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Publication : Virus-induced maturation and activation of autoreactive memory B cells.

First Author  Reed AJ Year  2000
Journal  J Exp Med Volume  192
Issue  12 Pages  1763-74
PubMed ID  11120773 Mgi Jnum  J:250248
Mgi Id  MGI:6102638 Doi  10.1084/jem.192.12.1763
Citation  Reed AJ, et al. (2000) Virus-induced maturation and activation of autoreactive memory B cells. J Exp Med 192(12):1763-74
abstractText  We have examined B cell populations that participate in distinct phases of the immune response to the influenza virus A/PR/8/34 hemagglutinin (HA) for their susceptibility to negative selection in mice that express the HA as a neo-self-antigen (HA104 mice). We demonstrated previously that specificity for the neo-self-HA causes a population of immunoglobulin G antibody-secreting cells, which dominate the primary response to virus immunization in BALB/c mice, to be negatively selected in HA104 mice. We find here that in contrast to these primary response B cells, HA-specific memory response B cells developed equivalently in HA104 and nontransgenic (BALB/c) mice. Indeed, there was no indication that HA-specific B cells were negatively selected during memory formation in influenza virus-immunized HA104 mice, even though the neo-self-HA can be recognized by memory B cells. Furthermore, HA-specific autoantibodies were induced in the absence of virus immunization by mating HA104 mice with mice transgenic for a CD4(+) HA-specific T cell receptor. These findings indicate that specificity for a self-antigen does not prevent the maturation of autoreactive B cells in the germinal center pathway. Rather, the availability of CD4(+) T cell help may play a crucial role in regulating autoantibody responses to the HA in HA104 mice.
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