The influence of FcγRIIa polymorphism on rheumatoid arthritis;Rola polimorfizmu FcγRIIa w przebiegu reumatoidalnego zapalenia stawów

Polskie Archiwum Medycyny Wewnetrznej

Volumn 112, Issue 2, 2004, Pages 907-910

  Pawlik, Andrzej ^a,c   Ostanek, Lidia ^b   Brzosko, Iwona ^b   Da̧browska Zamojcin, Ewa ^a   Brzosko, Marek ^b   Florczak, Marcin ^a   Gawrońska Szklarz, Barbara ^a  

^a AM   (Poland)

^b AM   (Poland)

^c Monitorowanej Pomorskiej   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

C REACTIVE PROTEIN; FC RECEPTOR; IMMUNOGLOBULIN G; FCGR2A PROTEIN, HUMAN;

ADULT; AGED; ANTIGEN ANTIBODY COMPLEX; ARTICLE; DISEASE ACTIVITY; ERYTHROCYTE SEDIMENTATION RATE; FEMALE; GENETIC POLYMORPHISM; HUMAN; MAJOR CLINICAL STUDY; MALE; RHEUMATOID ARTHRITIS; GENETICS; GENOTYPE; IMMUNOLOGY; METABOLISM; MIDDLE AGED;

ARTHRITIS, RHEUMATOID; C-REACTIVE PROTEIN; FEMALE; GENOTYPE; HUMANS; IMMUNOGLOBULIN G; MALE; MIDDLE AGED; POLYMORPHISM, GENETIC; RECEPTORS, IGG;

EID: 4944219600     PISSN: 00323772     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (12)

1. Rosenfeld S.I., Looney R.J., Leddy J.P., Phipps D.C., Abraham G.N., Anderson C.L.: Human platelet Fc receptor for immunoglobulin G. J. Clin. Invest., 1985, 76, 2317.
2. Parren P.W., Warmerdam P.A., Boeije L.C.: On the interaction of IgG subclasses with the low affinity FcγRIIa (CD32) on human monocytes, neutrophils, and platelets: analysis of a functional polymorphism to human IgG2. J. Clin. Invest., 1992, 90, 1537.
3. Warmerdam P.A., Van de Winkel J.G., Gosselin E.J., Capel P.J. : Molecular basis for a polymorphism of human Fcγ receptor II (CD32). J. Exp. Med., 1994, 172, 19.
4. Salmon J.E., Edberg J.C., Brogle N.L., Kimberley R.P.: Allelic polymorphisms of human Fcγ receptor IIA and Fcγ receptor IIIB. Independent mechanisms for differences in human phagocyte function. J. Clin. Invest., 1992, 89, 127.
5. Bredus R.G., Derkx B.H., Fijen C.A. i wsp.: Fcγ receptor IIa (CD32) polymorphism in fulminant meningococcal septic shock in children. J. Infect. Dis., 1994, 170, 848.
6. Nagata M., Hara T., Aoki T. i wsp.: Inherited deficiency of ninth component of complement an increased risk of meningococcal meningitis. J. Pediatr., 1989, 114, 260.
7. Duits A.J., Bootsma H., Derksen R.H.; Skewed distribution of IgGFc receptor IIa (CD32) polymorphism is associated with renal disease in systemic lupus erythematosus patients. Arthritis Rheum., 1995, 39, 1832.
8. Salmon J.E., Miliard S., Schachter L.A.: FcγRIIA alleles are heritable risk factors for lupus nephritis in African Americans. J. Clin. Invest., 1996, 97, 1348.
9. Carlsson L.E., Santoso S., Baurichter G. i wsp.: Heparin-induced thrombocytopenia: new insights into the impact of the FcγRIIa RH131 polymorphism. Blood, 1998, 92, 1526.
10. Burgess J.K., Lindeman R., Chesterman C.N., Chong B.H.: Single amino acid mutation of Fcγ receptor is associated with the development of heparin-induced thrombocytopenia. Br. J. Haematol., 1995, 91, 761.
11. Pawlik A., Ostanek L., Brzosko I. i wsp.: FcγRIIa polymorphism in patients with rheumatoid arthritis. Clin. Exp. Rheumatol., 2002, 20, 174.
12. Flesch B.K., Bauer F., Neppert J.: Rapid typing the human Fcγ receptor IIA polymorphism by polymerase chain reaction amplification with allele specific primers. Transfusion, 1998, 38, 174.