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Journal articles on the topic 'B cell memory'

Author: Grafiati

Published: 4 June 2021

Last updated: 7 February 2022

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1

Bell, Elaine. "SAPping B-cell memory." Nature Reviews Immunology 3, no. 2 (2003): 93. http://dx.doi.org/10.1038/nri1009.

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2

Lanzavecchia, Antonio, and Federica Sallusto. "Human B cell memory." Current Opinion in Immunology 21, no. 3 (2009): 298–304. http://dx.doi.org/10.1016/j.coi.2009.05.019.

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3

Klinman, Norman. "Introduction: B-cell memory." Seminars in Immunology 9, no. 4 (1997): 217. http://dx.doi.org/10.1006/smim.1997.0074.

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4

Visan, Ioana. "Memory B cell induction." Nature Immunology 22, no. 6 (2021): 672. http://dx.doi.org/10.1038/s41590-021-00952-y.

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5

Defrance, Thierry, Morgan Taillardet, and Laurent Genestier. "T cell-independent B cell memory." Current Opinion in Immunology 23, no. 3 (2011): 330–36. http://dx.doi.org/10.1016/j.coi.2011.03.004.

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6

McHeyzer-Williams, Louise J., Melinda Cool, and Michael G. McHeyzer-Williams. "Antigen-Specific B Cell Memory." Journal of Experimental Medicine 191, no. 7 (2000): 1149–66. http://dx.doi.org/10.1084/jem.191.7.1149.

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The mechanisms that regulate B cell memory and the rapid recall response to antigen remain poorly defined. This study focuses on the rapid expression of B cell memory upon antigen recall in vivo, and the replenishment of quiescent B cell memory that follows. Based on expression of CD138 and B220, we reveal a unique and major subtype of antigen-specific memory B cells (B220−CD138−) that are distinct from antibody-secreting B cells (B220+/−CD138+) and B220+CD138− memory B cells. These nonsecreting somatically mutated B220− memory responders rapidly dominate the splenic response and comprise &amp

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7

Fuchs, Ephraim. "Clues to B–cell memory." Nature Medicine 2, no. 7 (1996): 743–44. http://dx.doi.org/10.1038/nm0796-743.

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8

Heidt, Sebastiaan, and Frans HJ Claas. "Preventing Memory B Cell Formation." Transplantation 100, no. 8 (2016): 1605–6. http://dx.doi.org/10.1097/tp.0000000000001254.

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9

Allan, Sarah. "Basophils boost B-cell memory." Nature Reviews Immunology 8, no. 7 (2008): 491. http://dx.doi.org/10.1038/nri2372.

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10

Hosokawa, Tomohide, Akira Aoike, Masamichi Hosono, Shigehiro Motoi, and Keiichi Kawai. "Studies on B-Cell Memory." Microbiology and Immunology 33, no. 11 (1989): 941–49. http://dx.doi.org/10.1111/j.1348-0421.1989.tb00981.x.

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11

Ghosh, Sujal, Oliver Feyen, Ahmad Fasel Jebran, et al. "Memory B Cell Function in HIV-Infected Children—Decreased Memory B Cells Despite ART." Pediatric Research 66, no. 2 (2009): 185–90. http://dx.doi.org/10.1203/pdr.0b013e3181aa057d.

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12

Welsh, Raymond M., Susan E. Stepp, and Eva Szomolanyi-Tsuda. "B cell memory: Sapping the T cell." Nature Medicine 9, no. 2 (2003): 164–66. http://dx.doi.org/10.1038/nm0203-164.

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13

Feldhahn, Niklas, Ines Schwering, Sanggyu Lee, et al. "Silencing of B Cell Receptor Signals in Human Naive B Cells." Journal of Experimental Medicine 196, no. 10 (2002): 1291–305. http://dx.doi.org/10.1084/jem.20020881.

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To identify changes in the regulation of B cell receptor (BCR) signals during the development of human B cells, we generated genome-wide gene expression profiles using the serial analysis of gene expression (SAGE) technique for CD34+ hematopoietic stem cells (HSCs), pre-B cells, naive, germinal center (GC), and memory B cells. Comparing these SAGE profiles, genes encoding positive regulators of BCR signaling were expressed at consistently lower levels in naive B cells than in all other B cell subsets. Conversely, a large group of inhibitory signaling molecules, mostly belonging to the immunogl

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14

Küppers, Ralf. "Human memory B cells: Memory B cells of a special kind." Immunology & Cell Biology 86, no. 8 (2008): 635–36. http://dx.doi.org/10.1038/icb.2008.59.

