Understanding Antibody Responses in Early Life: Baby Steps towards Developing an Effective Influenza Vaccine

被引:4
|
作者
Clemens, Elene A. [1 ]
Alexander-Miller, Martha A. [1 ]
机构
[1] Wake Forest Sch Med, Dept Microbiol & Immunol, Winston Salem, NC 27101 USA
来源
VIRUSES-BASEL | 2021年 / 13卷 / 07期
基金
美国国家卫生研究院;
关键词
newborn; influenza virus; vaccine; B cell; Tfh; antibody; B-CELL RESPONSES; NEONATAL DENDRITIC CELLS; ORIGINAL ANTIGENIC SIN; IMMUNE-RESPONSES; MEMORY B; T-CELLS; NEUTRALIZING ANTIBODIES; BONE-MARROW; PLASMA-CELL; MATERNAL IMMUNIZATION;
D O I
10.3390/v13071392
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The immune system of young infants is both quantitatively and qualitatively distinct from that of adults, with diminished responsiveness leaving these individuals vulnerable to infection. Because of this, young infants suffer increased morbidity and mortality from respiratory pathogens such as influenza viruses. The impaired generation of robust and persistent antibody responses in these individuals makes overcoming this increased vulnerability through vaccination challenging. Because of this, an effective vaccine against influenza viruses in infants under 6 months is not available. Furthermore, vaccination against influenza viruses is challenging even in adults due to the high antigenic variability across viral strains, allowing immune evasion even after induction of robust immune responses. This has led to substantial interest in understanding how specific antibody responses are formed to variable and conserved components of influenza viruses, as immune responses tend to strongly favor recognition of variable epitopes. Elicitation of broadly protective antibody in young infants, therefore, requires that both the unique characteristics of young infant immunity as well as the antibody immunodominance present among epitopes be effectively addressed. Here, we review our current understanding of the antibody response in newborns and young infants and discuss recent developments in vaccination strategies that can modulate both magnitude and epitope specificity of IAV-specific antibody.
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收藏
页数:21
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