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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 2

H1ssF+AddaVax promotes an IFN-γ–producing Tfh cell response that correlates with GC B cell responses on day 7 p.c.

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H1ssF+AddaVax promotes an IFN-γ–producing Tfh cell response that correla...
(A) Gating strategy to identify HA head– (H1+H5–) and HA stem–specific (H1+H5+) GC B cells (CD20+IgG+BCL-6+) in the TBLNs. LD (live/dead viability dye). (B) Percentage of HA head+ and stem+ cells within the GC population. (C) Gating strategy to identify Tfh cells (CD3+CD4+PD-1hiBCL-6+FoxP3– cells). (D) Percentage of Tfh cells within the live CD3+ population. (E) Percentage of IFN-γ+ cells in the Tfh cell population following stimulation with Ca09 HA or NC99 stem peptide pools. (F and G) Pearson’s correlation was performed using the percentage of HA stem+ GC B cells and the percentage of IFN-γ+ Tfh cells in the TBLNs of H1ssF+AddaVax animals (F) or Ctrl animals (G) on day 7 p.c. Ctrl (PBS/Luc mRNA black symbols and H1ssF blue symbols, n = 9), H1ssF+AddaVax (red symbols, n = 8). Data in B and E represent the median. Statistical significance was determined using a 2-way ANOVA with an uncorrected Fisher’s LSD test (B and E) or a 2-tailed Mann-Whitney test (D). The first 4 panels in A are the same as in Figure 1B. Not significant (NS) P > 0.05, ***P < 0.001.

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