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Immunological memory, a pivotal pillar of the adaptive immune system, is responsible for the body's ability to remember and respond more swiftly and effectively to previously encountered pathogens. This remarkable feature is what makes vaccines so effective in preventing diseases.
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The T and B lymphocytes of the adaptive immune system develop from common lymphoid progenitor cells in the bone marrow. These progenitors give rise to precursors that eventually develop into both T and B lymphocytes. As these precursors mature, they gain the ability to detect and respond to foreign antigens in the body, a process known as immunocompetence. Additionally, these precursors acquire self-tolerance, a process that ensures they do not react to self-antigens. This intricate system...
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In the CNS, neurogenesis, the birth of new neurons from stem cells, is limited to the hippocampus in adults. In other regions of the brain and spinal cord, neurogenesis is almost non-existent due to inhibitory influences from neuroglia, especially oligodendrocytes, and the absence of growth-stimulating cues. The myelin produced by oligodendrocytes in the CNS inhibits neuronal regeneration. Furthermore, astrocytes proliferate rapidly after neuronal damage, forming scar tissue that physically...
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An inflammatory response is a localized, nonspecific immune reaction that occurs when a tissue is injured. It is characterized by redness, swelling, heat, and pain, which are commonly called the cardinal signs and symptoms of inflammation. Inflammation can sometimes result in a loss of function.
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Related Experiment Video

Updated: Oct 15, 2025

Strategies for Study of Neuroprotection from Cold-preconditioning
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Published on: September 2, 2010

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Cold exposure protects from neuroinflammation through immunologic reprogramming.

Martina Spiljar1, Karin Steinbach2, Dorothée Rigo1

  • 1Department of Cell Physiology and Metabolism, Faculty of Medicine, Centre Médical Universitaire (CMU), University of Geneva, Geneva, Switzerland; Diabetes Center, Faculty of Medicine, University of Geneva, Geneva, Switzerland.

Cell Metabolism
|October 23, 2021
PubMed
Summary
This summary is machine-generated.

Cold exposure ameliorates experimental autoimmune encephalomyelitis (EAE) by modulating monocytes, reducing T-cell priming. This suggests an energetic trade-off between cold adaptation and autoimmunity, benefiting immune-mediated diseases.

Keywords:
T cell primingautoimmunitybone marrowcold exposureexperimental autoimmune encephalomyelitisimmunometabolisminflammationmonocytesmultiple sclerosisneuroinflammation

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Area of Science:

  • Immunology
  • Neuroscience
  • Metabolic studies

Background:

  • Autoimmunity imposes significant metabolic costs.
  • The role of Ly6C-high monocytes in priming T cells in CNS autoimmunity is not fully understood.

Purpose of the Study:

  • To investigate the impact of cold exposure on immunity and immune-mediated diseases.
  • To elucidate the role of monocytes in cold-induced immune modulation during experimental autoimmune encephalomyelitis (EAE).

Main Methods:

  • Unbiased analysis of immune changes in various compartments during cold exposure in mouse models.
  • Assessment of monocyte MHCII expression, T-cell priming, and pathogenicity.
  • Monocyte depletion and adoptive transfer of T helper cells.

Main Results:

  • Cold exposure significantly ameliorates active EAE.
  • Cold exposure decreases monocyte MHCII expression and suppresses T-cell priming and pathogenicity.
  • Monocyte modulation is critical for the cold-induced protective effects.

Conclusions:

  • Environmental temperature influences neuroinflammation through monocyte modulation.
  • Cold-induced metabolic adaptations may compete with autoimmunity, offering a therapeutic benefit for immune-mediated diseases.