A subset of follicular helper-like MAIT cells can provide B cell help and support antibody production in the mucosa

2022 ◽  
Vol 7 (67) ◽  
Author(s):  
Owen Jensen ◽  
Shubhanshi Trivedi ◽  
Jeremy D. Meier ◽  
Keke C. Fairfax ◽  
J. Scott Hale ◽  
...  

We identify a MAIT cell subset expressing T follicular helper markers and show the ability of MAIT cells to support B cell responses in the mucosa.

Author(s):  
Francesca Schena ◽  
Federica Penco ◽  
Stefano Volpi ◽  
Claudia Pastorino ◽  
Roberta Caorsi ◽  
...  

Immunity ◽  
2014 ◽  
Vol 41 (6) ◽  
pp. 1026-1039 ◽  
Author(s):  
Peter T. Sage ◽  
Alison M. Paterson ◽  
Scott B. Lovitch ◽  
Arlene H. Sharpe

1982 ◽  
Vol 156 (2) ◽  
pp. 634-639 ◽  
Author(s):  
D J Volkman ◽  
A Ahmad ◽  
A S Fauci ◽  
D M Neville

The feasibility of selectively eliminating human antigen-specific B cell responses by treating cells in vitro with antigen covalently linked to a cell toxin was examined. Tetanus toxoid (TT) was conjugated to the toxin ricin via a thioether linkage. Peripheral blood mononuclear cells from recently immunized subjects were preincubated for 2 h with TT-ricin in the presence of lactose. Antigen was then removed, and the cells from recently immunized subjects were preincubated for 2 h with TT-ricin in the presence of lactose. Antigen was then removed, and the cells were stimulated with pokeweed mitogen to induce antibody production. TT-specific antibody production was completely abrogated by preincubation with TT-ricin but not by TT alone or a mixture of TT and ricin. In contrast, polyclonal immunoglobulin production was not diminished by TT-ricin. This selective abrogation was also seen when B cells alone were preincubated with TT-ricin and a source of T cell help was later provided. T cell blastogenic responses to TT remained intact after TT-ricin exposure. Thus, antigen-toxin conjugates are capable of selectively eliminating specific antibody-producing B cell clones, while leaving intact the remainder of the B cell repertoire.


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