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Journal articles on the topic 'Marginal Zone B Cells'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Pillai, Shiv, Annaiah Cariappa, and Stewart T. Moran. "MARGINAL ZONE B CELLS." Annual Review of Immunology 23, no. 1 (2005): 161–96. http://dx.doi.org/10.1146/annurev.immunol.23.021704.115728.

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2

Martin, Flavius, and John F. Kearney. "Marginal-zone B cells." Nature Reviews Immunology 2, no. 5 (2002): 323–35. http://dx.doi.org/10.1038/nri799.

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3

Spencer, Jo, Marta E. Perry, and Deborah K. Dunn-Walters. "Human marginal-zone B cells." Immunology Today 19, no. 9 (1998): 421–26. http://dx.doi.org/10.1016/s0167-5699(98)01308-5.

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4

Weill, Jean-Claude, Sandra Weller, and Claude-Agnès Reynaud. "Human Marginal Zone B Cells." Annual Review of Immunology 27, no. 1 (2009): 267–85. http://dx.doi.org/10.1146/annurev.immunol.021908.132607.

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5

You, Yuying, Riley C. Myers, Larry Freeberg, et al. "Marginal Zone B Cells Regulate Antigen Capture by Marginal Zone Macrophages." Journal of Immunology 186, no. 4 (2011): 2172–81. http://dx.doi.org/10.4049/jimmunol.1002106.

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6

Kleinau, Sandra. "Self-reactive marginal zone B cells." L’annuaire du Collège de France, no. 116 (June 15, 2018): 680. http://dx.doi.org/10.4000/annuaire-cdf.13595.

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7

Hendricks, Jacobus, Nicolaas A. Bos, and Frans G. M. Kroese. "Heterogeneity of Memory Marginal Zone B Cells." Critical Reviews in Immunology 38, no. 2 (2018): 145–58. http://dx.doi.org/10.1615/critrevimmunol.2018024985.

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8

Beck-Engeser, Gabriele B., Rebecca Winkelmann, Matthew L. Wheeler, et al. "APOBEC3 enzymes restrict marginal zone B cells." European Journal of Immunology 45, no. 3 (2015): 695–704. http://dx.doi.org/10.1002/eji.201445218.

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9

Birjandi, Shirin Z., Jill A. Ippolito, Anand K. Ramadorai, and Pamela L. Witte. "Alterations in Marginal Zone Macrophages and Marginal Zone B Cells in Old Mice." Journal of Immunology 186, no. 6 (2011): 3441–51. http://dx.doi.org/10.4049/jimmunol.1001271.

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10

Muppidi, Jagan R., Tal I. Arnon, Yelena Bronevetsky, et al. "Cannabinoid receptor 2 positions and retains marginal zone B cells within the splenic marginal zone." Journal of Experimental Medicine 208, no. 10 (2011): 1941–48. http://dx.doi.org/10.1084/jem.20111083.

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Specialized B cells residing in the splenic marginal zone (MZ) continuously survey the blood for antigens and are important for immunity to systemic infections. However, the cues that uniquely attract cells to the MZ have not been defined. Previous work demonstrated that mice deficient in cannabinoid receptor 2 (CB2) have decreased numbers of MZ B cells but it has been unclear whether CB2 regulates MZ B cell development or positioning. We show that MZ B cells are highly responsive to the CB2 ligand 2-arachidonylglycerol (2-AG) and that CB2 antagonism rapidly displaces small numbers of MZ B cel

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11

Kurtin, Paul J. "Marginal Zone B Cells, Monocytoid B Cells, and the Follicular Microenvironment." American Journal of Clinical Pathology 114, no. 4 (2000): 505–8. http://dx.doi.org/10.1309/l69g-f64h-4f3j-l2r5.

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12

Srivastava, Bhaskar, William J. Quinn, Kristin Hazard, Jan Erikson, and David Allman. "Characterization of marginal zone B cell precursors." Journal of Experimental Medicine 202, no. 9 (2005): 1225–34. http://dx.doi.org/10.1084/jem.20051038.

