790914 crossref_primary_10_3389_fgene_2022_790914 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2022-02-07 |
PublicationDateYYYYMMDD | 2022-02-07 |
PublicationDate_xml | – month: 02 year: 2022 text: 2022-02-07 day: 07 |
PublicationDecade | 2020 |
PublicationPlace | Switzerland |
PublicationPlace_xml | – name: Switzerland |
PublicationTitle | Frontiers in genetics |
PublicationTitleAlternate | Front Genet |
PublicationYear | 2022 |
Publisher | Frontiers Media S.A |
Publisher_xml | – name: Frontiers Media S.A |
References | Rehman (B19) 2007; 16 Castro-Santos (B1) 2020; 9 Poland (B15) 2008; 26 Posteraro (B17) 2014; 32 Gelder (B5) 2002; 185 Kalpaklıoğlu (B9) 2002; 89 Linnik (B11) 2016; 12 Poland (B16) 2007; 82 Castrucci (B2) 2018; 14 Weidinger (B21) 2013; 22 Guermonprez (B6) 2003; 425 Houde (B7) 2003; 425 Liu (B12) 2020; 11 Moss (B13) 2013; 8 Iuliano (B8) 2018; 391 B3 Scepanovic (B20) 2018; 10 Fernandez (B4) 2015; 126 Zhou (B22) 2016; 48 Narwaney (B14) 2013; 31 Powers (B18) 1993; 167 Lambkin (B10) 2004; 4 |
References_xml | – volume: 48 start-page: 740 year: 2016 ident: B22 article-title: Deep Sequencing of the MHC Region in the Chinese Population Contributes to Studies of Complex Disease publication-title: Nat. Genet. doi: 10.1038/ng.3576 – volume: 9 start-page: 467 year: 2020 ident: B1 article-title: HLA-DRB1*07:01 and *08:02 Alleles Confer a Protective Effect against ACPA-Positive Rheumatoid Arthritis in a Latin American Admixed Population publication-title: Biology doi: 10.3390/biology9120467 – volume: 31 start-page: 1123 year: 2013 ident: B14 article-title: Association of HLA Class II Genes with Clinical Hyporesponsiveness to Trivalent Inactivated Influenza Vaccine in Children publication-title: Vaccine doi: 10.1016/j.vaccine.2012.12.026 – volume: 32 start-page: 1661 year: 2014 ident: B17 article-title: The Link between Genetic Variation and Variability in Vaccine Responses: Systematic Review and Meta-Analyses publication-title: Vaccine doi: 10.1016/j.vaccine.2014.01.057 – volume: 26 start-page: D35 year: 2008 ident: B15 article-title: Immunogenetics of Seasonal Influenza Vaccine Response publication-title: Vaccine doi: 10.1016/j.vaccine.2008.07.065 – volume: 167 start-page: 584 year: 1993 ident: B18 article-title: Effect of Age on Cytotoxic T Lymphocyte Memory as Well as Serum and Local Antibody Responses Elicited by Inactivated Influenza Virus Vaccine publication-title: J. Infect. Dis. doi: 10.1093/infdis/167.3.584 – ident: B3 – volume: 82 start-page: 653 year: 2007 ident: B16 article-title: Heterogeneity in Vaccine Immune Response: the Role of Immunogenetics and the Emerging Field of Vaccinomics publication-title: Clin. Pharmacol. Ther. doi: 10.1038/sj.clpt.6100415 – volume: 22 start-page: 4841 year: 2013 ident: B21 article-title: A Genome-wide Association Study of Atopic Dermatitis Identifies Loci with Overlapping Effects on Asthma and Psoriasis publication-title: Hum. Mol. Genet. doi: 10.1093/hmg/ddt317 – volume: 14 start-page: 637 year: 2018 ident: B2 article-title: Factors Affecting Immune Responses to the Influenza Vaccine publication-title: Hum. Vaccin. Immunother. doi: 10.1080/21645515.2017.1338547 – volume: 8 start-page: e71376 year: 2013 