Recall of B cell memory depends on relative locations of prime and boost immunization.

Recall of B cell memory depends on relative locations of prime and boost immunization.
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DOI:
10.1126/sciimmunol.abn5311
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发表时间:
2022-05-06
期刊:
影响因子:
24.8
通讯作者:
Kelsoe, Garnett
Kelsoe, Garnett
中科院分区:
医学1区
文献类型:
--
作者:
Kuraoka, Masayuki;Yeh, Chen-Hao;Bajic, Goran;Kotaki, Ryutaro;Song, Shengli;Windsor, Ian;Harrison, Stephen C.;Kelsoe, Garnett

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Immunization or microbial infection can establish long-term B cell memory not only systemically but also locally. Evidence has suggested that local B cell memory contributes to early local plasmacytic responses after secondary challenge, however; it is unclear whether locality plays any role in participation of memory B cells in recall germinal centers (GCs) which is essential for updating their B cell antigen receptors (BCRs). Using single B cell culture and fate-mapping, we have characterized BCR repertoires in recall GCs following boost immunizations at sites local or distal to the priming. Local boosts with homologous antigen recruit the progeny of primary GC B cells to recall GCs more efficiently than do distal boosts. Recall GCs elicited by local boosts contain significantly more B cells with elevated levels of Immunoglobulin (Ig) mutation and higher avidity BCRs. This local preference is unaffected by blocking CD40:CD154 interaction to terminate active, GC responses. Local boosts with heterologous antigens elicit secondary GCs with B cell populations enriched for cross-reactivity to the prime and boost antigens; in contrast, cross-reactive GC B cells are rare following distal boosts. Our results suggest that local B cell memory is retained in the form of memory B cells, GC B cells and GC-phenotype B cells that are independent of organized GC structures and that these persistent “primed B cells” contribute to recall GC responses at local sites. Our findings indicate the importance of locality in humoral immunity and inform serial vaccination strategies for evolving viruses. The participation of memory B cells in recall germinal centers depends on whether the boost is local or distal to the priming site.
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