Collins, F. M. Cellular antimicrobial immunity. CRC Crit. Rev. Microbiol. 7, 27–91 (1978).
Mackaness, G. B. Resistance to intracellular infection. J. Infect. Dis. 123, 439–445 (1971).
Albrecht, M. & Arck, P. C. Vertically transferred immunity in neonates: mothers, mechanisms and mediators. Front. Immunol. 11, 555 (2020).
Robbins, J. R. & Bakardjiev, A. I. Pathogens and the placental fortress. Curr. Opin. Microbiol. 15, 36–43 (2012).
Surolia, I. et al. Functionally defective germline variants of sialic acid acetylesterase in autoimmunity. Nature 466, 243–247 (2010).
Clark, E. A. & Giltiay, N. V. CD22: a regulator of innate and adaptive B Cell responses and autoimmunity. Front. Immunol. 9, 2235 (2018).
Mahajan, V. S. & Pillai, S. Sialic acids and autoimmune disease. Immunol. Rev. 269, 145–161 (2016).
Kollmann, T. R., Marchant, A. & Way, S. S. Vaccination strategies to enhance immunity in neonates. Science 368, 612–615 (2020).
Chávez-Arroyo, A. & Portnoy, D. A. Why is Listeria monocytogenes such a potent inducer of CD8+ T-cells? Cell Microbiol. 22, e13175 (2020).
Radoshevich, L. & Cossart, P. Listeria monocytogenes: towards a complete picture of its physiology and pathogenesis. Nat. Rev. Microbiol. 16, 32–46 (2018).
Marchant, A. et al. Maternal immunisation: collaborating with mother nature. Lancet Infect. Dis. 17, e197–e208 (2017).
Fouda, G. G., Martinez, D. R., Swamy, G. K. & Permar, S. R. The Impact of IgG transplacental transfer on early life immunity. Immunohorizons 2, 14–25 (2018).
Kaufmann, S. H., Hug, E. & De Libero, G. Listeria monocytogenes-reactive T lymphocyte clones with cytolytic activity against infected target cells. J. Exp. Med. 164, 363–368 (1986).
Bishop, D. K. & Hinrichs, D. J. Adoptive transfer of immunity to Listeria monocytogenes. The influence of in vitro stimulation on lymphocyte subset requirements. J Immunol. 139, 2005–2009 (1987).
Mielke, M. E., Ehlers, S. & Hahn, H. T-cell subsets in delayed-type hypersensitivity, protection, and granuloma formation in primary and secondary Listeria infection in mice: superior role of Lyt-2+ cells in acquired immunity. Infect. Immun. 56, 1920–1925 (1988).
Bruhns, P. & Jönsson, F. Mouse and human FcR effector functions. Immunol. Rev. 268, 25–51 (2015).
Anthony, R. M., Wermeling, F. & Ravetch, J. V. Novel roles for the IgG Fc glycan. Ann. N. Y. Acad. Sci. 1253, 170–180 (2012).
van de Bovenkamp, F. S., Hafkenscheid, L., Rispens, T. & Rombouts, Y. The emerging importance of IgG Fab glycosylation in immunity. J. Immunol. 196, 1435–1441 (2016).
Traving, C. & Schauer, R. Structure, function and metabolism of sialic acids. Cell. Mol. Life Sci. 54, 1330–1349 (1998).
Langereis, M. A. et al. Complexity and diversity of the mammalian sialome revealed by nidovirus virolectins. Cell Rep. 11, 1966–1978 (2015).
Srivastava, S. et al. Development and applications of sialoglycan-recognizing probes (SGRPs) with defined specificities: exploring the dynamic mammalian sialoglycome. Preprint at bioRxiv https://doi.org/10.1101/2021.05.28.446202 (2021).
Ravindranath, M. H., Higa, H. H., Cooper, E. L. & Paulson, J. C. Purification and characterization of an O-acetylsialic acid-specific lectin from a marine crab Cancer antennarius. J. Biol. Chem. 260, 8850–8856 (1985).
Crocker, P. R., Paulson, J. C. & Varki, A. Siglecs and their roles in the immune system. Nat. Rev. Immunol. 7, 255–266 (2007).
Krištić, J. et al. Profiling and genetic control of the murine immunoglobulin G glycome. Nat. Chem. Biol. 14, 516–524 (2018).
Tsai, S. et al. Transcriptional profiling of human placentas from pregnancies complicated by preeclampsia reveals disregulation of sialic acid acetylesterase and immune signalling pathways. Placenta 32, 175–182 (2011).
Medzihradszky, K. F., Kaasik, K. & Chalkley, R. J. Characterizing sialic acid variants at the glycopeptide level. Anal. Chem. 87, 3064–3071 (2015).
Melo-Braga, M. N., Carvalho, M. B., Emiliano, M. C., Ferreira & Felicori, L. F. New insights of glycosylation role on variable domain of antibody structures. Preprint at bioRxiv https://doi.org/10.1101/2021.04.11.439351 (2021).
Sjoberg, E. R., Powell, L. D., Klein, A. & Varki, A. Natural ligands of the B cell adhesion molecule CD22 beta can be masked by 9-O-acetylation of sialic acids. J. Cell Biol. 126, 549–562 (1994).
