Skip to main content

Lund University Publications

LUND UNIVERSITY LIBRARIES

Developmental changes in the rules for B cell selection*

Vergani, Stefano LU and Yuan, Joan LU orcid (2021) In Immunological Reviews 300(1). p.194-202
Abstract

The autoimmune checkpoint during B cell maturation eliminates self-antigen reactive specificities from the mature B cell repertoire. However, an exception to this rule is illustrated by B-1 cells, an innate-like self-reactive B cell subset that is positively selected into the mature B cell pool in a self-antigen-driven fashion. The mechanisms by which B-1 cells escape central tolerance have puzzled the field for decades. A key clue comes from their restricted developmental window during fetal and neonatal life. Here we use B-1 cells as a prototypic early life derived B cell subset to explore developmental changes in the constraints of B cell selection. We discuss recent advancements in the understanding of the molecular program,... (More)

The autoimmune checkpoint during B cell maturation eliminates self-antigen reactive specificities from the mature B cell repertoire. However, an exception to this rule is illustrated by B-1 cells, an innate-like self-reactive B cell subset that is positively selected into the mature B cell pool in a self-antigen-driven fashion. The mechanisms by which B-1 cells escape central tolerance have puzzled the field for decades. A key clue comes from their restricted developmental window during fetal and neonatal life. Here we use B-1 cells as a prototypic early life derived B cell subset to explore developmental changes in the constraints of B cell selection. We discuss recent advancements in the understanding of the molecular program, centered around the RNA binding protein Lin28b, that licenses self-reactive B-1 cell output during ontogeny. Finally, we speculate on the possible link between the unique rules of early life B cell tolerance and the establishment of B cell – microbial mutualism to propose an integrated model for how developmental and environmental cues come together to create a protective layer of B cell memory involved in neonatal immune imprinting.

(Less)
Please use this url to cite or link to this publication:
author
and
organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
B cell tolerance, B-1 cells, early life B cell memory, Lin28b, neonatal immune imprinting, window of opportunity
in
Immunological Reviews
volume
300
issue
1
pages
194 - 202
publisher
Wiley-Blackwell
external identifiers
  • pmid:33501672
  • scopus:85099747891
ISSN
0105-2896
DOI
10.1111/imr.12949
language
English
LU publication?
yes
id
18343f90-db35-41f6-8ba7-7f2e1d611937
date added to LUP
2021-02-02 11:09:55
date last changed
2024-09-19 15:49:13
@article{18343f90-db35-41f6-8ba7-7f2e1d611937,
  abstract     = {{<p>The autoimmune checkpoint during B cell maturation eliminates self-antigen reactive specificities from the mature B cell repertoire. However, an exception to this rule is illustrated by B-1 cells, an innate-like self-reactive B cell subset that is positively selected into the mature B cell pool in a self-antigen-driven fashion. The mechanisms by which B-1 cells escape central tolerance have puzzled the field for decades. A key clue comes from their restricted developmental window during fetal and neonatal life. Here we use B-1 cells as a prototypic early life derived B cell subset to explore developmental changes in the constraints of B cell selection. We discuss recent advancements in the understanding of the molecular program, centered around the RNA binding protein Lin28b, that licenses self-reactive B-1 cell output during ontogeny. Finally, we speculate on the possible link between the unique rules of early life B cell tolerance and the establishment of B cell – microbial mutualism to propose an integrated model for how developmental and environmental cues come together to create a protective layer of B cell memory involved in neonatal immune imprinting.</p>}},
  author       = {{Vergani, Stefano and Yuan, Joan}},
  issn         = {{0105-2896}},
  keywords     = {{B cell tolerance; B-1 cells; early life B cell memory; Lin28b; neonatal immune imprinting; window of opportunity}},
  language     = {{eng}},
  month        = {{01}},
  number       = {{1}},
  pages        = {{194--202}},
  publisher    = {{Wiley-Blackwell}},
  series       = {{Immunological Reviews}},
  title        = {{Developmental changes in the rules for B cell selection*}},
  url          = {{http://dx.doi.org/10.1111/imr.12949}},
  doi          = {{10.1111/imr.12949}},
  volume       = {{300}},
  year         = {{2021}},
}