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Selection of recently formed B cells into the follicular or marginal zone (MZ) compartments is proposed to occur by way of proliferative intermediates expressing high levels of CD21/35 and CD23. However, we show that CD21/35high CD23+ splenocytes are not enriched for proliferative cells, and do not contribute substantially to the generation of follicular B cells. Instead, ontogenic relationships, steady-state labeling kinetics, and adoptive transfer experiments suggest that CD21/35high CD23+ splenocytes serve primarily as precursors for MZ B cells, although their developmental potential seems

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13

Tierens, Anne, Jan Delabie, Lieve Michiels, Peter Vandenberghe, and Chris De Wolf-Peeters. "Marginal-Zone B Cells in the Human Lymph Node and Spleen Show Somatic Hypermutations and Display Clonal Expansion." Blood 93, no. 1 (1999): 226–34. http://dx.doi.org/10.1182/blood.v93.1.226.

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Abstract Splenic marginal-zone B cells, marginal-zone B cells of Peyer’s patches in the gut, and nodal marginal-zone B cells (also identified as monocytoid B cells) share a similar morphology and immunophenotype. These cells likely represent a distinct subset of B cells in humans and rodents, but their precise ontogenetic relationship as well as their origin from B cells of the germinal center is still debated. To study this, we performed a mutation analysis of the rearranged immunoglobulin variable genes (VH) of microdissected single nodal and splenic marginal-zone cells. In addition, we inve

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14

Tierens, Anne, Jan Delabie, Lieve Michiels, Peter Vandenberghe, and Chris De Wolf-Peeters. "Marginal-Zone B Cells in the Human Lymph Node and Spleen Show Somatic Hypermutations and Display Clonal Expansion." Blood 93, no. 1 (1999): 226–34. http://dx.doi.org/10.1182/blood.v93.1.226.401a30_226_234.

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Splenic marginal-zone B cells, marginal-zone B cells of Peyer’s patches in the gut, and nodal marginal-zone B cells (also identified as monocytoid B cells) share a similar morphology and immunophenotype. These cells likely represent a distinct subset of B cells in humans and rodents, but their precise ontogenetic relationship as well as their origin from B cells of the germinal center is still debated. To study this, we performed a mutation analysis of the rearranged immunoglobulin variable genes (VH) of microdissected single nodal and splenic marginal-zone cells. In addition, we investigated

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15

Doyon-Laliberté, Kim, Josiane Chagnon-Choquet, Michelle Byrns, et al. "NR4A Expression by Human Marginal Zone B-Cells." Antibodies 8, no. 4 (2019): 50. http://dx.doi.org/10.3390/antib8040050.

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We have previously characterized a human blood CD19+CD1c+IgM+CD27+CD21loCD10+ innate-like B-cell population, which presents features shared by both transitional immature and marginal zone (MZ) B-cells, named herein “precursor-like” MZ B-cells. B-cells with similar attributes have been associated with regulatory potential (Breg). In order to clarify this issue and better characterize this population, we have proceeded to RNA-Seq transcriptome profiling of mature MZ and precursor-like MZ B-cells taken from the blood of healthy donors. We report that ex vivo mature MZ and precursor-like MZ B-cell

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16

Lopes-Carvalho, Thiago, and John F. Kearney. "Development and selection of marginal zone B cells." Immunological Reviews 197, no. 1 (2004): 192–205. http://dx.doi.org/10.1111/j.0105-2896.2004.0112.x.

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17

DeFranco, Anthony L. "Innate B cells cleave to the marginal zone." Nature Immunology 18, no. 3 (2017): 248–50. http://dx.doi.org/10.1038/ni.3685.

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18

Nus, M., M. Galán, L. Cros-Brunso, et al. "NR4A1 in marginal zone B cells decreases atherosclerosis." Atherosclerosis 315 (December 2020): e91-e92. http://dx.doi.org/10.1016/j.atherosclerosis.2020.10.282.

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19

Singh, Ram, and Jun-Qi Yang. "OR.12. NKT Cells Suppress Autoreactive Marginal Zone B-Cells." Clinical Immunology 119 (January 2006): S8. http://dx.doi.org/10.1016/j.clim.2006.04.014.

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20

Yazbeck, Victor, Ian McConnell, Emily Harris, et al. "Modeling Marginal Zone Lymphomagenesis." Blood 136, Supplement 1 (2020): 31. http://dx.doi.org/10.1182/blood-2020-142768.

