Sökning: WFRF:(Marcellini M) > The Interplay betwe...
Fältnamn | Indikatorer | Metadata |
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000 | 03998naa a2200793 4500 | |
001 | oai:gup.ub.gu.se/291199 | |
003 | SwePub | |
008 | 240528s2020 | |||||||||||000 ||eng| | |
024 | 7 | a https://gup.ub.gu.se/publication/2911992 URI |
024 | 7 | a https://doi.org/10.1016/j.celrep.2020.02.0222 DOI |
040 | a (SwePub)gu | |
041 | a eng | |
042 | 9 SwePub | |
072 | 7 | a ref2 swepub-contenttype |
072 | 7 | a art2 swepub-publicationtype |
100 | 1 | a Grimsholm, O.4 aut |
245 | 1 0 | a The Interplay between CD27(dull) and CD27(brig)(ht) B Cells Ensures the Flexibility, Stability, and Resilience of Human B Cell Memory |
264 | 1 | b Elsevier BV,c 2020 |
520 | a Memory B cells (MBCs) epitomize the adaptation of the immune system to the environment. We identify two MBC subsets in peripheral blood, CD27(dull) and CD27(bright) MBCs, whose frequency changes with age. Heavy chain variable region (VH) usage, somatic mutation frequency replacement-to-silent ratio, and CDR3 property changes, reflecting consecutive selection of highly antigen-specific, low cross-reactive antibody variants, all demonstrate that CD27(du)(ll) and CD27(bright) MBCs represent sequential MBC developmental stages, and stringent antigen-driven pressure selects CD27(du)(ll) into the CD27(bright) MBC pool. Dynamics of human MBCs are exploited in pregnancy, when 50% of maternal MBCs are lost and CD27(du)(ll) MBCs transit to the more differentiated CD27 bright stage. In the postpartum period, the maternal MBC pool is replenished by the expansion of persistent CD27(du)(ll) clones. Thus, the stability and flexibility of human B cell memory is ensured by CD27(du)(ll) MBCs that expand and differentiate in response to change. | |
650 | 7 | a MEDICIN OCH HÄLSOVETENSKAPx Medicinska och farmaceutiska grundvetenskaperx Cell- och molekylärbiologi0 (SwePub)301082 hsv//swe |
650 | 7 | a MEDICAL AND HEALTH SCIENCESx Basic Medicinex Cell and Molecular Biology0 (SwePub)301082 hsv//eng |
653 | a hyper-igm syndrome | |
653 | a neutralizing antibodies | |
653 | a somatic hypermutation | |
653 | a infections | |
653 | a activation | |
653 | a subsets | |
653 | a differentiation | |
653 | a proliferation | |
653 | a compartment | |
653 | a deficiency | |
653 | a Cell Biology | |
700 | 1 | a Mortari, E. P.4 aut |
700 | 1 | a Davydov, A. N.4 aut |
700 | 1 | a Shugay, M.4 aut |
700 | 1 | a Obraztsova, A. S.4 aut |
700 | 1 | a Bocci, C.4 aut |
700 | 1 | a Marasco, E.4 aut |
700 | 1 | a Marcellini, V.4 aut |
700 | 1 | a Aranburu, Alaitzu Gothenburg University,Göteborgs universitet,Institutionen för medicin, avdelningen för reumatologi och inflammationsforskning,Institute of Medicine, Department of Rheumatology and Inflammation Research4 aut0 (Swepub:gu)xaraal |
700 | 1 | a Farroni, C.4 aut |
700 | 1 | a Silvestris, D. A.4 aut |
700 | 1 | a Cristofoletti, C.4 aut |
700 | 1 | a Giorda, E.4 aut |
700 | 1 | a Scarsella, M.4 aut |
700 | 1 | a Cascioli, S.4 aut |
700 | 1 | a Barresi, S.4 aut |
700 | 1 | a Lougaris, V.4 aut |
700 | 1 | a Plebani, A.4 aut |
700 | 1 | a Cancrini, C.4 aut |
700 | 1 | a Finocchi, A.4 aut |
700 | 1 | a Moschese, V.4 aut |
700 | 1 | a Valentini, D.4 aut |
700 | 1 | a Vallone, C.4 aut |
700 | 1 | a Signore, F.4 aut |
700 | 1 | a de Vincentiis, G.4 aut |
700 | 1 | a Zaffina, S.4 aut |
700 | 1 | a Russo, G.4 aut |
700 | 1 | a Gallo, A.4 aut |
700 | 1 | a Locatelli, F.4 aut |
700 | 1 | a Tozzi, A. E.4 aut |
700 | 1 | a Tartaglia, M.4 aut |
700 | 1 | a Chudakov, D. M.4 aut |
700 | 1 | a Carsetti, R.4 aut |
710 | 2 | a Göteborgs universitetb Institutionen för medicin, avdelningen för reumatologi och inflammationsforskning4 org |
773 | 0 | t Cell Reportsd : Elsevier BVg 30:9q 30:9x 2211-1247 |
856 | 4 | u http://www.cell.com/article/S2211124720301765/pdf |
856 | 4 8 | u https://gup.ub.gu.se/publication/291199 |
856 | 4 8 | u https://doi.org/10.1016/j.celrep.2020.02.022 |
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