4.6 Article

PDCA Expression by B Lymphocytes Reveals Important Functional Attributes

Journal

JOURNAL OF IMMUNOLOGY
Volume 184, Issue 2, Pages 807-815

Publisher

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.0902528

Keywords

-

Categories

Funding

  1. National Institutes of Health [RO1-EY013325]
  2. Arthritis Foundation
  3. National Cancer Center, Korea [NCC-0890830-2, NCC-0810720-2]
  4. Korean Science and Engineering Foundation [M10641000040, M 10870060009]
  5. Korean Research Foundation [KRF-2005-084-E00001]
  6. Korea Health 21 RD [A050260]

Ask authors/readers for more resources

We have demonstrated in this study the existence of a PDCA-expressing functional B cell population (PDCA(+) B lymphocytes), which differentiates from activated conventional B (PDCA(-)IgM(+)) lymphocytes. Stimulation with anti-mu, LIPS, CpG oligodeoxynucleotide, HSV-1, or CTLA-4 Ig activates the PDCA(+) B lymphocytes, leading to cell division and induction of type I IFNs and IDO. Notably, the PDCA(+) B lymphocytes are capable of Ag-specific Ab production and Ig class switching, which is corroborated by transfer experiments in B- and PDCA(+) B lymphocyte-deficient mu MT mice. Importantly, in lupus-prone MRL-Fas(lpr) mice, PDCA(+) B lymphocytes remain the principal source of autoantibodies. The PDCA(+) B lymphocytes have phenotypes with plasmacytoid dendritic cells, but are a distinct cell population in that they develop from C-kit(+)B220(+) pro-B precursors. Thus, our data suggest that not all PDCA(+) cells are dendritic cell-derived plasmacytoid dendritic cells and that a significant majority is the PDCA(+) B lymphocyte population having distinct phenotype and function. The Journal of Immunology, 2010, 184: 807-815.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available