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Introduction: Indolent B-Cell Non-Hodgkin's Lymphomas (NHL) represent a heterogeneous group of lymphoproliferative malignancies, that remain largely incurable. Marginal zone lymphomas (MZL) are the second most common subtype of indolent NHL, and lack a unique cytogenetic identifying abnormality. The B-cell receptor signaling pathway is activated in B-cell malignancy and mediates its activity mainly through the Phosphoinositide 3-kinase (PI3K) pathway. Furthermore, novel PI3K inhibitors, such as copanlisib and parsaclisib, have shown impressive clinical activity in several indolent lymphomas in

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21

OGITA, Azusa, Mikako AOKI, Seiji KAWANA, Masami MORIYAMA, Mitsuyoshi HONDA, and Eiichi ARAI. "Two cases of primary cutaneous marginal zone B-cell lymphoma." Skin Cancer 21, no. 3 (2006): 345–49. http://dx.doi.org/10.5227/skincancer.21.345.

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22

Tierens, A., J. Delabie, S. Pittaluga, A. Driessen, and C. DeWolf-Peeters. "Mutation Analysis of the Rearranged Immunoglobulin Heavy Chain Genes of Marginal Zone Cell Lymphomas Indicates an Origin From Different Marginal Zone B Lymphocyte Subsets." Blood 91, no. 7 (1998): 2381–86. http://dx.doi.org/10.1182/blood.v91.7.2381.2381_2381_2386.

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Marginal zone cell lymphoma is a recently described entity among the non-Hodgkin's lymphomas. It likely originates from the marginal zone B cells in the spleen and equivalent cells in the lymph node and extranodal tissues. Recent evidence indicates that marginal zone B cells are functionally heterogeneous and may differ with respect to the pattern of somatic hypermutation in their Ig variable genes. To test whether marginal zone lymphomas may originate from different subsets of marginal zone B cells, we performed a sequence and mutation analysis of the rearranged Ig heavy chain (IgH) variable

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23

Radice, Egle, Rafet Ameti, Serena Melgrati, et al. "Marginal Zone Formation Requires ACKR3 Expression on B Cells." Cell Reports 32, no. 5 (2020): 107951. http://dx.doi.org/10.1016/j.celrep.2020.107951.

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24

Lopes-Carvalho, Thiago, Jeremy Foote, and John F. Kearney. "Marginal zone B cells in lymphocyte activation and regulation." Current Opinion in Immunology 17, no. 3 (2005): 244–50. http://dx.doi.org/10.1016/j.coi.2005.04.009.

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25

MacLennan, Ian C. M. "B cells: The follicular dimension of the marginal zone." Immunology & Cell Biology 86, no. 3 (2008): 219–20. http://dx.doi.org/10.1038/icb.2008.2.

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26

Yeramilli, Venkata A., and Katherine L. Knight. "Development of CD27+marginal zone B cells requires GALT." European Journal of Immunology 43, no. 6 (2013): 1484–88. http://dx.doi.org/10.1002/eji.201243205.

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27

Palm, Anna-Karin E., and Sandra Kleinau. "Marginal zone B cells: From housekeeping function to autoimmunity?" Journal of Autoimmunity 119 (May 2021): 102627. http://dx.doi.org/10.1016/j.jaut.2021.102627.

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28

Gatto, Dominique, and Martin F. Bachmann. "Function of Marginal Zone B Cells in Antiviral B-Cell Responses." Critical Reviews in Immunology 25, no. 4 (2005): 331–42. http://dx.doi.org/10.1615/critrevimmunol.v25.i4.50.

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29

YAMASHITA, K., A. SAKAMOTO, Y. OHKUBO, et al. "c- Overexpression in splenic B cells augments development of marginal zone B cells." Molecular Immunology 42, no. 5 (2005): 617–25. http://dx.doi.org/10.1016/j.molimm.2004.09.011.

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30

Du, Ming-Qing, Huai-Zheng Peng, Ahmet Dogan, et al. "Preferential Dissemination of B-Cell Gastric Mucosa-Associated Lymphoid Tissue (MALT) Lymphoma to the Splenic Marginal Zone." Blood 90, no. 10 (1997): 4071–77. http://dx.doi.org/10.1182/blood.v90.10.4071.

