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Journal ArticleDOI

Neonatal adaptive immunity comes of age

TLDR
This review focuses on the new understanding in mice and, where it is clear that related phenomena occur, in humans.
Abstract
The past decade has brought great strides in our understanding of adaptive immunity in neonatal mice. Although poor immune responses are commonly observed, it is now clear that mature function can be achieved by all arms of the adaptive immune system. An ever-increasing body of evidence indicates that the neonatal period of life is a unique developmental stage in which responses are highly plastic and dependent on the conditions of antigen exposure. This review focuses on our new understanding in mice and, where it is clear that related phenomena occur, in humans.

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Adverse childhood experiences, allostasis, allostatic load, and age-related disease

TL;DR: Adverse childhood experiences induce significant biological changes in children (biological embedding), modifying the maturation and the operating balance of allostatic systems, and can exert long-term effects on biological aging and health.
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Innate immunity of the newborn: basic mechanisms and clinical correlates

TL;DR: Invention of innate immunity in newborns is described and how this knowledge might be used to prevent and treat infection in this vulnerable population is discussed.
Journal ArticleDOI

IgG Placental Transfer in Healthy and Pathological Pregnancies

TL;DR: There is evidence that IgG transfer depends on the following: (i) maternal levels of total IgG and specific antibodies, (ii) gestational age, (iii) placental integrity, (iv) IgG subclass, and (v) nature of antigen, being more intense for thymus-dependent ones.
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Respiratory Viral Infections in Infants: Causes, Clinical Symptoms, Virology, and Immunology

TL;DR: In this review, the complete picture from epidemiology and virology to clinical impact and immunology is explored, finding that both the virus and the immune response contribute to damage to the lungs and subsequent disease, and therefore, any prevention or treatment needs to address both of these factors.
Journal ArticleDOI

Macrophages are required for neonatal heart regeneration

TL;DR: It is suggested that macrophages provide necessary signals to drive angiogenesis and regeneration of the neonatal mouse heart, and modulating inflammation may provide a key therapeutic strategy to support heart regeneration.
References
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Journal ArticleDOI

A chemokine-driven positive feedback loop organizes lymphoid follicles

TL;DR: It is established that B-lymphocyte chemoattractant (BLC/BCA1) and its receptor, CXCR5, are needed for B-cell homing to follicles in lymph nodes as well as in spleen, and that BLC is required for the development of most lymph nodes and Peyer's patches.
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B cell development pathways.

TL;DR: Progress in understanding some aspects of this process in the mouse bone marrow is reviewed, focusing on delineation of the earliest stages of commitment, on pre-B cell receptor selection, and B cell tolerance during the immature-to-mature B cell transition.
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Mouse type I IFN-producing cells are immature APCs with plasmacytoid morphology.

TL;DR: It is shown that mouse interferon-α–producing cells (mIPCs) are a unique subset of immature antigen-presenting cells (APCs) that secrete IFN-α upon stimulation with viruses and interleukin 12 (IL-12) in response to viruses and CpG oligodeoxynucleotides, but not bacterial products.
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Marginal Zone and B1 B Cells Unite in the Early Response against T-Independent Blood-Borne Particulate Antigens

TL;DR: Splenic MZ and B1 B cells endowed with a "natural memory" provide a bridge between the very early innate and the later appearing adaptive immune response.
Journal ArticleDOI

Development of allergen-specific T-cell memory in atopic and normal children

TL;DR: The continuation of fetal allergen-specific Th2 responses during infancy is a defining feature of the inductive phase of atopic disease, and is associated with decreased capacity for production of the Th1 cytokine interferon y by atopic neonates.
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