C-reactive protein – My perspective on its first half century, 1930-1982
C-reactive protein (CRP) was discovered in 1930 in the sera of patients during the acute phase of pneumococcal pneumonia and was so named because it bound to the C-polysaccharide of the pneumococcal cell wall. During the next half century many questions raised by this discovery were answered. Phosph...
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| Format: | Article |
| Language: | English |
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Frontiers Media S.A.
2023-03-01
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| Series: | Frontiers in Immunology |
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| Online Access: | https://www.frontiersin.org/articles/10.3389/fimmu.2023.1150103/full |
| _version_ | 1811161539162406912 |
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| author | Irving Kushner |
| author_facet | Irving Kushner |
| author_sort | Irving Kushner |
| collection | DOAJ |
| description | C-reactive protein (CRP) was discovered in 1930 in the sera of patients during the acute phase of pneumococcal pneumonia and was so named because it bound to the C-polysaccharide of the pneumococcal cell wall. During the next half century many questions raised by this discovery were answered. Phosphorylcholine was found to be the moiety of the C-polysaccharide to which CRP bound. The molecular structure of CRP was elucidated: five identical subunits arranged in cyclic symmetry, giving rise to the term pentraxin. Initially felt to be not normally present in the blood, CRP was found to be a component of normal serum in trace amounts. Its site of origin was determined to be the hepatocyte. It became clear that the presumed humoral mediator responsible for CRP induction was of leukocytic origin. Binding of CRP to its ligand activated the complement system, one of the important effector mechanisms of innate immunity. CRP was found to stimulate phagocytosis of some bacterial species via binding to Fc receptors and was found to be protective in vivo against the pneumococcus in mice. It appeared likely that a related function of CRP was clearance of necrotic tissue. CRP was recognized as being a highly evolutionary conserved molecule. Its discovery during the acute phase of pneumococcal pneumonia led to its being dubbed an acute phase protein. What we today call “the acute phase response”, refers to the large number of behavioral, physiologic, biochemical, and nutritional changes that occur during inflammatory states. |
| first_indexed | 2024-04-10T06:15:58Z |
| format | Article |
| id | doaj.art-409f724b11b04720a5008f8b9ba3fdfd |
| institution | Directory Open Access Journal |
| issn | 1664-3224 |
| language | English |
| last_indexed | 2024-04-10T06:15:58Z |
| publishDate | 2023-03-01 |
| publisher | Frontiers Media S.A. |
| record_format | Article |
| series | Frontiers in Immunology |
| spelling | doaj.art-409f724b11b04720a5008f8b9ba3fdfd2023-03-02T06:58:55ZengFrontiers Media S.A.Frontiers in Immunology1664-32242023-03-011410.3389/fimmu.2023.11501031150103C-reactive protein – My perspective on its first half century, 1930-1982Irving KushnerC-reactive protein (CRP) was discovered in 1930 in the sera of patients during the acute phase of pneumococcal pneumonia and was so named because it bound to the C-polysaccharide of the pneumococcal cell wall. During the next half century many questions raised by this discovery were answered. Phosphorylcholine was found to be the moiety of the C-polysaccharide to which CRP bound. The molecular structure of CRP was elucidated: five identical subunits arranged in cyclic symmetry, giving rise to the term pentraxin. Initially felt to be not normally present in the blood, CRP was found to be a component of normal serum in trace amounts. Its site of origin was determined to be the hepatocyte. It became clear that the presumed humoral mediator responsible for CRP induction was of leukocytic origin. Binding of CRP to its ligand activated the complement system, one of the important effector mechanisms of innate immunity. CRP was found to stimulate phagocytosis of some bacterial species via binding to Fc receptors and was found to be protective in vivo against the pneumococcus in mice. It appeared likely that a related function of CRP was clearance of necrotic tissue. CRP was recognized as being a highly evolutionary conserved molecule. Its discovery during the acute phase of pneumococcal pneumonia led to its being dubbed an acute phase protein. What we today call “the acute phase response”, refers to the large number of behavioral, physiologic, biochemical, and nutritional changes that occur during inflammatory states.https://www.frontiersin.org/articles/10.3389/fimmu.2023.1150103/fullC-reactive proteinacute phase responsecomplementphagocytosisRockefeller Institute |
| spellingShingle | Irving Kushner C-reactive protein – My perspective on its first half century, 1930-1982 Frontiers in Immunology C-reactive protein acute phase response complement phagocytosis Rockefeller Institute |
| title | C-reactive protein – My perspective on its first half century, 1930-1982 |
| title_full | C-reactive protein – My perspective on its first half century, 1930-1982 |
| title_fullStr | C-reactive protein – My perspective on its first half century, 1930-1982 |
| title_full_unstemmed | C-reactive protein – My perspective on its first half century, 1930-1982 |
| title_short | C-reactive protein – My perspective on its first half century, 1930-1982 |
| title_sort | c reactive protein my perspective on its first half century 1930 1982 |
| topic | C-reactive protein acute phase response complement phagocytosis Rockefeller Institute |
| url | https://www.frontiersin.org/articles/10.3389/fimmu.2023.1150103/full |
| work_keys_str_mv | AT irvingkushner creactiveproteinmyperspectiveonitsfirsthalfcentury19301982 |