Blixt, O., Collins, B. E., van den Nieuwenhof, I. M., Crocker, P. R. & Paulson, J. C. Sialoside specificity of the siglec family assessed using novel multivalent probes: identification of potent inhibitors of myelin-associated glycoprotein. J. Biol. Chem. 278, 31007–31019 (2003).
Brinkman-Van der Linden, E. C. et al. Loss of N-glycolylneuraminic acid in human evolution. Implications for sialic acid recognition by siglecs. J. Biol. Chem. 275, 8633–8640 (2000).
Tedder, T. F. B10 cells: a functionally defined regulatory B cell subset. J. Immunol. 194, 1395–1401 (2015).
Yanaba, K. et al. A regulatory B cell subset with a unique CD1dhiCD5+ phenotype controls T cell-dependent inflammatory responses. Immunity 28, 639–650 (2008).
Horikawa, M. et al. Regulatory B cell (B10 Cell) expansion during Listeria infection governs innate and cellular immune responses in mice. J. Immunol. 190, 1158–1168 (2013).
Lee, C. C. & Kung, J. T. Marginal zone B cell is a major source of Il-10 in Listeria monocytogenes susceptibility. J. Immunol. 189, 3319–3327 (2012).
Liu, D. et al. IL-10-dependent crosstalk between murine marginal zone B cells, macrophages, and CD8α. Immunity 51, 64–76 (2019).
Torres, D. et al. Toll-like receptor 2 is required for optimal control of Listeria monocytogenes infection. Infect. Immun. 72, 2131–2139 (2004).
Edelson, B. T., Cossart, P. & Unanue, E. R. Cutting edge: paradigm revisited: antibody provides resistance to Listeria infection. J. Immunol. 163, 4087–4090 (1999).
Séïté, J. F. et al. IVIg modulates BCR signaling through CD22 and promotes apoptosis in mature human B lymphocytes. Blood 116, 1698–1704 (2010).
Adachi, T. et al. CD22 serves as a receptor for soluble IgM. Eur. J. Immunol. 42, 241–247 (2012).
Müller, J. et al. CD22 ligand-binding and signaling domains reciprocally regulate B-cell Ca2+ signaling. Proc. Natl Acad. Sci. USA 110, 12402–12407 (2013).
Kawasaki, N., Rademacher, C. & Paulson, J. C. CD22 regulates adaptive and innate immune responses of B cells. J. Innate Immun. 3, 411–419 (2011).
Casadevall, A. Antibody-based vaccine strategies against intracellular pathogens. Curr. Opin. Immunol. 53, 74–80 (2018).
Hatta, Y. et al. Identification of the gene variations in human CD22. Immunogenetics 49, 280–286 (1999).
Hunter, C. D. et al. Human neuraminidase isoenzymes show variable activities for 9-O-acetyl-sialoside substrates. ACS Chem. Biol. 13, 922–932 (2018).
Varki, A., Hooshmand, F., Diaz, S., Varki, N. M. & Hedrick, S. M. Developmental abnormalities in transgenic mice expressing a sialic acid-specific 9-O-acetylesterase. Cell 65, 65–74 (1991).
Rizzuto, G. et al. Establishment of fetomaternal tolerance through glycan-mediated B cell suppression. Nature 603, 497–502 (2022).
Fowler, K. B. et al. The outcome of congenital cytomegalovirus infection in relation to maternal antibody status. N. Engl. J. Med. 326, 663–667 (1992).
Boppana, S. B., Rivera, L. B., Fowler, K. B., Mach, M. & Britt, W. J. Intrauterine transmission of cytomegalovirus to infants of women with preconceptional immunity. N. Engl. J. Med. 344, 1366–1371 (2001).
Brown, Z. A. et al. Effect of serologic status and cesarean delivery on transmission rates of herpes simplex virus from mother to infant. JAMA 289, 203–209 (2003).
Hafner, L. et al. Listeria monocytogenes faecal carriage is common and depends on the gut microbiota. Nat. Commun. 12, 6826 (2021).
Hennet, T., Chui, D., Paulson, J. C. & Marth, J. D. Immune regulation by the ST6Gal sialyltransferase. Proc. Natl Acad. Sci. USA 95, 4504–4509 (1998).
Haeussler, M. et al. Evaluation of off-target and on-target scoring algorithms and integration into the guide RNA selection tool CRISPOR. Genome Biol. 17, 148 (2016).
Way, S. S., Kollmann, T. R., Hajjar, A. M. & Wilson, C. B. Cutting edge: protective cell-mediated immunity to Listeria monocytogenes in the absence of myeloid differentiation factor 88. J. Immunol. 171, 533–537 (2003).
Elahi, S. et al. Immunosuppressive CD71+ erythroid cells compromise neonatal host defence against infection. Nature 504, 158–162 (2013).
Shao, T. Y. et al. Commensal Candida albicans positively calibrates systemic Th17 immunological responses. Cell Host Microbe 25, 404–417 (2019).
Turner, L. H. et al. Preconceptual Zika virus asymptomatic infection protects against secondary prenatal infection. PLoS Pathog. 13, e1006684 (2017).
Wasik, B. R. et al. Distribution of O-acetylated sialic acids among target host tissues for influenza virus. mSphere 2, e00379-16 (2017).