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15

Yokochi, T., Y. Kato, T. Sugiyama, et al. "Lipopolysaccharide induces apoptotic cell death of B memory cells and regulates B cell memory in antigen-nonspecific manner." FEMS Immunology & Medical Microbiology 15, no. 1 (1996): 1–8. http://dx.doi.org/10.1111/j.1574-695x.1996.tb00351.x.

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16

RIDDERSTAD, A., and D. M. TARLINTON. "B Cell Memory in xid Mice is Long‐Lived Despite Reduced Memory B Cell Frequency." Scandinavian Journal of Immunology 45, no. 6 (1997): 655–59. http://dx.doi.org/10.1046/j.1365-3083.1997.d01-444.x.

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17

Ackermann, Jochen A., Daniel Radtke, Anna Maurberger, Thomas H. Winkler, and Lars Nitschke. "Grb2 regulates B-cell maturation, B-cell memory responses and inhibits B-cell Ca2+signalling." EMBO Journal 30, no. 8 (2011): 1621–33. http://dx.doi.org/10.1038/emboj.2011.74.

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18

Michie, Colin A., and Irvin A. Lampert. "B cell longevity and immunological memory." Trends in Microbiology 5, no. 5 (1997): 180. http://dx.doi.org/10.1016/s0966-842x(97)85011-1.

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19

McHeyzer‐Williams, Louise J., Laurent P. Malherbe, and Michael G. McHeyzer‐Williams. "Checkpoints in memory B‐cell evolution." Immunological Reviews 211, no. 1 (2006): 255–68. http://dx.doi.org/10.1111/j.0105-2896.2006.00397.x.

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20

Wienholt, Louise. "Recommendations for memory b cell reporting." Pathology 52 (February 2020): S45. http://dx.doi.org/10.1016/j.pathol.2020.01.161.

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21

Good-Jacobson, K. L., and D. M. Tarlinton. "Multiple routes to B-cell memory." International Immunology 24, no. 7 (2012): 403–8. http://dx.doi.org/10.1093/intimm/dxs050.

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22

Agematsu, Kazunaga, Sho Hokibara, Haruo Nagumo, and Atsushi Komiyama. "CD27: a memory B-cell marker." Immunology Today 21, no. 5 (2000): 204–6. http://dx.doi.org/10.1016/s0167-5699(00)01605-4.

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23

Nuñez, Gabriel, David Hockenbery, Timothy J. McDonnell, Craig M. Sorensen, and Stanley J. Korsmeyer. "Bcl-2 maintains B cell memory." Nature 353, no. 6339 (1991): 71–73. http://dx.doi.org/10.1038/353071a0.

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24

McHeyzer-Williams, Louise J., and Michael G. McHeyzer-Williams. "ANTIGEN-SPECIFIC MEMORY B CELL DEVELOPMENT." Annual Review of Immunology 23, no. 1 (2005): 487–513. http://dx.doi.org/10.1146/annurev.immunol.23.021704.115732.

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25

WYKES, M., and M. F. GOOD. "Memory B cell responses and malaria." Parasite Immunology 28, no. 1-2 (2006): 31–34. http://dx.doi.org/10.1111/j.1365-3024.2006.00768.x.

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26

Hu, Zhiliang, Zhenwu Luo, Zhuang Wan, et al. "HIV-associated memory B cell perturbations." Vaccine 33, no. 22 (2015): 2524–29. http://dx.doi.org/10.1016/j.vaccine.2015.04.008.

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27

Railey, M. D., G. RA Ehrhardt, and M. D. Cooper. "ONTOGENY OF MEMORY B CELL SUBPOPULATIONS." Journal of Investigative Medicine 52 (January 2004): S288. http://dx.doi.org/10.1097/00042871-200401001-00726.

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28

Williams, Ifor. "Measles infection prunes B cell memory." Science 366, no. 6466 (2019): 702.15–704. http://dx.doi.org/10.1126/science.366.6466.702-o.

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29

Leavy, Olive. "Sequential evolution of B cell memory." Nature Reviews Immunology 16, no. 2 (2016): 73. http://dx.doi.org/10.1038/nri.2016.15.

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30

Tarlinton, David. "B-cell memory: are subsets necessary?" Nature Reviews Immunology 6, no. 10 (2006): 785–90. http://dx.doi.org/10.1038/nri1938.

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31

McHeyzer-Williams, Michael, Shinji Okitsu, Nathaniel Wang, and Louise McHeyzer-Williams. "Molecular programming of B cell memory." Nature Reviews Immunology 12, no. 1 (2011): 24–34. http://dx.doi.org/10.1038/nri3128.