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Abstract The tendency for gastric mucosa-associated lymphoid tissue (MALT) lymphoma cells preferentially to localize around reactive B-cell follicles, both in the mucosa and regional lymph nodes, coupled with their immunophenotype, has led to the proposal that the normal cell counterpart of this lymphoma is the marginal zone B cell. In keeping with this proposition, lymphocytes expressing the lymphoma idiotype have been detected in the splenic marginal zone in a single case of gastric MALT lymphoma. To confirm that this truly represented preferential homing of MALT lymphoma to the splenic marg

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31

Tierens, A., J. Delabie, S. Pittaluga, A. Driessen, and C. DeWolf-Peeters. "Mutation Analysis of the Rearranged Immunoglobulin Heavy Chain Genes of Marginal Zone Cell Lymphomas Indicates an Origin From Different Marginal Zone B Lymphocyte Subsets." Blood 91, no. 7 (1998): 2381–86. http://dx.doi.org/10.1182/blood.v91.7.2381.

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Abstract Marginal zone cell lymphoma is a recently described entity among the non-Hodgkin's lymphomas. It likely originates from the marginal zone B cells in the spleen and equivalent cells in the lymph node and extranodal tissues. Recent evidence indicates that marginal zone B cells are functionally heterogeneous and may differ with respect to the pattern of somatic hypermutation in their Ig variable genes. To test whether marginal zone lymphomas may originate from different subsets of marginal zone B cells, we performed a sequence and mutation analysis of the rearranged Ig heavy chain (IgH)

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32

Depowski, Peter L., Harry Dunn, Sheila Purdy, Jeffrey S. Ross, and Tipu Nazeer. "Splenic Marginal Zone Lymphoma." Archives of Pathology & Laboratory Medicine 126, no. 2 (2002): 214–16. http://dx.doi.org/10.5858/2002-126-0214-smzl.

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Abstract Splenic marginal zone lymphoma is a recently described primary splenic lymphoproliferative disorder that mainly affects older individuals. We report the case of a 22-year-old woman with morphologic and immunophenotypic findings consistent with splenic marginal zone lymphoma. This woman is one of the youngest patients ever described with this disease. The patient presented with complaints of left-sided abdominal fullness and was noted to have splenomegaly on physical examination. Laboratory evaluation revealed pancytopenia and a serum M component. The spleen was removed and weighed 155

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33

Zietara, Natalia, Marcin Łyszkiewicz, Andreas Krueger, and Siegfried Weiss. "ICOS-dependent stimulation of NKT cells by marginal zone B cells." European Journal of Immunology 41, no. 11 (2011): 3125–34. http://dx.doi.org/10.1002/eji.201041092.

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34

Kim, DH, HJ Kim, EJ Choi, et al. "Extranodal marginal zone B-cell lymphomas of the bilateral third eyelids in a dog." Veterinární Medicína 62, No. 6 (2017): 351–55. http://dx.doi.org/10.17221/126/2015-vetmed.

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Extranodal marginal zone B-cell type lymphoma of mucosa-associated lymphoid tissue (MALT) in dogs has similar properties to human low-grade B-cell lymphoma. Both are characterised by a relatively low mitotic rate and a slow manifestation of clinical signs. Primary MALT lymphoma of the third eyelid in canines is very rare. In this case report we describe bilateral MALT lymphoma in a 21-month-old miniature poodle. Histological analysis indicated that the masses were mainly composed of lymphoid cells and lymphoepithelial lesions, a typical feature of MALT lymphoma. Immunohistochemical analysis re

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35

Kretschmer, Karsten, Anke Jungebloud, Jana Stopkowicz, Tanja Kleinke, Reinhard Hoffmann, and Siegfried Weiss. "The Selection of Marginal Zone B Cells Differs from That of B-1a Cells." Journal of Immunology 171, no. 12 (2003): 6495–501. http://dx.doi.org/10.4049/jimmunol.171.12.6495.

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36

Crcareva, Aleksandra, Toshiki Saito, Keiki Kumano, Mamiko Sakata-Yanagimoto, Hisamaru Hirai, and Shigeu Chiba. "Notch2 Regulates Macrophage-Related Genes in Marginal Zone B Cells." Blood 104, no. 11 (2004): 4197. http://dx.doi.org/10.1182/blood.v104.11.4197.4197.

