Non-responders to egg grown influenza vaccine seroconvert after booster immunization with MDCK cell grown vaccine
We have investigated whether ‘at risk’ subjects who did not respond serologically during a pre-study vaccination with a commercial egg grown influenza sub-unit vaccine would respond to a subsequent vaccination with either a single dose of MDCK cell grown influenza vaccine or a standard egg grown inf...
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Published in | Vaccine Vol. 21; no. 21; pp. 2743 - 2746 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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Elsevier Ltd
20.06.2003
Elsevier Elsevier Limited |
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Abstract | We have investigated whether ‘at risk’ subjects who did not respond serologically during a pre-study vaccination with a commercial egg grown influenza sub-unit vaccine would respond to a subsequent vaccination with either a single dose of MDCK cell grown influenza vaccine or a standard egg grown influenza vaccine containing the same virus strains. We studied 48 non-responder subjects with a mean age 67.5, range: 34–82 years. In this non-responder group the increased immune response that was detected after boosting with an MDCK cell derived vaccine response was variable and relatively modest, except for the A/Texas strain in the vaccine. The proportion of subjects, with an HI titre of ≥40 (protective antibody titre) increased from 50 to 83% (A/Texas strain), from 13 to 25% (B/Harbin strain) and from 38 to 46% (A/Wuhan strain). In comparison a booster vaccination with egg-derived influenza vaccine resulted in an increase immune response with an HI antibody titre ≥40 for two of the three strains, namely from 17 to 58% for the B/Harbin strain and from 8 to 33% for the A/Wuhan strain. |
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AbstractList | We have investigated whether 'at risk' subjects who did not respond serologically during a pre-study vaccination with a commercial egg grown influenza sub-unit vaccine would respond to a subsequent vaccination with either a single dose of MDCK cell grown influenza vaccine or a standard egg grown influenza vaccine containing the same virus strains. We studied 48 non-responder subjects with a mean age 67.5, range: 34-82 years. In this non-responder group the increased immune response that was detected after boosting with an MDCK cell derived vaccine response was variable and relatively modest, except for the A/Texas strain in the vaccine. The proportion of subjects, with an HI titre of >/=40 (protective antibody titre) increased from 50 to 83% (A/Texas strain), from 13 to 25% (B/Harbin strain) and from 38 to 46% (A/Wuhan strain). In comparison a booster vaccination with egg-derived influenza vaccine resulted in an increase immune response with an HI antibody titre >/=40 for two of the three strains, namely from 17 to 58% for the B/Harbin strain and from 8 to 33% for the A/Wuhan strain. We have investigated whether ‘at risk’ subjects who did not respond serologically during a pre-study vaccination with a commercial egg grown influenza sub-unit vaccine would respond to a subsequent vaccination with either a single dose of MDCK cell grown influenza vaccine or a standard egg grown influenza vaccine containing the same virus strains. We studied 48 non-responder subjects with a mean age 67.5, range: 34–82 years. In this non-responder group the increased immune response that was detected after boosting with an MDCK cell derived vaccine response was variable and relatively modest, except for the A/Texas strain in the vaccine. The proportion of subjects, with an HI titre of ≥40 (protective antibody titre) increased from 50 to 83% (A/Texas strain), from 13 to 25% (B/Harbin strain) and from 38 to 46% (A/Wuhan strain). In comparison a booster vaccination with egg-derived influenza vaccine resulted in an increase immune response with an HI antibody titre ≥40 for two of the three strains, namely from 17 to 58% for the B/Harbin strain and from 8 to 33% for the A/Wuhan strain. We have investigated whether 'at risk' subjects who did not respond serologically during a pre-study vaccination with a commercial egg grown influenza sub-unit vaccine would respond to a subsequent vaccination with either a single dose of MDCK cell grown influenza vaccine or a standard egg grown influenza vaccine containing the same virus strains. We studied 48 non-responder subjects with a mean age 67.5, range: 34-82 years. In this non-responder group the increased immune response that was detected after boosting with an MDCK cell derived vaccine response was variable and relatively modest, except for the A/Texas strain in the vaccine. The proportion of subjects, with an HI titre of >/=40 (protective antibody titre) increased from 50 to 83% (A/Texas strain), from 13 to 25% (B/Harbin strain) and from 38 to 46% (A/Wuhan strain). In comparison