Search: onr:"swepub:oai:DiVA.org:uu-396434" > Monoclonal Antibody...
Fältnamn | Indikatorer | Metadata |
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000 | 05427naa a2200505 4500 | |
001 | oai:DiVA.org:uu-396434 | |
003 | SwePub | |
008 | 191106s2019 | |||||||||||000 ||eng| | |
024 | 7 | a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-3964342 URI |
024 | 7 | a https://doi.org/10.1128/JVI.01150-192 DOI |
040 | a (SwePub)uu | |
041 | a engb eng | |
042 | 9 SwePub | |
072 | 7 | a ref2 swepub-contenttype |
072 | 7 | a art2 swepub-publicationtype |
100 | 1 | a Henry, Caroleu Univ Chicago, Dept Med, Sect Rheumatol, 5841 S Maryland Ave, Chicago, IL 60637 USA4 aut |
245 | 1 0 | a Monoclonal Antibody Responses after Recombinant Hemagglutinin Vaccine versus Subunit Inactivated Influenza Virus Vaccine :b a Comparative Study |
264 | 1 | b AMER SOC MICROBIOLOGY,c 2019 |
338 | a print2 rdacarrier | |
520 | a Vaccination is the best measure of protection against influenza virus infection. Vaccine-induced antibody responses target mainly the hemagglutinin (HA) surface glycoprotein, composed of the head and the stalk domains. Recently two novel vaccine platforms have been developed for seasonal influenza vaccination: a recombinant HA vaccine produced in insect cells (Flublok) and Flucelvax, prepared from virions produced in mammalian cells. In order to compare the fine specificity of the antibodies induced by these two novel vaccine platforms, we characterized 42 Flublok-induced monoclonal antibodies (MAbs) and 38 Flucelvax-induced MAbs for avidity, cross-reactivity, and any selectivity toward the head versus the stalk domain. These studies revealed that Flublok induced a greater proportion of MAbs targeting epitopes near the receptor-binding domain on HA head (hemagglutinin inhibition-positive MAbs) than Flucelvax, while the two vaccines induced similar low frequencies of stalk-reactive MAbs. Finally, mice immunized with Flublok and Flucelvax also induced similar frequencies of stalk-reactive antibody-secreting cells, showing that HA head immunodominance is independent of immune memory bias. Collectively, our results suggest that these vaccine formulations are similarly immunogenic but differ in the preferences of the elicited antibodies toward the receptor-binding domain on the HA head.IMPORTANCE: There are ongoing efforts to increase the efficacy of influenza vaccines and to promote production strategies that can rapidly respond to newly emerging viruses. It is important to understand if current alternative seasonal vaccines, such as Flublok and Flucelvax, that use alternate production strategies can induce protective influenza-specific antibodies and to evaluate what type of epitopes are targeted by distinct vaccine formulations. | |
650 | 7 | a MEDICIN OCH HÄLSOVETENSKAPx Medicinska och farmaceutiska grundvetenskaperx Immunologi inom det medicinska området0 (SwePub)301102 hsv//swe |
650 | 7 | a MEDICAL AND HEALTH SCIENCESx Basic Medicinex Immunology in the medical area0 (SwePub)301102 hsv//eng |
650 | 7 | a MEDICIN OCH HÄLSOVETENSKAPx Medicinska och farmaceutiska grundvetenskaperx Mikrobiologi inom det medicinska området0 (SwePub)301092 hsv//swe |
650 | 7 | a MEDICAL AND HEALTH SCIENCESx Basic Medicinex Microbiology in the medical area0 (SwePub)301092 hsv//eng |
653 | a Flublok | |
653 | a Flucelvax | |
653 | a antibody responses | |
653 | a influenza vaccines | |
700 | 1 | a Palm, Anna-Karin E.,d 1983-u Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi,Univ Chicago, Dept Med, Sect Rheumatol, 5841 S Maryland Ave, Chicago, IL 60637 USA4 aut0 (Swepub:uu)annpa506 |
700 | 1 | a Utset, Henry A.u Univ Chicago, Dept Med, Sect Rheumatol, 5841 S Maryland Ave, Chicago, IL 60637 USA4 aut |
700 | 1 | a Huang, Minu Univ Chicago, Dept Med, Sect Rheumatol, 5841 S Maryland Ave, Chicago, IL 60637 USA4 aut |
700 | 1 | a Ho, Irvin Y.u Univ Chicago, Dept Med, Sect Rheumatol, 5841 S Maryland Ave, Chicago, IL 60637 USA4 aut |
700 | 1 | a Zheng, Nai-Yingu Univ Chicago, Dept Med, Sect Rheumatol, 5841 S Maryland Ave, Chicago, IL 60637 USA4 aut |
700 | 1 | a Fitzgerald, Theresau Univ Rochester, Med Ctr, Dept Microbiol & Immunol, Ctr Vaccine Biol & Immunol, Rochester, NY 14642 USA4 aut |
700 | 1 | a Neu, Karlynn E.u Univ Chicago, Dept Med, Sect Rheumatol, 5841 S Maryland Ave, Chicago, IL 60637 USA4 aut |
700 | 1 | a Chen, Yao-Qingu Univ Chicago, Dept Med, Sect Rheumatol, 5841 S Maryland Ave, Chicago, IL 60637 USA4 aut |
700 | 1 | a Krammer, Florianu Icahn Sch Med Mt Sinai, Dept Microbiol, New York, NY 10029 USA4 aut |
700 | 1 | a Treanor, John J.u Univ Rochester, Med Ctr, Dept Med, Div Infect Dis, Rochester, NY 14642 USA4 aut |
700 | 1 | a Sant, Andrea J.u Univ Rochester, Med Ctr, Dept Microbiol & Immunol, Ctr Vaccine Biol & Immunol, Rochester, NY 14642 USA4 aut |
700 | 1 | a Topham, David J.u Univ Rochester, Med Ctr, Dept Microbiol & Immunol, Ctr Vaccine Biol & Immunol, Rochester, NY 14642 USA4 aut |
700 | 1 | a Wilson, Patrick C.u Univ Chicago, Dept Med, Sect Rheumatol, 5841 S Maryland Ave, Chicago, IL 60637 USA4 aut |
710 | 2 | a Univ Chicago, Dept Med, Sect Rheumatol, 5841 S Maryland Ave, Chicago, IL 60637 USAb Institutionen för medicinsk biokemi och mikrobiologi4 org |
773 | 0 | t Journal of Virologyd : AMER SOC MICROBIOLOGYg 93:21q 93:21x 0022-538Xx 1098-5514 |
856 | 4 8 | u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-396434 |
856 | 4 8 | u https://doi.org/10.1128/JVI.01150-19 |
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