ident: B13 article-title: Correlation between Human Leukocyte Antigen Class II Alleles and HAI Titers Detected post-influenza Vaccination publication-title: PLoS One doi: 10.1371/journal.pone.0071376 – volume: 16 start-page: 300 year: 2007 ident: B19 article-title: Human Leukocyte Antigen (HLA) Class II Association with Rheumatic Heart Disease in Pakistan publication-title: J. Heart Valve Dis. – volume: 425 start-page: 397 year: 2003 ident: B6 article-title: ER-phagosome Fusion Defines an MHC Class I Cross-Presentation Compartment in Dendritic Cells publication-title: Nature doi: 10.1038/nature01911 – volume: 11 start-page: 131 year: 2020 ident: B12 article-title: Computationally Optimized SARS-CoV-2 MHC Class I and II Vaccine Formulations Predicted to Target Human Haplotype Distributions publication-title: Cel Syst. doi: 10.1016/j.cels.2020.06.009 – volume: 10 start-page: 1 year: 2018 ident: B20 article-title: Human Genetic Variants and Age Are the Strongest Predictors of Humoral Immune Responses to Common Pathogens and Vaccines publication-title: Genome Med. doi: 10.1186/s13073-018-0568-8 – volume: 391 start-page: 1285 year: 2018 ident: B8 article-title: Estimates of Global Seasonal Influenza-Associated Respiratory Mortality: a Modelling Study publication-title: Lancet doi: 10.1016/S0140-6736(17)33293-2 – volume: 89 start-page: 155 year: 2002 ident: B9 article-title: Possible Association between Cockroach Allergy and HLA Class II Antigens publication-title: Ann. Allergy Asthma Immunol. doi: 10.1016/S1081-1206(10)61931-X – volume: 4 start-page: 293 year: 2004 ident: B10 article-title: Human Genetics and Responses to Influenza Vaccination publication-title: Am. J. PharmacoGenomics doi: 10.2165/00129785-200404050-00002 – volume: 126 start-page: 69 year: 2015 ident: B4 article-title: Genome-wide Analysis Links NFATC2 with Asparaginase Hypersensitivity publication-title: Blood doi: 10.1182/blood-2015-02-628800 – volume: 185 start-page: 114 year: 2002 ident: B5 article-title: Associations between Human Leukocyte Antigens and Nonresponsiveness to Influenza Vaccine publication-title: J. Infect. Dis. doi: 10.1086/338014 – volume: 425 start-page: 402 year: 2003 ident: B7 article-title: Phagosomes Are Competent Organelles for Antigen Cross-Presentation publication-title: Nature doi: 10.1038/nature01912 – volume: 12 start-page: 907 year: 2016 ident: B11 article-title: Impact of Host Genetic Polymorphisms on Vaccine Induced Antibody Response publication-title: Hum. Vaccin. Immunother. doi: 10.1080/21645515.2015.1119345 |
SSID | ssj0000493334 |
Score | 2.2835894 |
Snippet | Background:
The annual death associated with seasonal influenza is 290,000–650,000 globally, which can be effectively reduced by influenza vaccination.... The annual death associated with seasonal influenza is 290,000-650,000 globally, which can be effectively reduced by influenza vaccination. However, the... Background: The annual death associated with seasonal influenza is 290,000-650,000 globally, which can be effectively reduced by influenza vaccination.... Background: The annual death associated with seasonal influenza is 290,000–650,000 globally, which can be effectively reduced by influenza vaccination.... |
