Goddard E A, Beatty D W, Hoffman E B
Department of Pediatrics, University of Cape Town South
Pediatr Infect Dis J. 1996 May;15(5):419-24. doi: 10.1097/00006454-199605000-00008.
The purpose of this study was to determine whether the G2m(n), G1m(f) and Km(3) immunoglobulin allotypes have any association with susceptibility to invasive Haemophilus influenzae type b (Hib) and Staphylococcus aureus (S. aureus) infections in children.
Direct enzyme-linked immunosorbent assays with commercially available monoclonal antibodies were established to quantitate G2m(n) and G1m(f) allotypes. A qualitative enzyme-linked immunosorbent assay with polyclonal rabbit anti-Km(3) antibody was established for Km(3) determination.
The G2m(n) marker occurred in 34.4% of the mixed ancestry population and 2.9% of the Black population. There was a significantly decreased frequency of the G2m(n) allotype in mixed ancestry children with Hib meningitis (8.5%) and Hib osteomyelitis/septic arthritis and a decreased frequency of Km(3) in black and mixed ancestry children with Hib meningitis. The frequency of G2m(n), G1m(f) and Km(3) allotypes in patients with S. aureus osteomyelitis/septic arthritis were not significantly different from normal population frequency.
This study shows a clear association between the absence of the G2m(n) allotype in mixed ancestry children and susceptibility to invasive infections caused by H. influenzae and an association between the absence of Km(3) and Hib meningitis in both black and mixed ancestry children.
本研究旨在确定G2m(n)、G1m(f)和Km(3)免疫球蛋白同种异型是否与儿童侵袭性b型流感嗜血杆菌(Hib)和金黄色葡萄球菌(S. aureus)感染的易感性相关。
建立了使用市售单克隆抗体的直接酶联免疫吸附测定法来定量G2m(n)和G1m(f)同种异型。建立了使用多克隆兔抗Km(3)抗体的定性酶联免疫吸附测定法来测定Km(3)。
G2m(n)标记出现在34.4%的混合血统人群和2.9%的黑人人群中。患有Hib脑膜炎的混合血统儿童(8.5%)以及患有Hib骨髓炎/化脓性关节炎的混合血统儿童中G2m(n)同种异型的频率显著降低,患有Hib脑膜炎的黑人和混合血统儿童中Km(3)的频率降低。金黄色葡萄球菌骨髓炎/化脓性关节炎患者中G2m(n)、G1m(f)和Km(3)同种异型的频率与正常人群频率无显著差异。
本研究表明,混合血统儿童中缺乏G2m(n)同种异型与流感嗜血杆菌引起的侵袭性感染易感性之间存在明显关联,并且在黑人和混合血统儿童中,缺乏Km(3)与Hib脑膜炎之间存在关联。