JCB logo
R&D Systems: New Poster Available
  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents

Published online 25 August 2003. doi:10.1083/jcb1625rr5
This Article
Right arrow PPT slides of all figures
Right arrow Alert me when this article is cited
Services
Right arrow Email this article
Right arrow Similar articles in this journal
Right arrow Alert me to new content in the JCB
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by LeBrasseur, N.
Right arrow Search for Related Content
PubMed
Right arrow Articles by LeBrasseur, N.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Facebook   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

© The Rockefeller University Press, 0021-9525/2003/9/751-b $5.00
The Journal of Cell Biology, Volume 162, Number 5, 751-b-751


Research Roundup

Losing self-awareness



Most self-reactive antibodies (green) are filtered from the developing immune system.

Nussenzweig/AAAS

Waste is rife in the immune system, based on a report from Hedda Wardemann, Michel Nussenzweig (Rockefeller University, New York, NY), and colleagues. The group has determined that more than half of the human B cell antibody population is removed before maturation.

The removal is a consequence of antibody gene rearrangement—a random process that is certain to generate some autoreactive antibodies. Nussenzweig's group now shows just how often autoreactivity occurs by identifying autoreactive B cells at different stages of development. Between 55% and 75% of the antibodies made by early immature B cells react against self antigens. These potentially dangerous antibodies are removed from the repertoire at two checkpoints: the number of self-reactive antibody-producing B cells were halved from within the bone marrow and then halved again after entering the blood stream. Also, nearly 90% of developing B cells producing polyreactive antibodies, whose promiscuity is probably a risk to the host, were removed at the marrow checkpoint.These studies will help determine how autoimmune diseases arise. "Any problem in the checkpoints that would allow self-reactive B cells to get through might be dangerous," says Wardemann. "We determined the numbers in normal, healthly donors. If we compare this to autoimmune patients, we should get an idea of where the problem lies." {blacksquare}

Reference:

Wardemann, H., et al. 2003. Science. 10.1126/science.1086907.



Nicole LeBrasseur

lebrasn{at}rockefeller.edu


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Facebook Facebook   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?



This Article
Right arrow PPT slides of all figures
Right arrow Alert me when this article is cited
Services
Right arrow Email this article
Right arrow Similar articles in this journal
Right arrow Alert me to new content in the JCB
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by LeBrasseur, N.
Right arrow Search for Related Content
PubMed
Right arrow Articles by LeBrasseur, N.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Facebook   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?


  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents