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T CELL RECEPTOR, HLA DISPARITY, & SUCCESSFUL PREGNANCY

T CELL RECEPTOR, HLA DISPARITY, & SUCCESSFUL PREGNANCY
T 细胞受体、HLA 差异、
批准号:
2457845
负责人:
J. Lee Nelson
金额:
$19.59万
依托单位国家:
美国
项目类别:
财政年份:
1995
资助国家:
美国
项目状态:
已结题
起止时间:
1995-08-01 至 1999-07-31

项目摘要

项目成果

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中文摘要
翻译
三分子复合物是免疫反应的基石
英文摘要
The trimolecular complex is a cornerstone of immunologic responsiveness and includes an HLA molecule, peptide antigen, and the T cell receptor. From the point of view of transplantation in which HLA incompatibility is associated with graft rejection, how the HLA disparate fetus escapes rejection is an intriguing unsolved question of immunology. Local factors at the maternal-fetal interface are likely to be key aspects of pregnancy success. Despite local factors, however, some fetal cells escape into the maternal circulation. The striking remission during pregnancy of rheumatoid arthritis indicates that effects on the maternal system can be systemic. Rheumatoid arthritis is an autoimmune disorder and is characterized by an association with particular HLA class II alleles. We have recently demonstrated that amelioration of this autoimmune disease is associated with fetal-maternal disparity for HLA class II antigens. The results of these studies (and others) have led us to postulate that the maternal T cell repertoire undergoes changes during pregnancy in response to fetal HLA peptides that enter the maternal circulation. During the 3 to 6 months postpartum rheumatoid arthritis returns virtually without exception. We propose to test the hypothesis that significant changes occur in the maternal T cell repertoire during pregnancy and after delivery. We expect that these changes will be particularly apparent around parturition. It is the purpose of the studies described in this proposal to characterize alpha-beta and gamma-delta T cell receptor usage around parturition, before, during and after pregnancy. From the fetal perspective pregnancies of RA women are excellent. Thus this autoimmune disease affords a human model in which a systemic effect is observed during pregnancy: a model from which insights may be gained bi- directionally about an enigmatic autoimmune disease that favors women and about successful pregnancy in which the fetal allograft thrives.
期刊论文(10)
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DOI: 10.1093/oxfordjournals.molbev.a026227
发表时间: 2000
期刊: Molecular biology and evolution
影响因子: 10.7
作者: [M. Richards;J. Nelson]
通讯作者: M. Richards;J. Nelson
Microchimerism: implications for autoimmune disease.
微嵌合现象:对自身免疫性疾病的影响。
DOI: 10.1177/096120339900800508
发表时间: 1999
期刊: Lupus
影响因子: 2.6
作者: [Nelson,JL]
通讯作者: Nelson,JL
Chimerism in transplantation and in spontaneously occurring autoimmune disease.
移植和自发发生的自身免疫性疾病中的嵌合现象。
DOI: 10.1016/s0041-1345(98)01775-8
发表时间: 1999
期刊: Transplantation proceedings
影响因子: 0.9
作者: [Nelson,JL]
通讯作者: Nelson,JL
Non-host cells in the pathogenesis of autoimmune disease: a new paradigm?
非宿主细胞在自身免疫性疾病发病机制中的作用:新范式?
DOI: 10.1136/ard.58.9.518
发表时间: 1999
期刊: Annals of the rheumatic diseases
影响因子: 27.4
作者: [Nelson,JL]
通讯作者: Nelson,JL
The Brain and Maternal Microchimerism
The Brain and Maternal Microchimerism
  • 批准号:
    10610125
  • 项目类别:
  • 资助金额:
    $23.18万
  • 财政年份:
    2021
  • 负责人:
    J. Lee Nelson
  • 依托单位:
Cancer in the Immunosuppressed Host
Cancer in the Immunosuppressed Host
  • 批准号:
    10602868
  • 项目类别:
  • 资助金额:
    $0.44万
  • 财政年份:
    2018
  • 负责人:
    J. Lee Nelson
  • 依托单位:
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