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32

Reipert, Birgit M. "B-cell memory against factor VIII." Cellular Immunology 301 (March 2016): 49–58. http://dx.doi.org/10.1016/j.cellimm.2016.01.003.

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33

Gray, David, Sigridur Bergthorsdottir, Dominic van Essen, Michelle Wykes, Johanne Poudrier, and Kirsten Siepmann. "Observations on memory B-cell development." Seminars in Immunology 9, no. 4 (1997): 249–54. http://dx.doi.org/10.1006/smim.1997.0077.

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34

Quast, Isaak, and David Tarlinton. "B cell memory: understanding COVID-19." Immunity 54, no. 2 (2021): 205–10. http://dx.doi.org/10.1016/j.immuni.2021.01.014.

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35

Muir, Luke, Paul F. McKay, Velislava N. Petrova, et al. "Optimisation of ex vivo memory B cell expansion/differentiation for interrogation of rare peripheral memory B cell subset responses." Wellcome Open Research 2 (October 5, 2017): 97. http://dx.doi.org/10.12688/wellcomeopenres.11386.1.

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Background:Human memory B cells play a vital role in the long-term protection of the host from pathogenic re-challenge. In recent years the importance of a number of different memory B cell subsets that can be formed in response to vaccination or infection has started to become clear. To study memory B cell responses, cells can be culturedex vivo,allowing for an increase in cell number and activation of these quiescent cells, providing sufficient quantities of each memory subset to enable full investigation of functionality. However, despite numerous papers being published demonstrating bulk m

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36

Muir, Luke, Paul F. McKay, Velislava N. Petrova, et al. "Optimisation of ex vivo memory B cell expansion/differentiation for interrogation of rare peripheral memory B cell subset responses." Wellcome Open Research 2 (January 24, 2018): 97. http://dx.doi.org/10.12688/wellcomeopenres.11386.2.

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Background:Human memory B cells play a vital role in the long-term protection of the host from pathogenic re-challenge. In recent years the importance of a number of different memory B cell subsets that can be formed in response to vaccination or infection has started to become clear. To study memory B cell responses, cells can be culturedex vivo,allowing for an increase in cell number and activation of these quiescent cells, providing sufficient quantities of each memory subset to enable full investigation of functionality. However, despite numerous papers being published demonstrating bulk m

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37

Pordes, Aniko Ginta, Christina Hausl, Peter Allacher, et al. "Requirements for Co-Stimulation in T-Cell Dependent and T-Cell Independent Re-Stimulation of FVIII-Specific Memory B Cells." Blood 112, no. 11 (2008): 238. http://dx.doi.org/10.1182/blood.v112.11.238.238.

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Abstract Memory B cells specific for factor VIII (FVIII) are critical for maintaining FVIII inhibitors in patients with hemophilia A. They are precursors of anti-FVIII antibody-producing plasma cells and are highly efficient antigen-presenting cells for the activation of T cells. The eradication of FVIII-specific memory B cells will be a prerequisite for any successful new approach to induce immune tolerance in patients with FVIII inhibitors. Little is known about the regulation of these cells. Previously we showed that ligands for toll-like receptors (TLR) 7 and 9 are able to re-stimulate FVI

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38

Leitenberg, David, Debra L. Burg, and Thomas L. Feldbush. "Lymphokine-induction of memory B-cell differentiation: Differential stimulation of large virgin and memory B-cell differentiation." Cellular Immunology 114, no. 1 (1988): 83–95. http://dx.doi.org/10.1016/0008-8749(88)90256-0.

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39

Liu, Yong-Jun, and Jacques Banchereau. "Regulation of B-cell commitment to plasma cells or to memory B cells." Seminars in Immunology 9, no. 4 (1997): 235–40. http://dx.doi.org/10.1006/smim.1997.0080.

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40

Novi, Giovanni, Francesca Bovis, Sabrina Fabbri, et al. "Tailoring B cell depletion therapy in MS according to memory B cell monitoring." Neurology - Neuroimmunology Neuroinflammation 7, no. 5 (2020): e845. http://dx.doi.org/10.1212/nxi.0000000000000845.

