Document Detail


Pregnancy induces a fetal antigen-specific maternal T regulatory cell response that contributes to tolerance.
MedLine Citation:
PMID:  20439708     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
A fetus is inherently antigenic to its mother and yet is not rejected. The T regulatory (Treg) subset of CD4(+) T cells can limit immune responses and has been implicated in maternal tolerance of the fetus. Using virgin inbred mice undergoing a first syngenic pregnancy, in which only the male fetuses are antigenic, we demonstrate a maternal splenocyte proliferative response to the CD4(+) T cell restricted epitope of the male antigen (H-Y) in proportion to the fetal antigen load. A portion of the maternal immune response to fetal antigens is Treg in nature. The bystander suppressive function of pregnancy-generated Tregs requires the presence of the fetal antigen, demonstrating their inherent antigen specificity. In vivo targeting of diphtheria toxin to kill Tregs leads to a lower fraction of live male offspring and a selective reduction in mass of the surviving males. Thus, Tregs generated in the context of pregnancy function in an antigen-specific manner to limit the maternal immune response to the fetus in a successful pregnancy.
Authors:
Daniel A Kahn; David Baltimore
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't     Date:  2010-05-03
Journal Detail:
Title:  Proceedings of the National Academy of Sciences of the United States of America     Volume:  107     ISSN:  1091-6490     ISO Abbreviation:  Proc. Natl. Acad. Sci. U.S.A.     Publication Date:  2010 May 
Date Detail:
Created Date:  2010-05-20     Completed Date:  2010-07-22     Revised Date:  2010-11-22    
Medline Journal Info:
Nlm Unique ID:  7505876     Medline TA:  Proc Natl Acad Sci U S A     Country:  United States    
Other Details:
Languages:  eng     Pagination:  9299-304     Citation Subset:  IM    
Affiliation:
Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, David Geffen School of Medicine, University of California, Los Angeles, CA 90095-1740, USA.
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MeSH Terms
Descriptor/Qualifier:
Analysis of Variance
Animals
Cell Proliferation
DNA Primers / genetics
Epitopes / immunology
Female
H-Y Antigen / immunology*
Histocompatibility, Maternal-Fetal / immunology*
Immune Tolerance / immunology*
Male
Mice
Mice, Inbred C57BL
Polymerase Chain Reaction
Pregnancy
Spleen / cytology,  immunology
T-Lymphocytes, Regulatory / immunology*
Grant Support
ID/Acronym/Agency:
K12 HD001400/HD/NICHD NIH HHS
Chemical
Reg. No./Substance:
0/DNA Primers; 0/Epitopes; 0/H-Y Antigen

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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