Pattern recognition receptor-mediated cytokine response in infants across 4 continents

Journal of Allergy and Clinical Immunology

Volumn 133, Issue 3, 2014, Pages

  Smolen, Kinga K ^a   Ruck, Candice E ^a   Fortuno III, Edgardo S ^a   Ho, Kevin ^a   Dimitriu, Pedro ^a   Mohn, William W ^a   Speert, David P ^a   Cooper, Philip J ^b,c,d   Esser, Monika ^e   Goetghebuer, Tessa ^f   Marchant, Arnaud ^g   Kollmann, Tobias R ^a  

^a UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^b Centro de Investigaciones FEPIS   (Ecuador)

^c LIVERPOOL SCHOOL OF TROPICAL MEDICINE   (United Kingdom)

^d PONTIFICIA UNIVERSIDAD CATÓLICA DEL ECUADOR   (Ecuador)

^e STELLENBOSCH UNIVERSITY   (South Africa)

^f SAINT PIERRE UNIVERSITY HOSPITAL   (Belgium)

^g UNIVERSITÉ LIBRE DE BRUXELLES   (Belgium)

Author keywords

global; immune development; infectious disease; Innate immunity

Indexed keywords

CASPASE RECRUITMENT DOMAIN PROTEIN 15; CYTOKINE; PATTERN RECOGNITION RECEPTOR; TOLL LIKE RECEPTOR 2; TOLL LIKE RECEPTOR 4;

ADAPTIVE IMMUNITY; ARTICLE; BLOOD CULTURE; CHILD; CHILD HEALTH; CLINICAL OBSERVATION; CONTROLLED STUDY; CYTOKINE RESPONSE; ENVIRONMENTAL EXPOSURE; EUROPE; GENE EXPRESSION; HUMAN; INFANT; INFECTION SENSITIVITY; INNATE IMMUNITY; NORTH AMERICA; PRESCHOOL CHILD; PRIORITY JOURNAL; SOUTH AMERICA; VACCINATION;

GLOBAL; IMMUNE DEVELOPMENT; INFECTIOUS DISEASE; INNATE IMMUNITY;

CHILD, PRESCHOOL; CYTOKINES; DISEASE SUSCEPTIBILITY; HUMANS; IMMUNITY, INNATE; INFANT; INFANT MORTALITY; INFECTION; RECEPTORS, PATTERN RECOGNITION; TOLL-LIKE RECEPTORS;

EID: 84896709686     PISSN: 00916749     EISSN: 10976825     Source Type: Journal    
DOI: 10.1016/j.jaci.2013.09.038     Document Type: Article

References (43)

