Academic literature on the topic 'B cell memory'

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Journal articles on the topic "B cell memory"

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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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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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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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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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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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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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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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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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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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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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Dissertations / Theses on the topic "B cell memory"

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Bell, Jennifer. "Studies on B cell memory." Thesis, University of Edinburgh, 2001. http://hdl.handle.net/1842/13873.

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Weber, Grace E. "Memory B Cell Dysfunction in Human Malaria." Case Western Reserve University School of Graduate Studies / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=case1512731469728517.

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Morrison, Vicky L. "Innate and cognate roles of B cells in T cell differentiation and memory." Thesis, University of Edinburgh, 2011. http://hdl.handle.net/1842/4873.

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B cells recognise antigens on micro-organisms through their B cell receptor (BCR) and via Toll-like receptors (TLRs), and thus respond in both innate and adaptive manners during the subsequent immune response. Innate recognition through TLRs has the potential to alter the behaviour of whole B cell populations. I show, here, that MyD88-dependent activation of B cells via TLR2 or TLR9 causes the rapid loss of expression of CD62L, by metalloproteinasedependent shedding, resulting in the exclusion of these cells from lymph nodes and Peyer’s patches, but not the spleen. Moreover, systemic infection
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Faenzi, Elisa <1981&gt. "Analysis of the memory B cell response against glycoconjugate vaccines." Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2012. http://amsdottorato.unibo.it/4472/.

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The development of vaccines directed against polysaccharide capsules of S. pneumoniae, H. influenzae and N. meningitidis have been of great importance in preventing potentially fatal infections. Bacterial capsular polysaccharides are T-cell-independent antigens that induce specific antibody response characterized by IgM immunoglobulins, with a very low IgG class switched response and lack of capability of inducing a booster response. The inability of pure polysaccharides to induce sustained immune responses has required the development of vaccines containing polysaccharides conjugated to a car
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Murugan, Rajagopal. "Protective memory B cell response in controlled human malaria infection." Doctoral thesis, Humboldt-Universität zu Berlin, 2019. http://dx.doi.org/10.18452/19695.

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Antikörper gegen Circumsporozoite protein (CSP), ein Oberflächenantigen von Plasmodium falciparum (Pf), können sterile Immunität hervorrufen und dadurch die Entwicklung von Malaria im Tierversuch verhindern. Im Menschen werden protektive B-Zell Gedächtnisantworten gegen CSP durch natürliche Malariaerkrankung bzw. Vakzinierung jedoch nur unzureichend erzeugt. - Für die Entwicklung von Gedächtnis-B-Zellen stellt die Affinitätsreifung, welche durch somatische Immungobulin Hypermutation sowie der nachfolgenden Selektion von B-Zellen mit verbesserter Antigenaffinität charakterisiert ist, eine
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Monaghan, Tanya Marie. "Circulating antibody and memory B cell responses to Clostridium difficile toxins A and B." Thesis, University of Nottingham, 2013. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.595681.

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In C. difficile infection (COl), the antibody-mediated immune response to secreted toxins A and B appears to be important in determining the nature of clinical disease. The aim of this study was to evaluate multiple aspects of the humoral immune response to C. difficife toxins A and B in patients with C. difficile-associated disease (COAO), among which included subjects with inflammatory bowel disease. Humoral immune measurements were also quantified for healthy controls and patients with cystic fibrosis (CF) who have been reported to rarely develop COl. Isolated peripheral blood mononuclear c
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Trück, Johannes. "B cell response to pneumococcal vaccines." Thesis, University of Oxford, 2014. http://ora.ox.ac.uk/objects/uuid:4bbccd8c-febd-4713-a97b-d6a8a08e3979.

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Streptococcus pneumoniae is a significant cause of mortality and morbidity in both children and older adults, with infection resulting in invasive disease, pneumonia and otitis media. The inclusion of pneumococcal conjugate vaccines in routine infant immunisation programmes has had a major impact on disease rates. Vaccine-induced protection against pneumococcal infection is thought to be mediated by the generation of persistent serotype-specific functional antibodies and antigen-specific memory B cells, the latter capable of generating a rapid secondary antibody response on re-exposure to anti
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Mietzner, Brun Henning. "IgG memory B cell antibodies in patients with systemic lupus erythematosus." Doctoral thesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät I, 2009. http://dx.doi.org/10.18452/16078.

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Die beständige Autoantikörperproduktion in Patienten mit Systemischem Lupus Erythematodes (SLE) suggeriert die Existenz eines autoreaktiven humoralen Gedächtnisses; die Häufigkeit selbstreaktiver Gedächtnis-B-Zellen in SLE wurde jedoch noch nicht ermittelt. Unter normalen Umständen exprimieren neu gebildete B-Zellen im Knochenmark Autoantikörper mit hoher Frequenz, darunter auch antinukleäre Antikörper. Diese autoreaktiven B Zellen unterliegen einer strengen Überwachung an zwei Kontrollpunkten für Selbsttoleranz, einer im Knochenmark und einer in der Peripherie. Im Gegensatz dazu steht SLE mit
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Muhammad, Khalid. "Longterm impact of anti-CD20 mediated transient B cell depletion on memory B cells in patients with rheumatoid arthritis." Doctoral thesis, kostenfrei, 2009. https://nbn-resolving.org/urn:nbn:de:bvb:20-opus-36319.

