Transiently antigen-primed B cells return to naive-like state in absence of T-cell help.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 28429719.
- Also identified by DOI 10.1038/ncomms15072 and PMC identifier 5413946.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
The perspective that naive B-cell recognition of antigen in the absence of T-cell help causes cell death or anergy is supported by in vivo studies of B cells that are continuously exposed to self-antigens. However, intravital imaging suggests that early B-cell recognition of large foreign antigens may be transient. Whether B cells are tolerized or can be recruited into humoural immune responses following such encounters is not clear. Here we show that in the presence of T-cell help, single transient antigen acquisition is sufficient to recruit B cells into the germinal centre and induce memory and plasma cell responses. In the absence of T-cell help, transiently antigen-primed B cells do not undergo apoptosis in vivo; they return to quiescence and are recruited efficiently into humoural responses upon reacquisition of antigen and T-cell help.
Medical subject headings
- Antigens
- B-Lymphocytes
- Germinal Center
- Muramidase
- Ovalbumin
- T-Lymphocytes, Helper-Inducer