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ObjectiveWe wanted to evaluate efficacy on inflammatory parameters of rituximab (RTX)-personalized reinfusion scheme using a memory B cell–based treatment regimen.MethodsThis is a prospective, uncontrolled, open-label study including patients with MS treated with RTX in 2 Italian MS units. All patients were treated with RTX induction, followed by maintenance infusion at the dosage of 375 mg/m2, according to memory B cell repopulation (0.05% of peripheral-blood mononuclear cells [PBMCs] for the first 2 years, 0.1% of PBMC for the third year). MS activity was assessed as clinical or MRI activity

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41

Berard, Casamayor-Palleja, Billian, Bella, Mondiere, and Defrance. "Activation sensitizes human memory B cells to B-cell receptor-induced apoptosis." Immunology 98, no. 1 (1999): 47–54. http://dx.doi.org/10.1046/j.1365-2567.1999.00842.x.

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42

Asano, M. S., and R. Ahmed. "CD8 T cell memory in B cell-deficient mice." Journal of Experimental Medicine 183, no. 5 (1996): 2165–74. http://dx.doi.org/10.1084/jem.183.5.2165.

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Antigen presentation by B cells and persistence of antigen-antibody complexes on follicular dendritic cells (FDC) have been implicated in sustaining T cell memory. In this study we have examined the role of B cells and antibody in the generation and maintenance of CD8+ cytotoxic T lymphocyte (CTL) memory. To address this issue we compared CTL responses to lymphocytic choriomeningitis virus (LCMV) in normal (+/+) versus B cell-deficient mice. The CTL response to acute LCMV infection can be broken down into three distinct phases: (a) the initial phase (days 3-8 after infection) of antigen-driven

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43

van Essen, Dominic, Per Dullforce, and David Gray. "Role of B cells in maintaining helper T–cell memory." Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences 355, no. 1395 (2000): 351–55. http://dx.doi.org/10.1098/rstb.2000.0572.

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The cellular interactions involved in maintaining CD4 + T–cell memory have hitherto not been identified. In this report, we have investigated the role played by B cells in this process. We show that that longlasting helper T–cell memory depends on the presence of B cells, but that direct antigen presentation by B cells is not required. These findings provide new insights into the mechanisms which underlie helper T–cell memory. They also suggest that the efficacy of future vaccines will depend critically on the inclusion of B– as well as T–cell epitopes.

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44

Jones, Derek D., Joel R. Wilmore, and David Allman. "Cellular Dynamics of Memory B Cell Populations: IgM+and IgG+Memory B Cells Persist Indefinitely as Quiescent Cells." Journal of Immunology 195, no. 10 (2015): 4753–59. http://dx.doi.org/10.4049/jimmunol.1501365.

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45

McHeyzer-Williams, Michael G., and Rafi Ahmed. "B cell memory and the long-lived plasma cell." Current Opinion in Immunology 11, no. 2 (1999): 172–79. http://dx.doi.org/10.1016/s0952-7915(99)80029-6.

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46

Hausl, Christina, Rafi U. Ahmad, Bernhard Baumgartner, Hans Peter Schwarz, Hartmut Ehrlich, and Birgit M. Reipert. "Single-Cell Analysis of FVIII-Specific Memory B Cells in Murine Hemophilia A." Blood 110, no. 11 (2007): 1157. http://dx.doi.org/10.1182/blood.v110.11.1157.1157.

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Abstract The elimination of FVIII-specific memory B cells is an essential step in the design of new therapeutic strategies for the induction of immune tolerance in hemophilia A with FVIII inhibitors. Using a mouse model of hemophilia A we recently reported that low dose FVIII stimulates the differentiation of FVIII-specific memory B cells into antibody-secreting plasma cells whereas high dose FVIII inhibits this process. The inhibition of memory-B-cell re-stimulation is irreversible and seems to be due to an induction of apoptosis. Further understanding of the complex interactions that lead to

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47

Tokuhisa, T., M. Hatano, S. Okada, T. Fukuda, and I. Kunimasa. "Transcriptional regulation of memory B cell development." Modern Rheumatology 11, no. 1 (2001): 1–5. http://dx.doi.org/10.3109/s101650170035.

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48

Dauner, Joseph Gene, Craig P. Chappell, and Joshy Jacob. "Differential localization of memory B cell subsets." FASEB Journal 22, S2 (2008): 370. http://dx.doi.org/10.1096/fasebj.22.2_supplement.370.

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49

Tsiagbe, Vincent K., Phyliis-Jean Linton, and G. Jeanette Tiiorbecke. "The Path of Memory B-Cell Development." Immunological Reviews 126, no. 1 (1992): 113–41. http://dx.doi.org/10.1111/j.1600-065x.1992.tb00634.x.

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50

Desjardins, Marylin, and Bruce D. Mazer. "B-cell memory and primary immune deficiencies." Current Opinion in Allergy and Clinical Immunology 13, no. 6 (2013): 639–45. http://dx.doi.org/10.1097/aci.0000000000000009.

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