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Longitudinal dynamics of the human B cell response to the yellow fever 17D vaccine

Wec, Anna Z. (author)
Haslwanter, Denise (author)
Abdiche, Yasmina N. (author)
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Shehata, Laila (author)
Pedreno-Lopez, Nuria (author)
Moyer, Crystal L. (author)
Bornholdt, Zachary A. (author)
Lilov, Asparouh (author)
Nett, Juergen H. (author)
Jangra, Rohit K. (author)
Brown, Michael (author)
Watkins, David I. (author)
Ahlm, Clas, 1956- (author)
Umeå universitet,Institutionen för klinisk mikrobiologi,Clas Ahlm
Forsell, Mattias N. E. (author)
Umeå universitet,Institutionen för klinisk mikrobiologi,Mattias Forsell
Rey, Felix A. (author)
Barba-Spaeth, Giovanna (author)
Chandran, Kartik (author)
Walker, Laura M. (author)
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 (creator_code:org_t)
2020-03-09
2020
English.
In: Proceedings of the National Academy of Sciences of the United States of America. - Washington : National Academy of Science. - 0027-8424 .- 1091-6490. ; 117:12, s. 6675-6685
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • A comprehensive understanding of the development and evolution of human B cell responses duced by pathogen exposure will facilitate the design of next-generation vaccines. Here, we utilized a gh-throughput single B cell cloning technology to longitudinally track the human B cell response to the llow fever virus 17D (YFV-17D) vaccine. The earlymemory B cell (MBC) response was mediated by both assical immunoglobulin M (IgM) (IgM(+)CD27(+)) and switched immunoglobulin (swIg(+)) MBC pulations; however, classical IgM MBCs waned rapidly, whereas swIg(+) and atypical IgM(+) and IgD(+) MBCs were stable over time. Affinity maturation continued for 6 to 9 mo following vaccination, providing evidence for the persistence of germinal center activity long after the period of active viral replication in peripheral blood. Finally, a substantial fraction of the neutralizing antibody response was mediated by public clones that recognize a fusion loop-proximal antigenic site within domain II of the viral envelope glycoprotein. Overall, our findings provide a framework for understanding the dynamics and complexity of human B cell responses elicited by infection and vaccination.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Infektionsmedicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Infectious Medicine (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)

Keyword

antiviral vaccination
antibody responses
yellow fever virus
monoclonal antibody
B cell memory

Publication and Content Type

ref (subject category)
art (subject category)

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