Overturf Gary D
Department of Pediatrics and Pathology, Division of Pediatric Infectious Diseases, University of New Mexico Health Sciences Center, Albuquerque, NM 87131, USA.
Clin Infect Dis. 2003 Jan 15;36(2):189-94. doi: 10.1086/345527. Epub 2002 Dec 31.
Although people with bacterial meningitis lack adequate protective antibody against the invading pathogen, most do not have an underlying immunodeficiency. Certain comorbid conditions increase the risk for development of bacterial sepsis and meningitis. In addition, certain congenital complement deficiencies, defects of antibody production, or asplenia may be first recognized by the occurrence of bacterial meningitis, particularly when it occurs in infants or young children. Deficiencies of the terminal components of complement (C5-C9) or properdin have been associated with recurrent or invasive neisserial infections, and asplenia, agammaglobulinemia, and deficiencies of the early components of complement (e.g., C1-C3) are associated with risks of infections caused by Streptococcus pneumoniae, Haemophilus influenzae, and meningococci. The presence of congenital or acquired immunodeficiencies should be considered in persons who present with bacterial meningitis on the basis of the etiology, clinical epidemiology, and presence of other risk factors.
虽然患有细菌性脑膜炎的人缺乏针对入侵病原体的足够保护性抗体,但大多数人并没有潜在的免疫缺陷。某些合并症会增加发生细菌性败血症和脑膜炎的风险。此外,某些先天性补体缺陷、抗体产生缺陷或无脾症可能首先通过细菌性脑膜炎的发生而被发现,尤其是当它发生在婴儿或幼儿身上时。补体终末成分(C5-C9)或备解素的缺陷与复发性或侵袭性奈瑟菌感染有关,而无脾症、无丙种球蛋白血症和补体早期成分(如C1-C3)的缺陷与肺炎链球菌、流感嗜血杆菌和脑膜炎球菌引起的感染风险有关。根据病因、临床流行病学和其他危险因素的存在情况,对于患有细菌性脑膜炎的人,应考虑先天性或获得性免疫缺陷的存在。