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Critical Reviews™ in Immunology

Publicado 6 números por año

ISSN Imprimir: 1040-8401

ISSN En Línea: 2162-6472

The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two preceding years. 2017 Journal Citation Reports (Clarivate Analytics, 2018) IF: 1.3 To calculate the five year Impact Factor, citations are counted in 2017 to the previous five years and divided by the source items published in the previous five years. 2017 Journal Citation Reports (Clarivate Analytics, 2018) 5-Year IF: 2.6 The Eigenfactor score, developed by Jevin West and Carl Bergstrom at the University of Washington, is a rating of the total importance of a scientific journal. Journals are rated according to the number of incoming citations, with citations from highly ranked journals weighted to make a larger contribution to the eigenfactor than those from poorly ranked journals. Eigenfactor: 0.00079 The Journal Citation Indicator (JCI) is a single measurement of the field-normalized citation impact of journals in the Web of Science Core Collection across disciplines. The key words here are that the metric is normalized and cross-disciplinary. JCI: 0.24 SJR: 0.429 SNIP: 0.287 CiteScore™:: 2.7 H-Index: 81

Indexed in

Heterogeneity of Memory Marginal Zone B Cells

Volumen 38, Edición 2, 2018, pp. 145-158
DOI: 10.1615/CritRevImmunol.2018024985
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SINOPSIS

The marginal zone (MZ) is largely composed of a unique subpopulation of B cells, the so-called MZ-B cells. At a molecular level, memory B cells are characterized by the presence of somatically mutated IGV genes. The earliest studies in the rat have documented the presence of hapten-specific MZ-B cells after immunization in the MZ. This work later received experimental support demonstrating that the IGHV-Cμ transcripts expressed by phenotypically defined splenic MZ-B cells (defined as CD90negIgMhighIgDlow B cells) can carry somatic hypermutation. However, only a minor fraction (< 10%–20%) of these MZ-B cells is mutated and is considered to represent memory B cells. Memory B cells can either be class-switched (IgG, IgA, IgE), or non–class-switched (IgM) B cells. B cells in the MZ are a heterogeneous population of cells and both naïve MZ-B cells; class switched and unswitched memory MZ-B cells are present at this unique site in the spleen. Naïve MZ-B cells carry unmutated Ig genes, produce low-affinity IgM molecules and constitute a first line of defense against invading pathogens. Memory MZ-B cells express high-affinity Ig molecules, directed to (microbial) antigens that have been encountered. In this review, we report on the memory compartment of splenic MZ-B cells in the rat to provide insights into the origin and function of these memory MZ-B cells.

CITADO POR
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  2. Allie S. Rameeza, Randall Troy D., Resident Memory B Cells, Viral Immunology, 33, 4, 2020. Crossref

  3. Colombo Monica, Bagnara Davide, Reverberi Daniele, Matis Serena, Cardillo Martina, Massara Rosanna, Mastracci Luca, Ravetti Jean Louis, Agnelli Luca, Neri Antonino, Mazzocco Michela, Squillario Margherita, Mazzarello Andrea Nicola, Cutrona Giovanna, Agathangelidis Andreas, Stamatopoulos Kostas, Ferrarini Manlio, Fais Franco, Tracing CLL-biased stereotyped immunoglobulin gene rearrangements in normal B cell subsets using a high-throughput immunogenetic approach, Molecular Medicine, 26, 1, 2020. Crossref

  4. Stranavova Lucia, Hruba Petra, Slatinska Janka, Sawitzki Birgit, Reinke Petra, Volk Hans-Dieter, Viklicky Ondrej, Dialysis therapy is associated with peripheral marginal zone B-cell augmentation, Transplant Immunology, 60, 2020. Crossref

  5. Ochocinski Dominik, Dalal Mansi, Black L. Vandy, Carr Silvana, Lew Judy, Sullivan Kevin, Kissoon Niranjan, Life-Threatening Infectious Complications in Sickle Cell Disease: A Concise Narrative Review, Frontiers in Pediatrics, 8, 2020. Crossref

  6. Lyashchenko Konstantin P., Vordermeier H. Martin, Waters W. Ray, Memory B cells and tuberculosis, Veterinary Immunology and Immunopathology, 221, 2020. Crossref

  7. Marinkovic Dragan, Marinkovic Tatjana, Putative role of marginal zone B cells in pathophysiological processes, Scandinavian Journal of Immunology, 92, 3, 2020. Crossref

  8. Palm Anna-Karin E., Kleinau Sandra, Marginal zone B cells: From housekeeping function to autoimmunity?, Journal of Autoimmunity, 119, 2021. Crossref

  9. Perez-Chacon Gema, Zapata Juan M., The Traf2DNxBCL2-tg Mouse Model of Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma Recapitulates the Biased IGHV Gene Usage, Stereotypy, and Antigen-Specific HCDR3 Selection of Its Human Counterpart, Frontiers in Immunology, 12, 2021. Crossref

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  11. Doyon-Laliberté Kim, Aranguren Matheus, Poudrier Johanne, Roger Michel, Marginal Zone B-Cell Populations and Their Regulatory Potential in the Context of HIV and Other Chronic Inflammatory Conditions, International Journal of Molecular Sciences, 23, 6, 2022. Crossref

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  13. Sedimbi Saikiran K., Hägglöf Thomas, Garimella Manasa G., Wang Shan, Duhlin Amanda, Coelho Ana, Ingelshed Katrine, Mondoc Emma, Malin Stephen G., Holmdahl Rikard, Lane David P., Leadbetter Elizabeth A., Karlsson Mikael C. I., Combined proinflammatory cytokine and cognate activation of invariant natural killer T cells enhances anti-DNA antibody responses, Proceedings of the National Academy of Sciences, 117, 16, 2020. Crossref

  14. Schweiger Helmut, Rejtő Judit, Hofbauer Christoph J., Berg Verena, Allacher Peter, Zwiauer Karl, Feistritzer Clemens, Schuster Gerhard, Ay Cihan, Reipert Birgit M., Pabinger Ingrid, Nonneutralizing FVIII-specific antibody signatures in patients with hemophilia A and in healthy donors, Blood Advances, 6, 3, 2022. Crossref

  15. Kibler Artur, Budeus Bettina, Küppers Ralf, Seifert Marc, The Splenic Marginal Zone in Children Is Characterized by a Subpopulation of CD27-Negative, Lowly IGHV-Mutated B Cells, Frontiers in Immunology, 13, 2022. Crossref

  16. Moon Sangphil, Janssens Ibo, Kim Kyung Hyun, Stijlemans Benoit, Magez Stefan, Radwanska Magdalena, Detrimental Effect of Trypanosoma brucei brucei Infection on Memory B Cells and Host Ability to Recall Protective B-cell Responses, The Journal of Infectious Diseases, 226, 3, 2022. Crossref

  17. Taylor Joshua A., Hutchinson Mark A., Gearhart Patricia J., Maul Robert W., Antibodies in action: the role of humoral immunity in the fight against atherosclerosis, Immunity & Ageing, 19, 1, 2022. Crossref

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