Synonyms
CD27+ IgM+ IgD+ B cells; IgM memory B cells
Definition
Marginal zone (MZ) B cells are a subpopulation of B lymphocytes that localize at the border of the red and white pulp in the spleen where they are positioned to sample blood-borne antigens. Accordingly, MZ B cells mount rapid and T cell–independent antibody responses to blood-borne pathogens that display repetitive epitopes such as the polysaccharides found on encapsulated bacteria and viral coat proteins. They are derived as a separate lineage from naïve follicular B cells and express a unique phenotype. The antibodies produced by MZ B cells bear little-to-no mutation but often display polyreactive and auto-reactive specificities.
Introduction
Antibodies are a critical component of adaptive immunity and their production is a cooperative effort between different B cell subpopulations (Swanson et al. 2013). MZ B cells contribute to humoral immunity upon pathogen infection by rapidly producing pathogen-specific antibodies...
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References
Briney BS, Willis JR, McKinney BA, Crowe Jr JE. High-throughput antibody sequencing reveals genetic evidence of global regulation of the naive and memory repertoires that extends across individuals. Genes Immun. 2012;13(6):469–73. doi:10.1038/gene.2012.20.
Capolunghi F, Cascioli S, Giorda E, Rosado MM, Plebani A, Auriti C, et al. CpG drives human transitional B cells to terminal differentiation and production of natural antibodies. J Immunol. 2008;180(2):800–8.
Cerutti A, Cols M, Puga I. Marginal zone B cells: virtues of innate-like antibody-producing lymphocytes. Nat Rev Immunol. 2013;13(2):118–32. doi:10.1038/nri3383.
Chen C, Stenzel-Poore MP, Rittenberg MB. Natural auto- and polyreactive antibodies differing from antigen-induced antibodies in the H chain CDR3. J Immunol. 1991;147(7):2359–67.
Cyster JG, Schwab SR. Sphingosine-1-phosphate and lymphocyte egress from lymphoid organs. Annu Rev Immunol. 2012;30:69–94. doi:10.1146/annurev-immunol-020711-075011.
Gatto D, Bachmann MF. Function of marginal zone B cells in antiviral B-cell responses. Crit Rev Immunol. 2005;25(4):331–42.
Klein U, Rajewsky K, Kuppers R. Human immunoglobulin (Ig)M + IgD + peripheral blood B cells expressing the CD27 cell surface antigen carry somatically mutated variable region genes: CD27 as a general marker for somatically mutated (memory) B cells. J Exp Med. 1998;188(9):1679–89.
Kruetzmann S, Rosado MM, Weber H, Germing U, Tournilhac O, Peter HH, et al. Human immunoglobulin M memory B cells controlling Streptococcus pneumoniae infections are generated in the spleen. J Exp Med. 2003;197(7):939–45. doi:10.1084/jem.20022020.
Martin F, Kearney JF. Marginal-zone B cells. Nat Rev Immunol. 2002;2(5):323–35. doi:10.1038/nri799.
Mebius RE, Kraal G. Structure and function of the spleen. Nat Rev Immunol. 2005;5(8):606–16. doi:10.1038/nri1669.
Pillai S, Cariappa A, Moran ST. Marginal zone B cells. Annu Rev Immunol. 2005;23:161–96. doi:10.1146/annurev.immunol.23.021704.115728.
Schelonka RL, Tanner J, Zhuang Y, Gartland GL, Zemlin M, Schroeder Jr HW. Categorical selection of the antibody repertoire in splenic B cells. Eur J Immunol. 2007;37(4):1010–21. doi:10.1002/eji.200636569.
Snapper CM, Yamada H, Smoot D, Sneed R, Lees A, Mond JJ. Comparative in vitro analysis of proliferation, Ig secretion, and Ig class switching by murine marginal zone and follicular B cells. J Immunol. 1993;150(7):2737–45.
Song H, Cerny J. Functional heterogeneity of marginal zone B cells revealed by their ability to generate both early antibody-forming cells and germinal centers with hypermutation and memory in response to a T-dependent antigen. J Exp Med. 2003;198(12):1923–35. doi:10.1084/jem.20031498.
Steiniger B, Bette M, Schwarzbach H. The open microcirculation in human spleens: a three-dimensional approach. J Histochem Cytochem. 2011;59(6):639–48. doi:10.1369/0022155411408315.
Swanson CL, Pelanda R, Torres RM. Division of labor during primary humoral immunity. Immunol Res. 2013;55((1–3)):277–86. doi:10.1007/s12026-012-8372-9.
Weill JC, Weller S, Reynaud CA. Human marginal zone B cells. Annu Rev Immunol (Rev). 2009;27:267–85. doi:10.1146/annurev.immunol.021908.132607.
Weller S, Braun MC, Tan BK, Rosenwald A, Cordier C, Conley ME, et al. Human blood IgM “memory” B cells are circulating splenic marginal zone B cells harboring a prediversified immunoglobulin repertoire. Blood. 2004;104(12):3647–54. doi:10.1182/blood-2004-01-0346.
Weller S, Bonnet M, Delagreverie H, Israel L, Chrabieh M, Marodi L, et al. IgM + IgD + CD27+ B cells are markedly reduced in IRAK-4-, MyD88-, and TIRAP- but not UNC-93B-deficient patients. Blood. 2012;120(25):4992–5001. doi:10.1182/blood-2012-07-440776.
Zhou J, Lottenbach KR, Barenkamp SJ, Lucas AH, Reason DC. Recurrent variable region gene usage and somatic mutation in the human antibody response to the capsular polysaccharide of Streptococcus pneumoniae type 23 F. Infect Immun. 2002;70(8):4083–91.
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Torres, R.M., Pujanauski, L. (2014). Marginal Zone B Cells. In: Mackay, I.R., Rose, N.R., Diamond, B., Davidson, A. (eds) Encyclopedia of Medical Immunology. Springer, New York, NY. https://doi.org/10.1007/978-0-387-84828-0_560
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