scholarly journals Deficiency of STING Promotes Collagen-Specific Antibody Production and B Cell Survival in Collagen-Induced Arthritis

2020 ◽  
Vol 11 ◽  
Author(s):  
Mookmanee Tansakul ◽  
Arthid Thim-uam ◽  
Thammakorn Saethang ◽  
Jiradej Makjaroen ◽  
Benjawan Wongprom ◽  
...  
1997 ◽  
Vol 185 (3) ◽  
pp. 551-562 ◽  
Author(s):  
Sanjiv A. Luther ◽  
Adam Gulbranson-Judge ◽  
Hans Acha-Orbea ◽  
Ian C.M. MacLennan

Mouse mammary tumor virus (MMTV[SW]) encodes a superantigen expressed by infected B cells. It evokes an antibody response specific for viral envelope protein, indicating selective activation of antigen-specific B cells. The response to MMTV(SW) in draining lymph nodes was compared with the response to haptenated chicken gamma globulin (NP-CGG) using flow cytometry and immunohistology. T cell priming occurs in both responses, with T cells proliferating in association with interdigitating dendritic cells in the T zone. T cell proliferation continues in the presence of B cells in the outer T zone, and B blasts then undergo exponential growth and differentiation into plasma cells in the medullary cords. Germinal centers develop in both responses, but those induced by MMTV(SW) appear later and are smaller. Most T cells activated in the T zone and germinal centers in the MMTV(SW) response are superantigen specific and these persist for weeks in lymph nodes draining the site MMTV(SW) injection; this contrasts with the selective loss of superantigen-specific T cells from other secondary lymphoid tissues. The results indicate that this viral superantigen, when expressed by professional antigen-presenting cells, drives extrafollicular and follicular B cell differentiation leading to virus-specific antibody production.


AIDS ◽  
1995 ◽  
Vol 9 (7) ◽  
pp. 695-700 ◽  
Author(s):  
Kristina Eriksson ◽  
Anders Kilander ◽  
Lars Hagberg ◽  
Gunnar Norkrans ◽  
Jan Holmgren ◽  
...  

2008 ◽  
Vol 181 (12) ◽  
pp. 8409-8415 ◽  
Author(s):  
Robert L. Schelonka ◽  
Michael Zemlin ◽  
Ryoki Kobayashi ◽  
Gregory C. Ippolito ◽  
Yingxin Zhuang ◽  
...  

Immunology ◽  
2014 ◽  
Vol 142 (4) ◽  
pp. 624-635 ◽  
Author(s):  
Eunju O ◽  
Eun-Ju Ko ◽  
Min-Chul Kim ◽  
Young-Tae Lee ◽  
Jae-Min Song ◽  
...  

1981 ◽  
Vol 154 (4) ◽  
pp. 1043-1057 ◽  
Author(s):  
H C Lane ◽  
D J Volkman ◽  
G Whalen ◽  
A S Fauci

A highly specific and reproducible antigen-induced, antigen-specific culture and assay system for antibody production by human peripheral blood B lymphocytes has been developed. The system is clearly T cell and monocyte dependent and is independent of exogenous mitogens. The major factors in our ability to trigger specific antibody production with antigen alone have been the use of extremely low concentrations of antigen in vitro (doses several orders of magnitude below those inducing a peak blastogenic response), careful attention to in vitro cell density and culture vessel geometry, and appreciation of the kinetics of the circulating antigen-inducible B cell repertoire. A dichotomy and overlap between antigen-induced, antigen-specific and antigen-induced, polyclonal responses was observed in the study of doubly immunized individuals. Whereas antibody responses highly specific for the antigen in culture were observed under one set of culture conditions (flat-bottomed vessels, 1.5 x 10(6) cells), switching to another culture system (round-bottomed vessels, 5 x 10(5) cells) resulted in polyclonal responses to antigen. Despite these culture condition-related differences in the induction of antibody synthesis, the suppression of specific antibody production that occurred at high concentrations of antigen was specific only for the antigen in culture. The capability to easily and reproducibly look at truly antigen-induced, antigen specific antibody production should be a major tool in furthering the understanding of human B cell activation and immunoregulation.


2016 ◽  
Vol 54 (12) ◽  
pp. 1343-1404
Author(s):  
V Khairnar ◽  
V Duhan ◽  
JR Göthert ◽  
PA Lang ◽  
BB Singer ◽  
...  

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