4.7 Article Book Chapter

Human B-1 cells take the stage

Journal

YEAR IN IMMUNOLOGY
Volume 1285, Issue -, Pages 97-114

Publisher

BLACKWELL SCIENCE PUBL
DOI: 10.1111/nyas.12137

Keywords

B-1; B cells; lymphocytes; antibody

Categories

Funding

  1. NIAID NIH HHS [R01 AI029690, R21 AI095787, R21 AI099517] Funding Source: Medline
  2. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R21AI095787, R01AI029690, R21AI099517] Funding Source: NIH RePORTER

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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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