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B-Lymphozyten leisten unterschiedliche Beiträge zur Pathophysiologie der Rheumatoiden Arthritis. Sie produzieren Autoantikörper, präsentieren Autoantigene und schütten verschiedene Zytokine, die am proinflammatorischen Prozess beteiligt sind, aus. Aufbauend auf diesen Ergebnissen wurden in den letzten Jahren Therapien entwickelt, die gezielt B-Lymphozyten ansteuern um direkt oder indirekt in den autoimmunen Krankheitsverlauf einzugreifen. Die zeitlich begrenzte B-Zell-Depletion mit Rituximab (anti CD20-Antikörper) hat dabei in den letzten Jahren einen hohen Stellenwert erlangt und wird im klin
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Lazarus, Rajeka. "Memory B-cell responses to pneumococcal polysaccharide and conjugate vaccines in adults." Thesis, University of Oxford, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.549609.

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Books on the topic "B cell memory"

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MacCombie, Bruce. Elegy: To the memory of Stephen Albert : for clarinet in B-flat, violin, violoncello, and piano. Helicon Music, 1994.

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Dörner, Thomas, and Peter E. Lipsky. Cellular side of acquired immunity (B cells). Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0050.

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B cells have gained interest in rheumatoid arthritis (RA) beyond being the precursors of antibody-producing plasma cells since they are also a broader component of the adaptive immune system. They are capable of functioning as antigen-presenting cells for T-cell activation and can produce an array of cytokines. Disturbances of peripheral B-cell homeostasis together with the formation of ectopic lymphoid neogenesis within the inflamed synovium appears to be a characteristic of patients with RA. Enhanced generation of memory B cells and autoreactive plasma cells producing IgM-RF and ACPA-IgG ant
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Bunch, Chris. Chronic leukaemia. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0287.

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In the chronic leukaemias, leukaemogenesis occurs in two different cell types (and possibly even two different anatomical sites), leading to two very different forms of the disease: chronic myeloid leukaemia and chronic lymphocytic leukaemia. Chronic myeloid leukaemia is best thought of as a myeloproliferative disorder. It is a clonal disorder of the haematopoietic stem cell, leading to overproduction of the myeloid cells: neutrophils and their precursors, basophils and eosinophils. By contrast, chronic lymphocytic leukaemia can be viewed as a low-grade lymphoma. It is a clonal disorder of mat
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Gray, David. Immunological Memory (Current Topics in Microbiology & Immunology). Edited by David Gray. Springer, 1990.

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(Editor), B. Pulendran, and R. Ahmed (Editor), eds. From Innate Immunity to Immunological Memory (Current Topics in Microbiology and Immunology). Springer, 2006.

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Voll, Reinhard E., and Barbara M. Bröker. Innate vs acquired immunity. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0048.

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The innate and the adaptive immune system efficiently cooperate to protect us from infections. The ancient innate immune system, dating back to the first multicellular organisms, utilizes phagocytic cells, soluble antimicrobial peptides, and the complement system for an immediate line of defence against pathogens. Using a limited number of germline-encoded pattern recognition receptors including the Toll-like, RIG-1-like, and NOD-like receptors, the innate immune system recognizes so-called pathogen-associated molecular patterns (PAMPs). PAMPs are specific for groups of related microorganisms
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Book chapters on the topic "B cell memory"

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MacLennan, I. C. M., Y. J. Liu, S. Oldfield, J. Zhang, and P. J. L. Lane. "The Evolution of B-Cell Clones." In Immunological Memory. Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-75244-5_3.

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McHeyzer-Williams, Louise J., and Michael G. McHeyzer-Williams. "Analysis of Antigen-Specific B-Cell Memory Directly Ex Vivo." In B Cell Protocols. Humana Press, 2004. http://dx.doi.org/10.1385/1-59259-796-3:173.

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Gray, D., and T. Leanderson. "Expansion, Selection and Maintenance of Memory B-Cell Clones." In Immunological Memory. Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-75244-5_1.

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Klinman, N. R., and P. J. Linton. "The Generation of B-Cell Memory: A Working Hypothesis." In Immunological Memory. Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-75244-5_2.

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Berek, Claudia. "B-Cell Maturation and Immunological Memory." In Encyclopedia of Immunotoxicology. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-27786-3_155-5.

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Herzenberg, L. A., and A. Stall. "B Cell Lineages and Immunologic Memory." In Progress in Immunology. Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-83755-5_54.

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Berek, Claudia. "B-Cell Maturation and Immunological Memory." In Encyclopedia of Immunotoxicology. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-54596-2_155.

