Does immune reconstitution syndrome promote active tuberculosis in patients receiving highly active antiretroviral therapy?

被引:77
作者
Breen, RAM
Smith, CJ
Cropley, I
Johnson, MA
Lipman, MCI
机构
[1] UCL Royal Free Hosp, Dept Thorac & HIV Med, London NW3 2QG, England
[2] UCL Royal Free & Univ Coll Med Sch, Dept Primary Care & Populat Sci, London, England
关键词
tuberculosis; HIV infection; tuberculosis treatment; anti-retroviral therapy; immune reconstitution;
D O I
10.1097/01.aids.0000176221.33237.67
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objectives: To assess whether highly active anti-retroviral therapy (HAART) contributes to the presentation of active tuberculosis (TB). Design: Retrospective single-centre cohort study. Methods: A total of 111 HIV-infected individuals with active TB were identified at an urban teaching hospital between February 1997 and April 2004. Those receiving HAART at the time of TB diagnosis were assessed. Results: Nineteen of 111 (17%) were receiving HAART when TB developed. Within this group there appeared to be two distinct populations. Thirteen of 19, 12 from ethnic or social groups with high background rates of TB, developed disease a median of 41 days (range, 7-109) after starting HAART ('early TB' group). In six of 19 ('late TB' group), TB occurred a median of 358 days after HAART initiation (range, 258-598). The 'early TB' group had lower CD4 cell counts when starting HAART in comparison with the 'late TB' group (median; 87 versus 218 x 106 cells/l; P = 0.04); however no difference was observed in the rate of change of CD4 cell count (P = 0.5) or HIV load. Paradoxical reaction rate in the 'early TB' group was significantly greater than in the 'late-TB' group (62 versus 0%, P = 0.02) and greater than in a similar control population who started HAART while taking anti-TB therapy (62 versus 30%, P = 0.05). Conclusions: These data suggest anti-HIV treatment may amplify the presentation of active TB. This has implications for antiretroviral programmes in countries with high TB rates and warrants prospective investigation of a larger cohort. (c) 2005 Lippincott Williams & Wilkins.
引用
收藏
页码:1201 / 1206
页数:6
相关论文
共 21 条
[1]  
Barry S M, 2002, HIV Med, V3, P207, DOI 10.1046/j.1468-1293.2002.00115.x
[2]   Purified protein derivative-activated type 1 cytokine-producing CD4+ T lymphocytes in the lung:: A characteristic feature of active pulmonary and nonpulmonary tuberculosis [J].
Barry, SM ;
Lipman, MC ;
Bannister, B ;
Johnson, MA ;
Janossy, G .
JOURNAL OF INFECTIOUS DISEASES, 2003, 187 (02) :243-250
[3]   Paradoxical reactions during tuberculosis treatment in patients with and without HIV co-infection [J].
Breen, RAM ;
Smith, CJ ;
Bettinson, H ;
Dart, S ;
Bannister, B ;
Johnson, MA ;
Lipman, MCI .
THORAX, 2004, 59 (08) :704-707
[4]   Clinical indicators of immune restoration following highly active antiretroviral therapy [J].
Cooney, EL .
CLINICAL INFECTIOUS DISEASES, 2002, 34 (02) :224-233
[5]   The growing burden of tuberculosis - Global trends and interactions with the HIV epidemic [J].
Corbett, EL ;
Watt, CJ ;
Walker, N ;
Maher, D ;
Williams, BG ;
Raviglione, MC ;
Dye, C .
ARCHIVES OF INTERNAL MEDICINE, 2003, 163 (09) :1009-1021
[6]  
Girardi E, 2001, J ACQ IMMUN DEF SYND, V26, P326, DOI 10.1097/00126334-200104010-00006
[7]   Impact of combination antiretroviral therapy on the risk of tuberculosis among persons with HIV infection [J].
Girardi, E ;
Antonucci, G ;
Vanacore, P ;
Libanore, M ;
Errante, I ;
Matteelli, A ;
Ippolito, G .
AIDS, 2000, 14 (13) :1985-1991
[8]   Adult respiratory distress syndrome as a severe immune reconstitution disease following the commencement of highly active antiretroviral therapy [J].
Goldsack, NR ;
Allen, S ;
Lipman, MCI .
SEXUALLY TRANSMITTED INFECTIONS, 2003, 79 (04) :337-338
[9]   Latent tuberculosis infection [J].
Jasmer, RM ;
Nahid, P ;
Hopewell, PC .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 347 (23) :1860-1866
[10]   Human immunodeficiency virus type 1-related pulmonary Mycobacterium xenopi infection:: A need to treat? [J].
Kerbiriou, L ;
Ustianowski, A ;
Johnson, MA ;
Gillespie, SH ;
Miller, RF ;
Lipman, MCI .
CLINICAL INFECTIOUS DISEASES, 2003, 37 (09) :1250-1254