Antigen-specific immune responses to influenza vaccine in utero

被引:74
作者
Rastogi, Deepa
Wang, Chaodong
Mao, Xia
Lendor, Cynthia
Rothman, Paul B.
Miller, Rachel L.
机构
[1] Columbia Univ Coll Phys & Surg, Dept Med, Div Pulm Allergy & Crit Care Med, New York, NY 10032 USA
[2] Albert Einstein Coll Med, Childrens Hosp, New York, NY USA
[3] Jiangxi Prov Peoples Hosp, Dept Neurol, Nanchang, Peoples R China
[4] Univ Iowa, Dept Internal Med, Iowa City, IA USA
关键词
D O I
10.1172/JCI29466
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Initial immune responses to allergens may occur before birth, thereby modulating the subsequent development of atopy. This paradigm remains controversial, however, due to the inability to identify antigen-specific T cells in cord blood. The advent of MHC tetramers has revolutionized the detection of antigen-specific T cells. Tetramer staining of cord blood after CMV infection has demonstrated that effective CD8(+) antigen-specific immune responses can follow intrauterine viral infections. We hypothesized that sensitization to antigens occurs in utero in humans. We studied cord blood B and T cell immune responses following vaccination against influenza during pregnancy. Anti-Fluzone and anti-matrix protein IgM antibodies were detected in 38.5% (27 of 70) and 40.0% (28 of 70), respectively, of cord blood specimens. Using MHC tetramers, HA-specific CD4(+)T cells were detected among 25.0% (3 of 12) and 42.9% (6 of 14) of cord blood specimens possessing DRB1*0101 and DRB1*0401 HLA types, respectively, and were detected even when the DRB1 HLA type was inherited from the father. Matrix protein-specific CD8(+) T cells were detected among 10.0% (2 of 20) of HLA-A*0201(+) newborns. These results suggest that B and T cell immune responses occur in the fetus following vaccination against influenza and have important implications for determining when immune responses to environmental exposures begin.
引用
收藏
页码:1637 / 1646
页数:10
相关论文
共 56 条
[51]   Concurrent naive and memory CD8+ T cell responses to an influenza A virus [J].
Turner, SJ ;
Cross, R ;
Xie, WD ;
Doherty, PC .
JOURNAL OF IMMUNOLOGY, 2001, 167 (05) :2753-2758
[52]  
VANDERBEEKEN Y, 1985, AM J REPROD IM MIC, V8, P39
[53]   Frequencies of epitope-specific cytotoxic T lymphocytes in active chronic viral hepatitis B infection by using MHC class I peptide tetramers [J].
Wu, YZ ;
Zhang, JB ;
Chen, SY ;
Chen, A ;
Wang, L ;
Li, JY ;
Zhao, TT ;
Zou, LY ;
Tang, Y ;
Tingrong, L ;
Wang, F .
IMMUNOLOGY LETTERS, 2004, 92 (03) :253-258
[54]  
Yabuhara A, 1997, CLIN EXP ALLERGY, V27, P1261, DOI 10.1111/j.1365-2222.1997.tb01170.x
[55]   IN-VITRO PROLIFERATIVE RESPONSES OF HUMAN PERIPHERAL-BLOOD MONONUCLEAR-CELLS TO NON-RECALL ANTIGENS [J].
YOUNG, JL ;
DASER, A ;
BEVERLEY, PCL .
JOURNAL OF IMMUNOLOGICAL METHODS, 1995, 182 (02) :177-184
[56]   IDENTIFICATION OF THE HLA-DRB1-ASTERISK-04, HLA-DRB1-ASTERISK-07, AND HLA-DRB1-ASTERISK-09 ALLELES BY PCR AMPLIFICATION WITH SEQUENCE-SPECIFIC PRIMERS (PCR-SSP) IN 2 HOURS [J].
ZETTERQUIST, H ;
OLERUP, O .
HUMAN IMMUNOLOGY, 1992, 34 (01) :64-74