Evidence map›Paper›PMID 35522723›Full record

ArticleScience immunology2022

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

Masayuki Kuraoka, Chen-Hao Yeh, Goran Bajic, Ryutaro Kotaki, Shengli Song, Ian Windsor, Stephen C Harrison, Garnett Kelsoe

Abstract read
In one paragraph

Article in Science immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

48 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Observational
  5. Article
  6. Article
  7. Article
  8. Clonal dynamics of germinal center refueling by secondary immunization.bioRxiv : the preprint server for biology · 2026
    Article
  9. Article
  10. Extrafollicular and other non-germinal center B cell responses.Journal of immunology (Baltimore, Md. : 1950) · 2026
    Review
  11. The multilayered identity of B cell memory.Cellular & molecular immunology · 2026
    Review
  12. Review
  13. Review
  14. Article
  15. Local control of T cell fate in lymph nodes safely and durably reverses myelin-driven autoimmunity.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Masayuki KuraokaDepartment of Immunology, Duke University, Durham, NC, USA.ORCID 0000-0001-8745-6614
Chen-Hao YehDepartment of Immunology, Duke University, Durham, NC, USA.ORCID 0000-0001-5801-2918
Goran BajicLaboratory of Molecular Medicine, Children's Hospital, Harvard Medical School, Boston, MA, USA.ORCID 0000-0003-0480-4324
Ryutaro KotakiDepartment of Immunology, Duke University, Durham, NC, USA.ORCID 0000-0001-7965-1671
Shengli SongDepartment of Immunology, Duke University, Durham, NC, USA.
Ian WindsorLaboratory of Molecular Medicine, Children's Hospital, Harvard Medical School, Boston, MA, USA.ORCID 0000-0002-6289-6928
Stephen C HarrisonLaboratory of Molecular Medicine, Children's Hospital, Harvard Medical School, Boston, MA, USA.ORCID 0000-0001-7215-9393
Garnett KelsoeDepartment of Immunology, Duke University, Durham, NC, USA.ORCID 0000-0002-8770-040X

Funding

Virus biology scientific research support componentUM1AI100645 · NIAID · DUKE UNIVERSITY · PI MCMICHAEL, ANDREW JAMES · 2012 to 2018
$204.7M
Virus and Antibody Gene Sequencing CoreP01AI131251 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI Kevin Wiehe · 2017 to 2026
$40.7M
Virology CoreP01AI089618 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI Jiwon Lee · 2011 to 2026
$40.0M
NIAID NIH HHS P01 AI089618NIAID NIH HHS P01 AI131251NIAID NIH HHS UM1 AI100645
6 · The paper itself

Abstract

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 of immunization plays any role in memory B cell participation 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 after 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 after 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.

Indexed as

Germinal CenterImmunizationAntigensB-LymphocytesImmunity, HumoralVaccinationAntigens

Identifiers

PMID35522723
PMCPMC9169233

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.