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Drugs for Treatment of Crohn's Disease in IBD Using Biologic Agents: Anti-TNF01:24

Drugs for Treatment of Crohn's Disease in IBD Using Biologic Agents: Anti-TNF

Tumor Necrosis Factor (TNF), a proinflammatory cytokine, contributes significantly to the inflammation seen in Crohn's disease. It exists as soluble TNF and membrane-bound TNF, with actions mediated through TNF receptors (TNFR). TNFR activation leads to the release of proinflammatory cytokines, T-cell activation, collagen production, and leukocyte migration, all contributing to inflammation in Crohn's disease. Anti-TNF monoclonal antibodies, namely infliximab (Remicade), adalimumab (Humira),...
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Antibody Structure

Overview
Antibodies, also known as immunoglobulins (Ig), are essential players of the adaptive immune system. These antigen-binding proteins are produced by B cells and make up 20 percent of the total blood plasma by weight. In mammals, antibodies fall into five different classes, which each elicits a different biological response upon antigen binding.
The Y-Shaped Structure of Antibodies Consists of Four Polypeptide Chains
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Immunoglobulin-like Cell Adhesion Molecules

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Related Experiment Video

Updated: Jul 11, 2026

Induction of Experimental Autoimmune Encephalomyelitis in Mice and Evaluation of the Disease-dependent Distribution of Immune Cells in Various Tissues
08:47

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Published on: May 8, 2016

Anti-chemokine therapy for inflammatory diseases.

M L Castellani1, K Bhattacharya, M Tagen

  • 1Department of Internal Medicine and Science of Ageing, University of Chieti, Italy. mlcastellani@unich.it

International Journal of Immunopathology and Pharmacology
|September 21, 2007
PubMed
Summary
This summary is machine-generated.

Chemokines like CCL2/MCP-1 and CCL5/RANTES are key in inflammation. Inhibiting these chemokines shows promise for treating various diseases, including cancer and autoimmune disorders.

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Area of Science:

  • Immunology
  • Molecular Biology
  • Cell Biology

Background:

  • Chemokines are inflammatory proteins that signal through G-protein coupled receptors.
  • CCL2/MCP-1 and CCL5/RANTES are key CC chemokine subfamily members involved in inflammation.
  • These chemokines regulate inflammatory cell recruitment to tissues.

Purpose of the Study:

  • To explore the emerging roles of RANTES and MCP-1 in inflammation.
  • To investigate the therapeutic potential of inhibiting MCP-1 and RANTES.
  • To assess the utility of RANTES and MCP-1 as diagnostic and prognostic markers.

Main Methods:

  • Review of chemokine signaling pathways.
  • Analysis of the role of CC chemokines in inflammatory cell recruitment.
  • Evaluation of therapeutic strategies targeting MCP-1 and RANTES.

Main Results:

  • MCP-1 and RANTES play significant roles in inflammatory cell recruitment.
  • Inhibition of MCP-1 and RANTES demonstrates potential therapeutic benefits.
  • These chemokines may serve as valuable diagnostic and prognostic indicators.

Conclusions:

  • CCL2/MCP-1 and CCL5/RANTES are critical in inflammatory processes.
  • Targeting these chemokines offers therapeutic avenues for diverse diseases.
  • RANTES and MCP-1 hold potential for diagnostics and prognostics in various clinical conditions.