1. D.B. Lewis, and C.B. Wilson Developmental immunology and role of host defenses in fetal and neonatal susceptibility to infection J.S. Remington, C.B. Wilson, C.J. Baker, Infectious diseases of the fetus and newborn infant 7th ed. 2011 Elsevier Saunders Philiadelphia 80 191
2. M.K. Hostetter What we don't see N Engl J Med 366 2012 1328 1334
3. R.E. Black, S.S. Morris, and J. Bryce Where and why are 10 million children dying every year? Lancet 361 2003 2226 2234
4. O. Levy, S. Goriely, and T.R. Kollmann Immune response to vaccine adjuvants during the first year of life Vaccine 31 2013 2500 2505
5. T.R. Kollmann, O. Levy, R.R. Montgomery, and S. Goriely Innate immune function by Toll-like receptors: distinct responses in newborns and the elderly Immunity 37 2012 771 783
6. M.M. Levine "IDEAL" vaccines for resource poor settings Vaccine 29 2011 D116 D125
7. Core information for the development of immunization policy. Geneva: World Health Organization; 2003. Available from: https://extranet.who.int/aim- elearning/en/vaccines/hepb/pdf/www557.pdf. Accessed November 14, 2013.
8. M.M. Levine, and R. Robins-Browne Vaccines, global health and social equity Immunol Cell Biol 87 2009 274 278
9. L. Arevshatian, C. Clements, S. Lwanga, A. Misore, P. Ndumbe, and J. Seward et al. An evaluation of infant immunization in Africa: is a transformation in progress? Bull World Health Organ 85 2007 449 457
10. G.A. Poland, I.G. Ovsyannikova, and R.M. Jacobson Vaccine immunogenetics: bedside to bench to population Vaccine 26 2008 6183 6188
11. J. Clemens, and L. Jodar Introducing new vaccines into developing countries: obstacles, opportunities and complexities Nat Med 11 2005 S12 S15
12. T.R. Kollmann, J. Crabtree, A. Rein-Weston, D. Blimkie, F. Thommai, and X.Y. Wang et al. Neonatal innate TLR-mediated responses are distinct from those of adults J Immunol 183 2009 7150 7160
13. P.J. Cooper, M.E. Chico, I. Guadalupe, C.A. Sandoval, E. Mitre, and T.A. Platts-Mills et al. Impact of early life exposures to geohelminth infections on the development of vaccine immunity, allergic sensitization, and allergic inflammatory diseases in children living in tropical Ecuador: the ECUAVIDA birth cohort study BMC Infect Dis 11 2011 184
14. A.L. Slogrove, M.F. Cotton, and M.M. Esser Severe infections in HIV-exposed uninfected infants: clinical evidence of immunodeficiency J Trop Pediatr 56 2010 75 81
15. S.E. Turvey, and D.H. Broide Innate immunity J Allergy Clin Immunol 125 2010 S24 S32
16. J.E. Graham, L.M. Christian, and J.K. Kiecolt-Glaser Stress, age, and immune function: toward a lifespan approach J Behav Med 29 2006 389 400
17. D. Blimkie, E.S. Fortuno III, H. Yan, P. Cho, K. Ho, and S.E. Turvey et al. Variables to be controlled in the assessment of blood innate immune responses to Toll-like receptor stimulation J Immunol Methods 366 2011 89 99
18. K. Jansen, D. Blimkie, J. Furlong, A. Hajjar, A. Rein-Weston, and J. Crabtree et al. Polychromatic flow cytometric high-throughput assay to analyze the innate immune response to Toll-like receptor stimulation J Immunol Methods 336 2008 183 192
19. N.P. Corbett, D. Blimkie, K.C. Ho, B. Cai, D.P. Sutherland, and A. Kallos et al. Ontogeny of Toll-like receptor mediated cytokine responses of human blood mononuclear cells PLoS One 5 2010 e15041
20. B.A. Reikie, R.C. Adams, C.E. Ruck, K. Ho, A. Leligdowicz, and S. Pillay et al. Ontogeny of Toll-like receptor mediated cytokine responses of South African infants throughout the first year of life PLoS One 7 2012 e44763
21. M. De Caceres, F. Oliva, X. Font, and S. Vives Ginkgo, a program for non-standard multivariate fuzzy analysis Adv Fuzzy Sets Systems 2 2007 41 56
22. G. Bouxin Ginkgo, a multivariate analysis package J Veg Sci 16 2005 353 359
23. WHO Anthro. 2011. Available from: http://www.who.int/childgrowth/ software/en/. Accessed January 2011.
24. K.L. Flanagan, S. Burl, B.L. Lohman-Payne, and M. Plebanski The challenge of assessing infant vaccine responses in resource-poor settings Expert Rev Vaccines 9 2010 665 674
