A conserved antigen induces respiratory Th17-mediated serotype-independent protection against pneumococcal superinfection

Abstract

SummarySeveral vaccines targeting bacterial pathogens show reduced efficacy in the context of intercurrent viral infection indicating a new vaccinology approach is required to protect against such superinfections. To find antigens for the human pathogenStreptococcus pneumoniaethat are effective following influenza infection, we performed CRISPRi-seq in a murine model of superinfection and identified the highly conservedlafBgene as virulence factor. We show that LafB is a membrane-associated, intracellular protein that catalyzes the formation of galactosyl-glucosyl-diacylglycerol, a glycolipid we show is important for cell wall homeostasis. Respiratory vaccination with recombinant LafB, in contrast to subcutaneous vaccination, was highly protective against all serotypes in a murine model. In contrast to standard pneumococcal capsule-based conjugate vaccines, protection did not require LafB-specific antibodies but was dependent on airway CD4+T helper 17 cells. Healthy human individuals can elicit LafB-specific immune responses, suggesting its merit as a universal pneumococcal vaccine antigen that remains effective following influenza infection.One-Sentence SummaryDiscovery of a universal pneumococcal vaccine protective during superinfection.