ASSOCIATION OF HUMAN FC-GAMMA-RIIA (CD32) POLYMORPHISM WITH SUSCEPTIBILITY TO AND SEVERITY OF MENINGOCOCCAL DISEASE

Citation
Ae. Platonov et al., ASSOCIATION OF HUMAN FC-GAMMA-RIIA (CD32) POLYMORPHISM WITH SUSCEPTIBILITY TO AND SEVERITY OF MENINGOCOCCAL DISEASE, Clinical infectious diseases, 27(4), 1998, pp. 746-750
Citations number
28
Categorie Soggetti
Infectious Diseases",Immunology,Microbiology
ISSN journal
10584838
Volume
27
Issue
4
Year of publication
1998
Pages
746 - 750
Database
ISI
SICI code
1058-4838(1998)27:4<746:AOHF(P>2.0.ZU;2-A
Abstract
Phagocytosis of bacteria constitutes an important defense mechanism ag ainst invasive bacterial diseases. Efficacy of phagocytosis by polymor phonuclear neutrophils is known to vary between allotypes of Fc gamma RIIa (a class of Fc receptors for immunoglobulins that is constitutive ly expressed on neutrophils). We compared the distribution of Fc gamma RIIa-R131 and Fc gamma RIIa-H131 allotypes in 98 Slavic complement-su fficient patients with meningococcal disease with that of the allotype s in 107 healthy controls. A strong association was found between the IIa-R/R131 allotype and the development of meningococcal disease after the age of 5 years, compared with IIa-R/H131 and IIa-H/H131 allotypes (P < .03; odds ratio [OR], 2.9), A severe course of meningococcal dis ease was observed in 21 (68%) of 31 episodes in patients with IIa-R/R1 31 genotype and in 22 (54%) of 41 episodes in patients with IIa-R/H131 genotype, in contrast to eight (31%) of 26 episodes in patients with IIa-H/H131 genotype (P < .02; OR, 4.7). Our data show that individuals older than 5 years of age who have the IIa-H/H131 allotype are less s usceptible to severe meningococcal disease than are individuals with t he IIa-R/R131 or IIa-R/H131 genotype.