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Wienands, Jürgen, and Niklas Engels. "The Memory Function of the B Cell Antigen Receptor." In Current Topics in Microbiology and Immunology. Springer International Publishing, 2015. http://dx.doi.org/10.1007/82_2015_480.

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Klinman, N. R. "Repertoire Diversification of Primary vs Memory B Cell Subsets." In Current Topics in Microbiology and Immunology. Springer Berlin Heidelberg, 1998. http://dx.doi.org/10.1007/978-3-642-71984-4_10.

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Oldfield, Susan, Liu Yong-Jun, Martin Beaman, and C. M. MacLennan. "Memory B Cells Generated in T Cell-Dependent Antibody Responses Colonise the Splenic Marginal Zone." In Advances in Experimental Medicine and Biology. Springer US, 1988. http://dx.doi.org/10.1007/978-1-4684-5535-9_13.

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Conference papers on the topic "B cell memory"

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Costa, Leonardo, Jürgen Haas, Henriette Rudolph, et al. "The Choroid Plexus Is Permissive for a Preactivated Antigen-Experienced Memory B Cell Subset in Multiple Sclerosis." In Building Bridges in Medical Science 2021. Cambridge Medicine Journal, 2021. http://dx.doi.org/10.7244/cmj.2021.03.001.2.

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Background: The role of B cells in multiple sclerosis (MS) is increasingly recognized. B cells undergo compartmentalized redistribution in blood and cerebrospinal fluid (CSF) during active MS, whereby memory B cells accumulate in the CSF. While B-cell trafficking across the blood– brain barrier has been intensely investigated, cellular diapedesis through the blood–CSF barrier (BCSFB) is incompletely understood. Objectives: To investigate how B cells interact with the choroid plexus to transmigrate into the CSF, we isolated circulating B cells from healthy donors (HC) and MS patients, utilized
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Breen, M., F. Feng, K. Barker, et al. "Lung Memory B Cell Populations After Influenza Infection in Mice." In American Thoracic Society 2019 International Conference, May 17-22, 2019 - Dallas, TX. American Thoracic Society, 2019. http://dx.doi.org/10.1164/ajrccm-conference.2019.199.1_meetingabstracts.a5903.

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Yoshikawa, Kuniyoshi. "Guide-Lines on Flash Memory Cell Selection." In 1998 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 1998. http://dx.doi.org/10.7567/ssdm.1998.b-3-2.

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Cheng, Bin, Ling-yun Liu, Zhao-hui Qi, and Hong-guang Yang. "Prediction of Continuous B-cell Epitopes Using Long Short Term Memory Networks." In ICBCB 2018: 2018 6th International Conference on Bioinformatics and Computational Biology. ACM, 2018. http://dx.doi.org/10.1145/3194480.3194493.

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Moura, RA, C. Quaresma, AR Vieira, et al. "SAT0170 B-cell phenotype and igd-cd27- memory b cells are affected by tnf-inhibitors and tocilizumab treatment in rheumatoid arthritis." In Annual European Congress of Rheumatology, 14–17 June, 2017. BMJ Publishing Group Ltd and European League Against Rheumatism, 2017. http://dx.doi.org/10.1136/annrheumdis-2017-eular.3011.

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Moura, Rita A., Cláudia Quaresma, Ana R. Vieira, et al. "01.06 B-cell phenotype and igd-cd27- memory b cells are affected by tnf-inhibitors and tocilizumab treatment in rheumatoid arthritis." In 37th European Workshop for Rheumatology Research 2–4 March 2017 Athens, Greece. BMJ Publishing Group Ltd and European League Against Rheumatism, 2017. http://dx.doi.org/10.1136/annrheumdis-2016-211048.6.

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Rao, R. A., R. F. Steimle, M. Sadd, et al. "Hot Carrier Injection/Fowler Nordheim Erase Silicon Nanocrystal Memory Cell." In 2003 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2003. http://dx.doi.org/10.7567/ssdm.2003.b-6-1.

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Kling, Heather, Jan Kristoff, Tim Shipley, Xiuping Shao, Alison Morris, and Karen Norris. "Pneumocystis-specific B-cell Memory Response Protects Against Colonization In SHIV-infected Macaques." In American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a5216.

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Ringheim, GE, J. Kosek, L. Capone, PH Schafer, and Y. Nakayama. "SAT0028 Aiolos overexpression in systemic lupus erythematosus b-cell subtypes and baff induced memory b-cell differentiation are reduced by cc-220 modulation of cereblon activity." In Annual European Congress of Rheumatology, 14–17 June, 2017. BMJ Publishing Group Ltd and European League Against Rheumatism, 2017. http://dx.doi.org/10.1136/annrheumdis-2017-eular.5294.

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Shchukina, Irina A., Ivan I. Tokin, Ivan B. Tokin, and Galina F. Filimonova. "Quantitative evaluation of the cell population structure of the liver biopsy specimens of patients with chronic hepatitis B." In 2015 International Conference "Stability and Control Processes" in Memory of V.I. Zubov (SCP). IEEE, 2015. http://dx.doi.org/10.1109/scp.2015.7342205.

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