Exogenous reinfection as a cause of recurrent tuberculosis after curative treatment

被引:467
作者
Van Rie, A
Warren, R
Richardson, M
Victor, TC
Gie, RP
Enarson, DA
Beyers, N
van Helden, PD
机构
[1] Univ Stellenbosch, Dept Pediat & Child Hlth, ZA-7505 Tygerberg, South Africa
[2] Univ Stellenbosch, MRC, Ctr Cellular & Mol Biol, ZA-7505 Tygerberg, South Africa
[3] Univ Stellenbosch, Dept Biochem Med, ZA-7505 Tygerberg, South Africa
[4] Katholieke Univ Leuven, Dept Pediat, Louvain, Belgium
关键词
D O I
10.1056/NEJM199910143411602
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background For decades it has been assumed that postprimary tuberculosis is usually caused by reactivation of endogenous infection rather than by a new, exogenous infection. Methods We performed DNA fingerprinting with restriction-fragment-length polymorphism analysis on pairs of isolates of Mycobacterium tuberculosis from 16 compliant patients who had a relapse of pulmonary tuberculosis after curative treatment of post-primary tuberculosis. The patients lived in areas of South Africa where tuberculosis is endemic. Medical records were reviewed for clinical data. Results For 12 of the 16 patients, the restriction-fragment-length polymorphism banding patterns for the isolates obtained after the relapse were different from those for the isolates from the initial tuberculous disease. This finding indicates that reinfection was the cause of the recurrence of tuberculosis after curative treatment. Two patients had reinfections with a multidrug-resistant strain. All 15 patients who were tested for the human immunodeficiency virus were seronegative. Conclusions Exogenous reinfection appears to be a major cause of postprimary tuberculosis after a previous cure in an area with a high incidence of this disease. This finding emphasizes the importance of achieving cures and of preventing anyone with infectious tuberculosis from exposing others to the disease. (N Engl J Med 1999;341:1174-9.) (C)1999, Massachusetts Medical Society.
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页码:1174 / 1179
页数:6
相关论文
共 15 条
[1]  
ALLAN WGL, 1982, TUBERCLE, V63, P89
[2]  
ALLAN WGL, 1977, AM REV RESPIR DIS, V115, P727
[3]  
Beyers N, 1996, S AFR MED J, V86, P40
[4]  
BRITISH THORACIC ASSOCIATION, 1982, American Review of Respiratory Disease, V126, P460
[5]  
CANETTI G, 1972, Bulletin of the International Union Against Tuberculosis, V47, P116
[6]  
DAS S, 1993, TUBERCLE LUNG DIS, V74, P48
[7]  
KATZ HL, 1958, VETERANS ADM ARMED F, P214
[8]  
MCKINNEY JD, 1997, PERSISTING PROBLEMS, P69
[9]   QUALITY-CONTROL IN TUBERCULOSIS BACTERIOLOGY .2. THE ORIGIN OF ISOLATED POSITIVE CULTURES FROM THE SPUTUM OF PATIENTS IN 4 STUDIES OF SHORT COURSE CHEMOTHERAPY IN AFRICA [J].
MITCHISON, DA ;
KEYES, AB ;
EDWARDS, EA ;
AYUMA, P ;
BYFIELD, SP ;
NUNN, AJ .
TUBERCLE, 1980, 61 (03) :135-144
[10]   RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISM TYPING OF CLINICAL ISOLATES OF MYCOBACTERIUM-TUBERCULOSIS FROM PATIENTS WITH PULMONARY TUBERCULOSIS IN MADRAS, INDIA, BY USE OF DIRECT-REPEAT PROBE [J].
SAHADEVAN, R ;
NARAYANAN, S ;
PARAMASIVAN, CN ;
PRABHAKAR, R ;
NARAYANAN, PR .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (11) :3037-3039