25. World Health Organization WHO child growth standards: head circumference for-age, arm circumference-for age, triceps skinfold-for-age and subscapular skinfold-for-age - methods and development 2007 World Health Organization Geneva
26. D.C. Shih, K.C. Ho, K.M. Melnick, R.A. Rensink, T.R. Kollmann, and E.S. Fortuno III Facilitating the analysis of immunological data with visual analytic techniques J Vis Exp 47 2011 pii:2397
27. B. Pulendran, and R. Ahmed Immunological mechanisms of vaccination Nat Immunol 12 2011 509 517
28. T.R. Kollmann Variation between populations in the innate immune response to vaccine adjuvants Front Immunol 4 2013 81
29. M. Nguyen, E. Leuridan, T. Zhang, D. De Wit, F. Willems, and P. Van Damme et al. Acquisition of adult-like TLR4 and TLR9 responses during the first year of life PLoS One 5 2010 e10407
30. M.E. Belderbos, G.M. van Bleek, O. Levy, M.O. Blanken, M.L. Houben, and L. Schuijff et al. Skewed pattern of Toll-like receptor 4-mediated cytokine production in human neonatal blood: low LPS-induced IL-12p70 and high IL-10 persist throughout the first month of life Clin Immunol 133 2009 228 237
31. R. Teran, E. Mitre, M. Vaca, S. Erazo, G. Oviedo, and M.P. Hubner et al. Immune system development during early childhood in tropical Latin America: evidence for the age-dependent down regulation of the innate immune response Clin Immunol 138 2011 299 310
32. A.H. van den Biggelaar, S.L. Prescott, M. Roponen, M.A. Nadal-Sims, C.J. Devitt, and S. Phuanukoonnon et al. Neonatal innate cytokine responses to BCG controlling T-cell development vary between populations J Allergy Clin Immunol 124 2009 544 550 550, e1-2
33. J.G. Lisciandro, S.L. Prescott, M.G. Nadal-Sims, C.J. Devitt, W. Pomat, and P.M. Siba et al. Ontogeny of Toll-like and NOD-like receptor-mediated innate immune responses in Papua New Guinean infants PLoS One 7 2012 e36793
34. J.G. Lisciandro, S.L. Prescott, M.G. Nadal-Sims, C.J. Devitt, P.C. Richmond, and W. Pomat et al. Neonatal antigen-presenting cells are functionally more quiescent in children born under traditional compared with modern environmental conditions J Allergy Clin Immunol 130 2012 1167 1174.e10
35. P.E. Fine Variation in protection by BCG: implications of and for heterologous immunity Lancet 346 1995 1339 1345
36. Y. Djuardi, E. Sartono, H. Wibowo, T. Supali, and M. Yazdanbakhsh A longitudinal study of BCG vaccination in early childhood: the development of innate and adaptive immune responses PLoS One 5 2010 e14066
37. Y. Djuardi, L.J. Wammes, T. Supali, E. Sartono, and M. Yazdanbakhsh Immunological footprint: the development of a child's immune system in environments rich in microorganisms and parasites Parasitology 138 2011 1508 1518
38. M.G. Netea, and J.W. van der Meer Immunodeficiency and genetic defects of pattern-recognition receptors N Engl J Med 364 2011 60 70
39. P. Cho, L. Gelinas, N.P. Corbett, S.J. Tebbutt, S.E. Turvey, and E.S. Fortuno III et al. Association of common single-nucleotide polymorphisms in innate immune genes with differences in TLR-induced cytokine production in neonates Genes Immun 14 2013 199 211
40. M.C. Collado, M. Cernada, C. Bauerl, M. Vento, and G. Perez-Martinez Microbial ecology and host-microbiota interactions during early life stages Gut Microbes 3 2012 352 365
41. E.M. Brown, M. Sadarangani, and B.B. Finlay The role of the immune system in governing host-microbe interactions in the intestine Nat Immunol 14 2013 660 667
42. United Nations, Department of Economic and Social Affairs, Population Division (2011). World population prospects: The 2010 revision, DVD edition.
43. H. Blencowe, S. Cousens, M.Z. Oestergaard, D. Chou, A.B. Moller, and R. Narwal et al. National, regional, and worldwide estimates of preterm birth rates in the year 2010 with time trends since 1990 for selected countries: a systematic analysis and implications Lancet 379 2012 2162 2172