TY - JOUR
T1 - Two-dose priming immunization amplifies humoral immunity by synchronizing vaccine delivery with the germinal center response
AU - Bhagchandani, Sachin H.
AU - Yang, Leerang
AU - Lam, Jonathan H.
AU - Maiorino, Laura
AU - Ben-Akiva, Elana
AU - Rodrigues, Kristen A.
AU - Romanov, Anna
AU - Suh, Heikyung
AU - Aung, Aereas
AU - Wu, Shengwei
AU - Wadhera, Anika
AU - Chakraborty, Arup K.
AU - Irvine, Darrell J.
PY - 2024/9/20
Y1 - 2024/9/20
N2 - Prolonging exposure to subunit vaccines during the primary immune response enhances humoral immunity. Escalating-dose immunization (EDI), administering vaccines every other day in an increasing pattern over 2 weeks, is particularly effective but challenging to implement clinically. Here, using an HIV Env trimer/saponin adjuvant vaccine, we explored simplified EDI regimens and found that a two-shot regimen administering 20% of the vaccine followed by the remaining 80% of the dose 7 days later increased TFH responses 6-fold, antigen-specific germinal center (GC) B cells 10-fold, and serum antibody titers 10-fold compared with bolus immunization. Computational modeling of TFH priming and the GC response suggested that enhanced activation/antigen loading on dendritic cells and increased capture of antigen delivered in the second dose by follicular dendritic cells contribute to these effects, predictions we verified experimentally. These results suggest that a two-shot priming approach can be used to substantially enhance responses to subunit vaccines.
AB - Prolonging exposure to subunit vaccines during the primary immune response enhances humoral immunity. Escalating-dose immunization (EDI), administering vaccines every other day in an increasing pattern over 2 weeks, is particularly effective but challenging to implement clinically. Here, using an HIV Env trimer/saponin adjuvant vaccine, we explored simplified EDI regimens and found that a two-shot regimen administering 20% of the vaccine followed by the remaining 80% of the dose 7 days later increased TFH responses 6-fold, antigen-specific germinal center (GC) B cells 10-fold, and serum antibody titers 10-fold compared with bolus immunization. Computational modeling of TFH priming and the GC response suggested that enhanced activation/antigen loading on dendritic cells and increased capture of antigen delivered in the second dose by follicular dendritic cells contribute to these effects, predictions we verified experimentally. These results suggest that a two-shot priming approach can be used to substantially enhance responses to subunit vaccines.
UR - http://www.scopus.com/inward/record.url?scp=85204513113&partnerID=8YFLogxK
U2 - 10.1126/sciimmunol.adl3755
DO - 10.1126/sciimmunol.adl3755
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C2 - 39303017
AN - SCOPUS:85204513113
SN - 2470-9468
VL - 9
SP - eadl3755
JO - Science immunology
JF - Science immunology
IS - 99
ER -