Age-associated B cells expanded in autoimmune mice are memory cells sharing H-CDR3-selected repertoires.

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Age-associated B cells expanded in autoimmune mice are memory cells sharing H-CDR3-selected repertoires.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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Age-associated B cells expande ...... g H-CDR3-selected repertoires.

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Age-associated B cells expande ...... g H-CDR3-selected repertoires.

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Age-associated B cells expande ...... g H-CDR3-selected repertoires.

@en

Age-associated B cells expande ...... g H-CDR3-selected repertoires.

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Age-associated B cells expande ...... g H-CDR3-selected repertoires.

@en

Age-associated B cells expande ...... g H-CDR3-selected repertoires.

@nl

P1476

Age-associated B cells expande ...... ng H-CDR3-selected repertoires

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P2093

Alaitz Aranburu

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Bjorn Corleis

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Hans Carlsten

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Nina Höök

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Weicheng Ren

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P2860

Expression of the immunoregulatory molecule FcRH4 defines a distinctive tissue-based population of memory B cells

Age-Associated B Cells: A T-bet-Dependent Effector with Roles in Protective and Pathogenic Immunity

A B-cell subset uniquely responsive to innate stimuli accumulates in aged mice

Toll-like receptor 7 (TLR7)-driven accumulation of a novel CD11c⁺ B-cell population is important for the development of autoimmunity

CD11c-Expressing B Cells Are Located at the T Cell/B Cell Border in Spleen and Are Potent APCs

A germinal center-independent pathway generates unswitched memory B cells early in the primary response

Both IgM and IgG anti-DNA antibodies are the products of clonally selective B cell stimulation in (NZB x NZW)F1 mice.

Presence of anti-Sm reactivity in autoimmune mouse strains.

FLICE-inhibitory protein is a key regulator of germinal center B cell apoptosis.

A Temporal Switch in the Germinal Center Determines Differential Output of Memory B and Plasma Cells.

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509-521

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scholarly article

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10.1002/EJI.201747127

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English

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Natalija Gerasimčik

Inga-Lill Martensson

Ola Grimsholm

Alessandro Camponeschi

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2018-01-15T00:00:00Z

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29266242

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