Differential effect of CD4+Foxp3+ T-regulatory cells on the B and T helper cell responses to influenza virus vaccination

被引:26
作者
Surls, Jacqueline [1 ]
Nazarov-Stoica, Cristina [1 ]
Kehl, Margaret [1 ]
Casares, Sofia [1 ,2 ]
Brumeanu, Teodor-D. [1 ]
机构
[1] Uniformed Serv Univ Hlth Sci, Dept Med, Div Immunol, Bethesda, MD 20814 USA
[2] USN, Med Res Ctr, Infect Dis Directorate, Silver Spring, MD 20910 USA
关键词
Influenza virus; Foxp3(+) T-regulatory cells; Vaccination; Immune responses; IMMUNOLOGICAL SELF-TOLERANCE; HUMAN-IMMUNODEFICIENCY-VIRUS; DENDRITIC CELLS; MEMORY CELLS; CLASS-I; CD4(+); INFECTION; RECEPTOR; ANTIGEN; SUPPRESSION;
D O I
10.1016/j.vaccine.2010.08.074
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The T-regulatory (T-reg) cells restrict the T-cell functions in various viral infections including influenza infection. However little is known about the effect of T-regs in influenza vaccination. Herein, we found that immunization of BALB/c mice with a prototype of UV-inactivated influenza PR8/A/34 virus vaccine expanded the CD4(+)Foxp3(+) T-reg pool and fostered the development of virus-specific CD4(+)Foxp3(+) T-reg cells. Increasing the size of Foxp3(+) T-reg pool did not alter the primary PR8-specific B-cell response, but it did suppress the primary and memory PR8-specific T helper responses induced by vaccination. In contrast, the vaccination-induced T helper cell response was augmented in the absence of CD4(+)Foxp3(+) T-reg cells. Since CD4 T helper cells contribute to anti-influenza protection, therapeutic "quenching" of T-reg function prior to vaccination may enhance the efficacy of influenza vaccination. Published by Elsevier Ltd.
引用
收藏
页码:7319 / 7330
页数:12
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