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Abstract [Background] While Notch1 plays critical roles in early T cell development, Notch2 is indispensable for B cell development. Conditional inactivation of Notch2 in the hematopoietic compartment leads to loss of the marginal zone B (MZB) cells and defect in the particular fraction of follicular B (FOB) cells characterized as T2 B cells. Because of their position bordering the marginal sinuses and red pulp in the spleen, MZB cells are amongst the first cells that come in contact with blood-borne substances and thus thought to have critical roles in the defense against bacterial pathogens

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37

Dutta, Sulagna, and Pallav Sengupta. "Functions of follicular and marginal zone B cells in pregnancy." Asian Pacific Journal of Reproduction 7, no. 4 (2018): 191. http://dx.doi.org/10.4103/2305-0500.237058.

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38

Gatto, Dominique, Christiane Ruedl, Bernhard Odermatt, and Martin F. Bachmann. "Rapid Response of Marginal Zone B Cells to Viral Particles." Journal of Immunology 173, no. 7 (2004): 4308–16. http://dx.doi.org/10.4049/jimmunol.173.7.4308.

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39

Morente, M., M. A. Piris, J. L. Orradre, C. Rivas, and R. Villuendas. "Human tonsil intraepithelial B cells: a marginal zone-related subpopulation." Journal of Clinical Pathology 45, no. 8 (1992): 668–72. http://dx.doi.org/10.1136/jcp.45.8.668.

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40

Dammers, Peter M., Nynke K. de Boer, Gerrit Jan Deenen, Paul Nieuwenhuis, and Frans G. M. Kroese. "The origin of marginal zone B cells in the rat." European Journal of Immunology 29, no. 5 (1999): 1522–31. http://dx.doi.org/10.1002/(sici)1521-4141(199905)29:05<1522::aid-immu1522>3.0.co;2-0.

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41

Samardzic, Tatjana, Dragan Marinkovic, Claus-Peter Danzer, Judith Gerlach, Lars Nitschke, and Thomas Wirth. "Reduction of marginal zone B cells in CD22-deficient mice." European Journal of Immunology 32, no. 2 (2002): 561–67. http://dx.doi.org/10.1002/1521-4141(200202)32:2<561::aid-immu561>3.0.co;2-h.

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42

Cinamon, Guy, Marcus A. Zachariah, Olivia M. Lam, Frank W. Foss, and Jason G. Cyster. "Follicular shuttling of marginal zone B cells facilitates antigen transport." Nature Immunology 9, no. 1 (2007): 54–62. http://dx.doi.org/10.1038/ni1542.

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43

Kishi, Y., T. Higuchi, S. Phoon, et al. "Apoptotic marginal zone deletion of anti-Sm/ribonucleoprotein B cells." Proceedings of the National Academy of Sciences 109, no. 20 (2012): 7811–16. http://dx.doi.org/10.1073/pnas.1204509109.

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44

Zandvoort, A., M. E. Lodewijk, N. K. de Boer, P. M. Dammers, F. G. M. Kroese, and W. Timens. "CD27 expression in the human splenic marginal zone: the infant marginal zone is populated by naive B cells." Tissue Antigens 58, no. 4 (2001): 234–42. http://dx.doi.org/10.1034/j.1399-0039.2001.580403.x.

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45

Cariappa, Annaiah, Hsiou-Chi Liou, Bruce H. Horwitz та Shiv Pillai. "Nuclear Factor κb Is Required for the Development of Marginal Zone B Lymphocytes". Journal of Experimental Medicine 192, № 8 (2000): 1175–82. http://dx.doi.org/10.1084/jem.192.8.1175.

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Although immunoglobulin (Ig)MhiIgDlo/−CD21hi marginal zone B cells represent a significant proportion of naive peripheral splenic B lymphocytes, few of the genes that regulate their development have been identified. This subset of peripheral B cells fails to emerge in mice that lack nuclear factor (NF)-κBp50. Less drastic reductions in marginal zone B cell numbers are also seen in the spleens of recombination activating gene (Rag)-2−/− mice reconstituted with NF-κBp65−/− fetal liver cells and in c-Rel−/− mice. In contrast, steady-state levels of IgDhi splenic follicular B cells are not signifi

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46

Samardzic, Tatjana, Dragan Marinkovic, Peter J. Nielsen, Lars Nitschke, and Thomas Wirth. "BOB.1/OBF.1 Deficiency Affects Marginal-Zone B-Cell Compartment." Molecular and Cellular Biology 22, no. 23 (2002): 8320–31. http://dx.doi.org/10.1128/mcb.22.23.8320-8331.2002.

