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H1N1 challenge results in rapid recall of stem-specific immunity in HA stem nanoparticle–vaccinated newborn monkeys
Kali F. Crofts, Beth C. Holbrook, Courtney L. Page, Maya Sangesland, Masaru Kanekiyo, Martha Alexander-Miller
Kali F. Crofts, Beth C. Holbrook, Courtney L. Page, Maya Sangesland, Masaru Kanekiyo, Martha Alexander-Miller
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Research Article Immunology Infectious disease

H1N1 challenge results in rapid recall of stem-specific immunity in HA stem nanoparticle–vaccinated newborn monkeys

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Abstract

Primary exposure to influenza antigens during infancy shapes the humoral response to subsequent exposures. Development of a universal vaccine approach to protect newborns against influenza would represent a major step forward. In our previous study, we showed vaccination of newborn African green monkeys (AGMs) with an adjuvanted hemagglutinin (HA) stem nanoparticle induced robust IgG responses with broad recognition across HAs. Here, we examined the cellular responses in the lung-draining lymph node of these vaccinated newborn AGMs following challenge with a heterologous H1N1 virus. Our results show that vaccination is associated with early HA stem IgG+ B cell and antibody-secreting cell responses following infection, consistent with a rapidly recalled memory response. In addition, there was evidence of an increase in both HA stem– and head–specific plasma cells in vaccinated animals, suggesting a vaccine-engendered benefit for novel antibodies targeting HA epitopes. Finally, challenge was associated with preferential increases in antibodies that cross-react with H5 HA, suggesting improved protection against this divergent strain. Overall, these findings indicate that HA stem with AddaVax as adjuvant generates a stem-specific cross-reactive memory pool in newborn AGMs with the potential to be rapidly recalled upon infection.

Authors

Kali F. Crofts, Beth C. Holbrook, Courtney L. Page, Maya Sangesland, Masaru Kanekiyo, Martha Alexander-Miller

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Figure 4

H1ssF+AddaVax promotes increases in HA stem– and head–specific PCs in the lung-draining LNs following challenge.

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H1ssF+AddaVax promotes increases in HA stem– and head–specific PCs in th...
(A) Gating strategy to identify PCs (CD20–IgG+CD38+Ki-67–) in the TBLNs on day 7 p.c. (B) Flow cytometric analysis of HA head (H1+H5–) and HA stem (H1+H5+) cells within the PC population for each animal. (C) Percentage of HA head+ and HA stem+ cells within the PC population. (D) Percentage of HA stem+ cells within the total H1+ PC population. (E) Ratio of stem PCs/106 cells to stem PBs/106 cells. (F) Pearson’s correlation analysis using the percentage of HA stem+ PCs in the TBLNs and nAb in the plasma on day 7 p.c. in H1ssF+AddaVax animals. The nAb titers were previously reported in Crofts et al. (24). (G) Pearson’s correlation analysis of the percentage of HA stem+ PCs and percentage of IFN-γ+stem+ Tfh cells in the TBLNs on day 7 p.c. in H1ssF+AddaVax animals. (H) The MFI of H1 probe binding in stem- and head-specific PCs in the TBLNs of H1ssF+AddaVax animals. (I) Ratio of H1 probe binding to IgG in PCs. Ctrl (PBS/Luc mRNA black symbols and H1ssF blue symbols, n = 9), H1ssF+AddaVax (red symbols, n = 8). Data in C represent the median. Statistical significance was determined using a 2-way ANOVA with an uncorrected Fisher’s LSD test (C) or a 2-tailed Mann-Whitney test (D, E, H, and I). The first 5 panels in A are the same as in Figure 1B. *P < 0.05, **P < 0.01, ***P ≤ 0.0005, ****P ≤ 0.0001. nAb data were previously published in Crofts et al. (24) and are shown here in alignment with author reuse policies of the publisher.

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