Postnatal innate immune Development: From Birth to Adulthood

被引:123
作者
Georgountzou, Anastasia [1 ]
Papadopoulos, Nikolaos G. [1 ,2 ]
机构
[1] Natl & Kapodistrian Univ Athens, Allergy & Clin Immunol Unit, Pediat Clin 2, Athens, Greece
[2] Univ Manchester, Div Infect Inflammat & Resp Med, Manchester, Lancs, England
关键词
innate immunity; postnatal development; innate ontogeny; immune trajectories; immune-related diseases; AGE-RELATED-CHANGES; TOLL-LIKE RECEPTORS; DENDRITIC CELL SUBSETS; HEALTHY-CHILDREN; EPITHELIAL-CELLS; CYTOKINE RESPONSES; HUMAN NEWBORN; SKIN BARRIER; INFANT SKIN; POLYMORPHONUCLEAR LEUKOCYTES;
D O I
10.3389/fimmu.2017.00957
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
It is well established that adaptive immune responses are deficient in early life, contributing to increased mortality and morbidity. The developmental trajectories of different components of innate immunity are only recently being explored. Individual molecules, cells, or pathways of innate recognition and signaling, within different compartments/anatomical sites, demonstrate variable maturation patterns. Despite some discrepancies among published data, valuable information is emerging, showing that the developmental pattern of cytokine responses during early life is age and toll-like receptor specific, and may be modified by genetic and environmental factors. Interestingly, specific environmental exposures have been linked both to innate function modifications and the occurrence of chronic inflammatory disorders, such as respiratory allergies. As these conditions are on the rise, our knowledge on innate immune development and its modulating factors needs to be expanded. Improved understanding of the sequence of events associated with disease onset and persistence will lead toward meaningful interventions. This review describes the state-of-the-art on normal postnatal innate immune ontogeny and highlights research areas that are currently explored or should be further addressed.
引用
收藏
页数:16
相关论文
共 228 条
[1]   Complex Biological Profile of Hematologic Markers across Pediatric, Adult, and Geriatric Ages: Establishment of Robust Pediatric and Adult Reference Intervals on the Basis of the Canadian Health Measures Survey [J].
Adeli, Khosrow ;
Raizman, Joshua E. ;
Chen, Yunqi ;
Higgins, Victoria ;
Nieuwesteeg, Michelle ;
Abdelhaleem, Mohamed ;
Wong, Suzy L. ;
Blais, David .
CLINICAL CHEMISTRY, 2015, 61 (08) :1075-1086
[2]   Neonatal adaptive immunity comes of age [J].
Adkins, B ;
Leclerc, C ;
Marshall-Clarke, S .
NATURE REVIEWS IMMUNOLOGY, 2004, 4 (07) :553-564
[3]   Age-dependent variation in the serum concentration of mannan-binding protein [J].
Aittoniemi, J ;
Miettinen, A ;
Laippala, P ;
Isolauri, E ;
Viikari, J ;
Ruuska, T ;
Soppi, E .
ACTA PAEDIATRICA, 1996, 85 (08) :906-909
[4]   Population-based pediatric reference intervals for hematology, iron and transferrin [J].
Aldrimer, Mattias ;
Ridefelt, Peter ;
Rodoo, Peo ;
Niklasson, Frank ;
Gustafsson, Jan ;
Hellberg, Dan .
SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION, 2013, 73 (03) :253-261
[5]   ASSESSMENT OF NEUTROPHIL CHEMOTAXIS AND RANDOM MIGRATION IN CHILDHOOD - COMPARISON BETWEEN LEADING-FRONT AND LOWER SURFACE COUNT METHODS [J].
ALNAKEEB, S ;
THOMPSON, EN .
ARCHIVES OF DISEASE IN CHILDHOOD, 1980, 55 (04) :296-298
[6]   Impaired Toll-like receptor 2 signalling in monocytes from 5-year-old allergic children [J].
Amoudruz, P. ;
Holmlund, U. ;
Saghafian-Hedengren, S. ;
Nilsson, C. ;
Sverremark-Ekstrom, E. .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2009, 155 (03) :387-394
[7]   ABNORMAL MOBILITY OF NEONATAL POLYMORPHONUCLEAR LEUKOCYTES - RELATIONSHIP TO IMPAIRED REDISTRIBUTION OF SURFACE-ADHESION SITES BY CHEMOTACTIC FACTOR OR COLCHICINE [J].
ANDERSON, DC ;
HUGHES, BJ ;
SMITH, CW .
JOURNAL OF CLINICAL INVESTIGATION, 1981, 68 (04) :863-874
[8]   Regulation of mucin expression: Mechanistic aspects and implications for cancer and inflammatory diseases [J].
Andrianifahanana, Mahefatiana ;
Moniaux, Nicolas ;
Batra, Surinder K. .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 2006, 1765 (02) :189-222
[9]  
BALLOW M, 1974, CLIN EXP IMMUNOL, V18, P257
[10]   The peptide antibiotic LL-37/hCAP-18 is expressed in epithelia of the human lung where it has broad antimicrobial activity at the airway surface [J].
Bals, R ;
Wang, XR ;
Zasloff, M ;
Wilson, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (16) :9541-9546