a booster vaccination with egg-derived influenza vaccine resulted in an increase immune response with an HI antibody titre >/=40 for two of the three strains, namely from 17 to 58% for the B/Harbin strain and from 8 to 33% for the A/Wuhan strain.We have investigated whether 'at risk' subjects who did not respond serologically during a pre-study vaccination with a commercial egg grown influenza sub-unit vaccine would respond to a subsequent vaccination with either a single dose of MDCK cell grown influenza vaccine or a standard egg grown influenza vaccine containing the same virus strains. We studied 48 non-responder subjects with a mean age 67.5, range: 34-82 years. In this non-responder group the increased immune response that was detected after boosting with an MDCK cell derived vaccine response was variable and relatively modest, except for the A/Texas strain in the vaccine. The proportion of subjects, with an HI titre of >/=40 (protective antibody titre) increased from 50 to 83% (A/Texas strain), from 13 to 25% (B/Harbin strain) and from 38 to 46% (A/Wuhan strain). In comparison a booster vaccination with egg-derived influenza vaccine resulted in an increase immune response with an HI antibody titre >/=40 for two of the three strains, namely from 17 to 58% for the B/Harbin strain and from 8 to 33% for the A/Wuhan strain. |
Author | Fleming, D.M Oxford, John S Lambkin, Robert Palache, A.M Al-Jabri, Ali A |
Author_xml | – sequence: 1 givenname: John S surname: Oxford fullname: Oxford, John S organization: Department of Medical Microbiology and Retroscreen Virology, Queen Mary’s School of Medicine and Dentistry, St Bart’s and the London, 327 Mile End Road, London E1 4NS, UK – sequence: 2 givenname: Ali A surname: Al-Jabri fullname: Al-Jabri, Ali A organization: College of Medicine, Sultan Qaboos University, Muscat, Oman – sequence: 3 givenname: Robert surname: Lambkin fullname: Lambkin, Robert organization: Department of Medical Microbiology and Retroscreen Virology, Queen Mary’s School of Medicine and Dentistry, St Bart’s and the London, 327 Mile End Road, London E1 4NS, UK – sequence: 4 givenname: A.M surname: Palache fullname: Palache, A.M organization: Department of Microbiology and Immunology, Solvay Pharmaceuticals, Weesp, The Netherlands – sequence: 5 givenname: D.M surname: Fleming fullname: Fleming, D.M organization: The Royal College of General Practitioners, Birmingham, UK |
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CitedBy_id | crossref_primary_10_1016_j_vaccine_2020_07_043 crossref_primary_10_1038_srep07648 crossref_primary_10_1080_14760584_2019_1639503 crossref_primary_10_1080_21645515_2015_1016666 crossref_primary_10_1016_j_pupt_2013_05_006 crossref_primary_10_3389_fimmu_2017_00784 crossref_primary_10_1515_BC_2008_051 crossref_primary_10_1016_j_vaccine_2014_05_039 crossref_primary_10_1016_j_jviromet_2011_10_016 crossref_primary_10_1080_21645515_2018_1460297 |
Cites_doi | 10.1016/S0264-410X(97)00301-0 10.1038/303706a0 10.7326/0003-4819-124-7-199604010-00010 10.1017/S0022172400022610 10.1002/eji.1830100515 10.1086/514169 10.1016/0042-6822(87)90040-7 10.1086/338014 10.4049/jimmunol.123.3.1356 10.1001/jama.270.16.1956 10.1111/j.1399-0039.1998.tb03001.x 10.1002/eji.1830110309 |
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Keywords | Cell grown vaccine MDCK Influenza vaccine seroconvert Non-responders Immunization Vaccination Orthomyxoviridae Vaccine Infection Virus Prevention Immunoprophylaxis Influenzavirus A Influenza A virus Viral disease Influenza Influenza A |
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Snippet | We have investigated whether ‘at risk’ subjects who did not respond serologically during a pre-study vaccination with a commercial egg grown influenza sub-unit... We have investigated whether 'at risk' subjects who did not respond serologically during a pre-study vaccination with a commercial egg grown influenza sub-unit... |
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SubjectTerms | Adult Age Aged Aged, 80 and over Animals Antibodies, Viral - immunology Biological and medical sciences Cell culture Cell grown vaccine Cell Line Chick Embryo Dogs Eggs Female Fundamental and applied biological sciences. Psychology Hepatitis Humans Immune response Immunization Immunization, Secondary Influenza Influenza A virus - immunology Influenza B virus - immunology Influenza vaccine seroconvert Influenza Vaccines - administration & dosage Influenza Vaccines - adverse effects Influenza Vaccines - immunology Injections, Intramuscular Male MDCK Microbiology Middle Aged Mortality Non-responders Surveys and Questionnaires Vaccination Vaccines Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies Virology |
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Title | Non-responders to egg grown influenza vaccine seroconvert after booster immunization with MDCK cell grown vaccine |
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