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  Published Paper Details:

  Paper Title

BIOCHEMISTRY & PATHOPHYSIOLOGY OF C-REACTIVE PROTEIN [CRP]: A SIGNAL TO LIFE FROM THREAT

  Authors

  Dr. Deepak Kumar,  Supradip Mandal,  Arpita Biswas,  Dr. Dhrubo Jyoti Sen,  Dr. Dhananjoy Saha

  Keywords

Interleukin, Inflammation, Arthritis, Systemic Lupus Erythematosus, Apoptotic cell, Phospholipids, Macrophage, Adipocytes, Polysaccharide

  Abstract


C-reactive protein (CRP) was discovered by Tillett and Francis in 1930. The name CRP arose because it was first identified as a substance in the serum of patients with acute inflammation that reacted with the "c" carbohydrate antigen of the capsule of pneumococcus. CRP is a pentameric protein synthesized by the liver, whose level rises in response to inflammation. CRP is an acute-phase reactant protein that is primarily induced by the IL-6 action on the gene responsible for the transcription of CRP during the acute phase of an inflammatory/infectious process. There is some question about whether deregulation of the role of CRP in the clearance of apoptotic cells and cellular debris plays a role in the pathogenesis of systemic lupus erythematosus (SLE), but this has not been definitively demonstrated. It has been demonstrated to have some protective properties in animal studies on lung tissue in alveolitis by reducing neutrophil-mediated damage to the alveoli and protein leakage into the lung. CRP has both proinflammatory and anti-inflammatory properties. It plays a role in the recognition and clearance of foreign pathogens and damaged cells by binding to phosphocholine, phospholipids, histone, chromatin, and fibronectin. It can activate the classic complement pathway and also activate phagocytic cells via Fc receptors to expedite the removal of cellular debris and damaged or apoptotic cells and foreign pathogens. This can become pathologic, however, when it is activated by autoantibodies displaying the phosphocholine arm in auto-immune processes, such as idiopathic thrombocytopenic purpura (ITP). It can also worsen tissue damage in certain cases by activation of the complement system and thus inflammatory cytokines. As compared to the erythrocyte sedimentation rate, which is an indirect test for inflammation, the levels of CRP rise and fall rapidly with the onset and removal of the inflammatory stimulus, respectively. Persistently elevated CRP levels can be seen in chronic inflammatory conditions such as chronic infections or inflammatory arthritides such as rheumatoid arthritis. There are numerous causes of an elevated C-reactive protein. These include acute and chronic conditions, and these can be infectious or non-infectious in etiology. However, markedly elevated levels of CRP are most often associated with an infectious cause (an example of pathogen-associated molecular pattern recognition). Trauma can also cause elevations in CRP (alarming response). More modest elevations tend to be associated with a broader spectrum of etiologies, ranging from sleep disturbances to periodontal disease.

  IJCRT's Publication Details

  Unique Identification Number - IJCRT2209256

  Paper ID - 225572

  Page Number(s) - c1-c16

  Pubished in - Volume 10 | Issue 9 | September 2022

  DOI (Digital Object Identifier) -   

  Publisher Name - IJCRT | www.ijcrt.org | ISSN : 2320-2882

  E-ISSN Number - 2320-2882

  Cite this article

  Dr. Deepak Kumar,  Supradip Mandal,  Arpita Biswas,  Dr. Dhrubo Jyoti Sen,  Dr. Dhananjoy Saha,   "BIOCHEMISTRY & PATHOPHYSIOLOGY OF C-REACTIVE PROTEIN [CRP]: A SIGNAL TO LIFE FROM THREAT", International Journal of Creative Research Thoughts (IJCRT), ISSN:2320-2882, Volume.10, Issue 9, pp.c1-c16, September 2022, Available at :http://www.ijcrt.org/papers/IJCRT2209256.pdf

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