Human B-1 cells take the stage.

Ann N Y Acad Sci

Center for Oncology and Cell Biology, The Feinstein Institute for Medical Research, Manhasset, NY, USA.

Published: May 2013

AI Article Synopsis

  • B-1 cells are essential for fighting off infections and clearing out dead cells, distinguishing themselves from conventional B-2 cells by their unique functions and the natural antibodies they secrete.
  • While originally studied in mice, researchers have now identified human B-1 cells using specific markers (CD20(+)CD27(+)CD43(+)CD70(-)) present in umbilical cord and adult blood.
  • Human B-1 cells have the potential to impact various diseases, particularly in older adults, and may offer new strategies for enhancing immune responses or treating immune-related conditions through the manipulation of their activity.

Article Abstract

B-1 cells play critical roles in defending against microbial invasion and in housekeeping removal of cellular debris. B-1 cells secrete natural antibody and manifest functions that influence T cell expansion and differentiation and in these and other ways differ from conventional B-2 cells. B-1 cells were originally studied in mice where they are easily distinguished from B-2 cells, but their identity in the human system remained poorly defined for many years. Recently, functional criteria for human B-1 cells were established on the basis of murine findings, and reverse engineering resulted in identification of the phenotypic profile, CD20(+)CD27(+)CD43(+)CD70(-), for B-1 cells found in both umbilical cord blood and adult peripheral blood. Human B-1 cells may contribute to multiple disease states through production of autoantibody and stimulation/modulation of T cell activity. Human B-1 cells could be a rich source of antibodies useful in treating diseases present in elderly populations where natural antibody protection may have eroded. Manipulation of human B-1 cell numbers and/or activity may be a new avenue for altering T cell function and treating immune dyscrasias.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4429725PMC
http://dx.doi.org/10.1111/nyas.12137DOI Listing

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