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Life course exposures continually shape antibody profiles and risk of seroconversion to influenza

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Life course exposures continually shape antibody profiles and risk of seroconversion to influenza. / Yang, Bingyi; Lessler, Justin; Zhu, Huachen et al.
In: PLoS Pathogens, Vol. 16, No. 7, e1008635, 23.07.2020.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Yang, B, Lessler, J, Zhu, H, Jiang, CQ, Read, JM, Hay, JA, Kwok, KO, Shen, R, Guan, Y, Riley, S & Cummings, DAT 2020, 'Life course exposures continually shape antibody profiles and risk of seroconversion to influenza', PLoS Pathogens, vol. 16, no. 7, e1008635. https://doi.org/10.1371/journal.ppat.1008635

APA

Yang, B., Lessler, J., Zhu, H., Jiang, C. Q., Read, J. M., Hay, J. A., Kwok, K. O., Shen, R., Guan, Y., Riley, S., & Cummings, D. A. T. (2020). Life course exposures continually shape antibody profiles and risk of seroconversion to influenza. PLoS Pathogens, 16(7), Article e1008635. https://doi.org/10.1371/journal.ppat.1008635

Vancouver

Yang B, Lessler J, Zhu H, Jiang CQ, Read JM, Hay JA et al. Life course exposures continually shape antibody profiles and risk of seroconversion to influenza. PLoS Pathogens. 2020 Jul 23;16(7):e1008635. doi: 10.1371/journal.ppat.1008635

Author

Yang, Bingyi ; Lessler, Justin ; Zhu, Huachen et al. / Life course exposures continually shape antibody profiles and risk of seroconversion to influenza. In: PLoS Pathogens. 2020 ; Vol. 16, No. 7.

Bibtex

@article{0ae7d790de9e4c72a55ebff367f96601,
title = "Life course exposures continually shape antibody profiles and risk of seroconversion to influenza",
abstract = "Complex exposure histories and immune mediated interactions between influenza strains contribute to the life course of human immunity to influenza. Antibody profiles can be generated by characterizing immune responses to multiple antigenically variant strains, but how these profiles vary across individuals and determine future responses is unclear. We used hemagglutination inhibition titers from 21 H3N2 strains to construct 777 paired antibody profiles from people aged 2 to 86, and developed novel metrics to capture features of these profiles. Total antibody titer per potential influenza exposure increases in early life, then decreases in middle age. Increased titers to one or more strains were seen in 97.8% of participants during a roughly four-year interval, suggesting widespread influenza exposure. While titer changes were seen to all strains, recently circulating strains exhibited the greatest titer rise. Higher pre-existing, homologous titers at baseline reduced the risk of seroconversion to recent strains. After adjusting for homologous titer, we also found an increased frequency of seroconversion against recent strains among those with higher immunity to older previously exposed strains. Including immunity to previously exposures also improved the deviance explained by the models. Our results suggest that a comprehensive quantitative description of immunity encompassing past exposures could lead to improved correlates of risk of influenza infection.",
author = "Bingyi Yang and Justin Lessler and Huachen Zhu and Jiang, {Chao Qiang} and Read, {Jonathan M.} and Hay, {James A} and Kwok, {Kin On} and Ruiyin Shen and Yi Guan and Steven Riley and Cummings, {Derek A T}",
year = "2020",
month = jul,
day = "23",
doi = "10.1371/journal.ppat.1008635",
language = "English",
volume = "16",
journal = "PLoS Pathogens",
issn = "1553-7366",
publisher = "Public Library of Science",
number = "7",

}

RIS

TY - JOUR

T1 - Life course exposures continually shape antibody profiles and risk of seroconversion to influenza

AU - Yang, Bingyi

AU - Lessler, Justin

AU - Zhu, Huachen

AU - Jiang, Chao Qiang

AU - Read, Jonathan M.

AU - Hay, James A

AU - Kwok, Kin On

AU - Shen, Ruiyin

AU - Guan, Yi

AU - Riley, Steven

AU - Cummings, Derek A T

PY - 2020/7/23

Y1 - 2020/7/23

N2 - Complex exposure histories and immune mediated interactions between influenza strains contribute to the life course of human immunity to influenza. Antibody profiles can be generated by characterizing immune responses to multiple antigenically variant strains, but how these profiles vary across individuals and determine future responses is unclear. We used hemagglutination inhibition titers from 21 H3N2 strains to construct 777 paired antibody profiles from people aged 2 to 86, and developed novel metrics to capture features of these profiles. Total antibody titer per potential influenza exposure increases in early life, then decreases in middle age. Increased titers to one or more strains were seen in 97.8% of participants during a roughly four-year interval, suggesting widespread influenza exposure. While titer changes were seen to all strains, recently circulating strains exhibited the greatest titer rise. Higher pre-existing, homologous titers at baseline reduced the risk of seroconversion to recent strains. After adjusting for homologous titer, we also found an increased frequency of seroconversion against recent strains among those with higher immunity to older previously exposed strains. Including immunity to previously exposures also improved the deviance explained by the models. Our results suggest that a comprehensive quantitative description of immunity encompassing past exposures could lead to improved correlates of risk of influenza infection.

AB - Complex exposure histories and immune mediated interactions between influenza strains contribute to the life course of human immunity to influenza. Antibody profiles can be generated by characterizing immune responses to multiple antigenically variant strains, but how these profiles vary across individuals and determine future responses is unclear. We used hemagglutination inhibition titers from 21 H3N2 strains to construct 777 paired antibody profiles from people aged 2 to 86, and developed novel metrics to capture features of these profiles. Total antibody titer per potential influenza exposure increases in early life, then decreases in middle age. Increased titers to one or more strains were seen in 97.8% of participants during a roughly four-year interval, suggesting widespread influenza exposure. While titer changes were seen to all strains, recently circulating strains exhibited the greatest titer rise. Higher pre-existing, homologous titers at baseline reduced the risk of seroconversion to recent strains. After adjusting for homologous titer, we also found an increased frequency of seroconversion against recent strains among those with higher immunity to older previously exposed strains. Including immunity to previously exposures also improved the deviance explained by the models. Our results suggest that a comprehensive quantitative description of immunity encompassing past exposures could lead to improved correlates of risk of influenza infection.

U2 - 10.1371/journal.ppat.1008635

DO - 10.1371/journal.ppat.1008635

M3 - Journal article

C2 - 32702069

VL - 16

JO - PLoS Pathogens

JF - PLoS Pathogens

SN - 1553-7366

IS - 7

M1 - e1008635

ER -