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ABSTRACT Marginal-zone (MZ) B cells represent a first line of defense against particulate blood-borne antigens. Together with the B1 cells, they are responsible for the early response against type II T-independent antigens. The molecular pathways controlling the development of MZ B cells are only poorly understood. We found that these cells are virtually absent in mice deficient in the BOB.1/OBF.1 coactivator. Loss of these B cells was demonstrated by the lack of cells showing the appropriate cell surface phenotype but also by histological analyses and tri-nitro-phenol-Ficoll capturing. The la

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47

Raina, Devisha. "Rare case of gastric extranodal marginal zone lymphoma." International Surgery Journal 8, no. 4 (2021): 1316. http://dx.doi.org/10.18203/2349-2902.isj20210992.

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True histiocytic lymphoma is considered a rare entity, and its diagnosis requires the concordance of morphological, immunophenotypic, and molecular findings. Gastric extra nodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue (MALT) is a B-cell non-Hodgkin lymphoma that arises in the stomach and has a perifollicular/marginal zone growth pattern. The lymphoma is derived from marginal zone B-cells and recapitulates the architecture and organization of native MALT exemplified by the Peyers’ patches in the terminal ileum. Marginal zone lymphoma of MALT (MALT lymphoma) is the mos

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48

Li, Yijin, Hui Li, and Martin Weigert. "Autoreactive B Cells in the Marginal Zone that Express Dual Receptors." Journal of Experimental Medicine 195, no. 2 (2002): 181–88. http://dx.doi.org/10.1084/jem.20011453.

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Allotype and isotype exclusion is a property of most lymphocytes. The reason for this property is not known but it guarantees a high concentration of a single receptor, and threshold numbers of receptors may be required for efficient positive and negative selection. Receptor editing compromises exclusion by sustaining recombination even after a functional receptor is formed. Consequently, B cells expressing multiple receptors arise. We have studied such B cells in which one of the two receptors is anti-self, and find that these partially autoreactive B cells accumulate in the marginal zone. Th

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49

Lee, Hyun Yi, Joong Sun Lee, and Dae Won Koo. "A case report of primary cutaneous marginal zone B-cell lymphoma with mastocytosis." SAGE Open Medical Case Reports 9 (January 2021): 2050313X2110425. http://dx.doi.org/10.1177/2050313x211042527.

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A 53-year-old man presented with asymptomatic, dusky reddish nodules on his trunk, which had persisted for 7 years. Histological findings showed nodular to diffuse dermal infiltration of lymphocytes with irregular nuclei, eosinophils, plasma cells, and mast cells. CD20 revealed patch positivity. Periphery of lymphoid follicles showed BCL-2 positivity and BCL-6 positivity focally at the center. CD30 and toluidine blue staining showed positivity, and several mast cells were confirmed. The immunoglobulin heavy chain gene rearrangement result showed B-cell monoclonality. The patient’s condition wa

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50

Zerra, Patricia E., Seema R. Patel, Connie M. Arthur, Kathryn R. Girard-Pierce, Ashley Bennett, and Sean R. Stowell. "Marginal Zone B Cells Regulate RBC Alloimmunization Toward Distinct RBC Alloantigens." Blood 128, no. 22 (2016): 3847. http://dx.doi.org/10.1182/blood.v128.22.3847.3847.

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Abstract Background: While red blood cell (RBC) transfusion can be beneficial, exposure to allogeneic RBCs can result in the development of RBC alloantibodies that can make it difficult to obtain compatible RBCs for future transfusions. Aside from phenotype matching protocols, no strategy currently exists that is capable of preventing RBC alloimmunization following therapeutic transfusion. As RBC alloantigens represent diverse determinants capable of driving distinct immune pathways, common immunological nodes must be identified in order to successfully prevent RBC alloimmunization against a v

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