Development of immunity in early life

被引:85
作者
Goenka, Anu [1 ]
Kollmann, Tobias R. [2 ]
机构
[1] Univ Manchester, Manchester Collaborat Ctr Inflammat Res, Core Technol Facil, Manchester M13 9NT, Lancs, England
[2] Univ British Columbia, Child & Family Res Inst, Vancouver, BC V5Z 4H4, Canada
关键词
Immunity; Ontogeny; Newborn; Infant; Development; TOLL-LIKE RECEPTORS; TNF-ALPHA PRODUCTION; LYMPHOCYTE SUBPOPULATIONS; COMPLEMENT-SYSTEM; REFERENCE VALUES; PRETERM INFANTS; NEONATAL-PERIOD; INNATE IMMUNITY; T-CELLS; RESPONSES;
D O I
10.1016/j.jinf.2015.04.027
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The immune system in early life goes through rapid and radical changes. Early life is also the period with the highest risk of infections. The foetal immune system is programmed to coexist with foreign antigenic influences in utero, and postnatally to rapidly develop a functional system capable of distinguishing helpful microbes from harmful pathogens. Both host genetics and environmental influences shape this dramatic transition and direct the trajectory of the developing immune system into early childhood and beyond. Given the malleability of the immune system in early life, interventions aimed at modulating this trajectory thus have the potential to translate into considerable reductions in infectious disease burden with immediate as well as long-lasting benefit. However, an improved understanding of the underlying molecular drivers of early life immunity is prerequisite to optimise such interventions and transform the window of early life vulnerability into one of opportunity. (C) 2015 The British Infection Association. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:S112 / S120
页数:9
相关论文
共 81 条
[51]   Nutritionally Mediated Programming of the Developing Immune System [J].
Palmer, Amanda C. .
ADVANCES IN NUTRITION, 2011, 2 (05) :377-395
[52]   Non-specific effects of vaccines: RCTs, not observational studies, are needed [J].
Pollard, Andrew J. .
ARCHIVES OF DISEASE IN CHILDHOOD, 2012, 97 (08) :677-678
[53]  
Poolman J, 2011, EXPERT REV VACCINES, V10, P307, DOI [10.1586/ERV.11.8, 10.1586/erv.11.8]
[54]   Association of Human TLR1 and TLR6 Deficiency with Altered Immune Responses to BCG Vaccination in South African Infants [J].
Randhawa, April Kaur ;
Shey, Muki S. ;
Keyser, Alana ;
Peixoto, Blas ;
Wells, Richard D. ;
de Kock, Marwou ;
Lerumo, Lesedi ;
Hughes, Jane ;
Hussey, Gregory ;
Hawkridge, Anthony ;
Kaplan, Gilla ;
Hanekom, Willem A. ;
Hawn, Thomas R. .
PLOS PATHOGENS, 2011, 7 (08)
[55]   Toll-like receptors and microbial exposure: gene-gene and gene-environment interaction in the development of atopy [J].
Reijmerink, N. E. ;
Kerkhof, M. ;
Bottema, R. W. B. ;
Gerritsen, J. ;
Stelma, F. F. ;
Thijs, C. ;
van Schayck, C. P. ;
Smit, H. A. ;
Brunekreef, B. ;
Postma, D. S. ;
Koppelman, G. H. .
EUROPEAN RESPIRATORY JOURNAL, 2011, 38 (04) :833-840
[56]   Ontogeny of Toll-Like Receptor Mediated Cytokine Responses of South African Infants throughout the First Year of Life [J].
Reikie, Brian A. ;
Adams, Rozanne C. M. ;
Ruck, Candice E. ;
Ho, Kevin ;
Leligdowicz, Aleksandra ;
Pillay, Santoshan ;
Naidoo, Shalena ;
Fortuno, Edgardo S., III ;
de Beer, Corena ;
Preiser, Wolfgang ;
Cotton, Mark F. ;
Speert, David P. ;
Esser, Monika ;
Kollmann, Tobias R. .
PLOS ONE, 2012, 7 (09)
[57]  
Ridings J, 1998, CLIN EXP IMMUNOL, V114, P33
[58]   Social mixing with other children during infancy enhances antibody response to a pneumococcal conjugate vaccine in early childhood [J].
Salt, Penny ;
Banner, Carly ;
Oh, Sarah ;
Yu, Ly-mee ;
Lewis, Susan ;
Pan, Dingxin ;
Griffiths, David ;
Ferry, Berne ;
Pollard, Andrew .
CLINICAL AND VACCINE IMMUNOLOGY, 2007, 14 (05) :593-599
[59]  
Schaub Bianca, 2009, J Allergy Clin Immunol, V123, P774, DOI 10.1016/j.jaci.2009.01.056
[60]   The inverse association between tuberculin responses and atopic disorder [J].
Shirakawa, T ;
Enomoto, T ;
Shimazu, S ;
Hopkin, JM .
SCIENCE, 1997, 275 (5296) :77-79