Bakken Johan S, Haller Irina, Riddell Debbie, Walls Jennifer J, Dumler J Stephen
Section of Infectious Diseases, St. Mary Duluth Clinic Health System, Duluth, MN 55805, USA.
Clin Infect Dis. 2002 Jan 1;34(1):22-7. doi: 10.1086/323811. Epub 2001 Nov 21.
To characterize the serological response in humans to human granulocytic ehrlichiosis (HGE), we prospectively observed 152 patients for as long as 42 months. HGE was confirmed by detection of morulae in blood smears, polymerase chain reaction, blood culture, or a combination of these tests for 94 patients (62.3%), and 92 (97.8%) of the patients had specific serum antibodies thereafter. One hundred twenty-six (99.2%) of 127 patients tested at 1 month were seropositive (89 of 127 patients had seroconversion), and 150 (98.7%) of the 152 patients had become seropositive by 6 months. Eleven patients (7.3%) remained seropositive at 42 months. Neither antibiotic therapy initiated during the first week of illness nor preexisting immunosuppressive conditions abrogated a serological response. Indirect fluorescent antibody testing of acute-phase and convalescent-phase serum samples is a sensitive tool for laboratory confirmation of HGE.
为了描述人类对人粒细胞埃立克体病(HGE)的血清学反应,我们前瞻性地观察了152例患者长达42个月。通过在血涂片、聚合酶链反应、血培养或这些检测方法的组合中检测桑葚体,确诊94例(62.3%)患者患有HGE,此后92例(97.8%)患者产生了特异性血清抗体。127例在1个月时接受检测的患者中有126例(99.2%)血清呈阳性(127例患者中有89例发生血清转化),152例患者中有150例(98.7%)在6个月时血清呈阳性。11例患者(7.3%)在42个月时仍血清呈阳性。在疾病第一周开始的抗生素治疗和既往存在的免疫抑制状况均未消除血清学反应。急性期和恢复期血清样本的间接荧光抗体检测是实验室确诊HGE的敏感工具。