SourceID | doaj pubmedcentral proquest pubmed crossref |
SourceType | Open Website Open Access Repository Aggregation Database Index Database Enrichment Source |
StartPage | 790914 |
SubjectTerms | genetic epidemiology Genetics hemagglutination inhibition antibody human leukocyte antigen influenza vaccine single nucleotide polymorphisms |
SummonAdditionalLinks | – databaseName: DOAJ Directory of Open Access Journals dbid: DOA link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Lb9QwELZQJSQuiDfhJSNxQgpNYidOjgVRLQhVCCj0Zo0f6aZsk6qbPSy_hR_LjJ2udhGCC7dVYmet-SaZb-LJN4y9APBVW2B2oqrSptJVkFI3h1S1wmausqDaUG1xVM2O5fuT8mSr1RfVhEV54Gi4_awxUgFA3mYgM_wpXN6UvjZWInX24emLMW8rmTqLvFcIIeM2JmZhzX6LeJAsZlG8Ug1OkDuBKOj1_4lk_l4ruRV8Dm-xmxNr5AdxtbfZNd_fYddjH8n1XfbzMwaghedHJE48jJ3z_OOwwKwejdgtz5e86zkSPR7e2PMPfvV9sOvR84N-JDFO_slTVTJeHg9NcHnHv3XjnM_8OZyeknvG14b8XT_vTKjzCtPN4NY4PxTaej4OeD50PfkB_CtY2rW_x44P3355M0untgspmrQc07p2ZQ6iRSt62RBnyI01BomjaY3LbSMzKKSlj3JxBA5GTmYw1DtpKsiVF_fZXj_0_iHjiFYlDCDFKoRUxiIXknkDwggkbkpCwrIrDLSdNMmpNcZCY25CsOkAmybYdIQtYS83Uy6iIMffBr8mYDcDSUs7HEAP05OH6X95WMKeX7mFxnuPNlSg98NqqUnrvs5KfAQm7EF0k81fUeNDJONlwtSOA-2sZfdM382Dvnddl2hj9eh_LP4xu0H2CHXm6gnbGy9X_inSqNE8C3fML4_6HbM priority: 102 providerName: Directory of Open Access Journals |
Title | Single Nucleotide Polymorphisms in the Human Leukocyte Antigen Region Are Associated With Hemagglutination Inhibition Antibody Response to Influenza Vaccine |
URI | https://www.ncbi.nlm.nih.gov/pubmed/35198005 https://www.proquest.com/docview/2632805880 https://pubmed.ncbi.nlm.nih.gov/PMC8859407 https://doaj.org/article/09b47aaa1f0a4047a3d195e8bc4642e2 |
Volume | 13 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3fb9MwELbGEBIviPFrGWwyEk9IGUnsxMkDQgMxCoIJAYW-RWfHacO6ZGtTifK38Mdy56QVRRVPvERRYqfRnZ37zr5-H2NPAGxSRpidqCQ2viwS8EnNwVelMEGRGFClq7Y4SwZD-W4Uj3bYSt6qN-B8a2pHelLD2fT4x9XyBU7455RxYrx9VqKpifEyio5VhvFPXmPXMTApEjT40KP97x0YFkLIbm9ze8-N6ORI_Lchz78LKP-ISKe32a0eSvKTzvd7bMfWd9iNTlxyeZf9-oxRaWr5GTEWN21VWP6xmWKqj5at5hdzXtUc0R93y_j8vV2cN2bZWn5St8TQyT9ZKlXGx-Ol3oe24N-qdsIH9gLGYxqz3Voif1tPKu2Kv1x33RRL7O-qby1vG7zvpFB-Av8Khrby77Hh6esvrwZ-r8XgG5nErZ-mRRyCKNGKVmYEJEJttEY0qUtdhCaTAUTS0D91sQU2RqCmMf4XUicQKivus926qe0-4wpEIjQg7oqEVNogQJJhBkILRHNKgseClQ9y0xOVk17GNMeEhdyWO7fl5La8c5vHnq67XHYsHf9q_JIcu25IBNvuQjMb5_18zYNMSwUAYRmADPBUFGEW21SjOWRkI489Xg2LHCck7bJAbZvFPCcC_DSI8bvosQfdMFn_FKkhIkKPPaY2BtDGu2zeqauJI_1O0xhtrA7-x8s_ZDfJHq74XD1iu-1sYQ8RW7X6yK1J4PHNKDxys-c3L7sn8A |
linkProvider | Scholars Portal |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Single+Nucleotide+Polymorphisms+in+the+Human+Leukocyte+Antigen+Region+Are+Associated+With+Hemagglutination+Inhibition+Antibody+Response+to+Influenza+Vaccine&rft.jtitle=Frontiers+in+genetics&rft.au=Shuyi+Zhong&rft.au=Hejiang+Wei&rft.au=Mao+Li&rft.au=Yanhui+Cheng&rft.date=2022-02-07&rft.pub=Frontiers+Media+S.A&rft.eissn=1664-8021&rft.volume=13&rft_id=info:doi/10.3389%2Ffgene.2022.790914&rft.externalDBID=DOA&rft.externalDocID=oai_doaj_org_article_09b47aaa1f0a4047a3d195e8bc4642e2 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1664-8021&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1664-8021&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1664-8021&client=summon |