Incidence and risk factors for the immune reconstitution inflammatory syndrome in HIV patients in South Africa: a prospective study

被引:214
作者
Murdoch, David M. [1 ]
Venter, Willem D. F. [2 ]
Feldman, Charles [3 ]
Van Rie, Annelies [4 ]
机构
[1] Duke Univ, Med Ctr, Div Pulm & Crit Care Med, Durham, NC 27710 USA
[2] Univ Witwatersrand, Reprod Hlth & HIV Res Unit, Johannesburg, South Africa
[3] Univ Witwatersrand, Div Pulm, Dept Med, Johannesburg Hosp, Johannesburg, South Africa
[4] Univ N Carolina, Dept Epidemiol, Chapel Hill, NC USA
关键词
HIV; immune reconstitution inflammatory syndrome; incidence; IRIS; opportunistic infections; risk factors; sub-Saharan Africa;
D O I
10.1097/QAD.0b013e3282f4a607
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: To determine the incidence, clinical manifestations, risk factors and outcome of immune reconstitution inflammatory syndrome (IRIS) in South Africa. Design: Prospective surveillance cohort and nested case-control study in a large, University hospital-based antiretroviral therapy (ART) clinic. Methods: A total of 423 ART-naive HIV-infected South African patients were followed for signs and symptoms IRIS during the first 6 months of ART. We also performed a nested case-control study with controls matched to IRIS cases on ART duration. Results: During the first 6 months of ART, 44 (10.4%) patients experienced IRIS for an overall incidence rate of 25.1 cases per 100 patient-years. Diagnoses included tuberculosis (18/44, 41%), abscess formation and suppurative folliculitis (8/44, 18.2%), varicella zoster (6/44, 13.6%), herpes simplex (4/44, 9.1%), cryptococcal meningitis (3/44, 6.8%), molluscum contagiosum (3/44, 6.8%), and Kaposi's sarcoma (2/44, 4.5%). Median IRIS onset was 48 days (interquartile range, 29-99) from ART initiation. In comparison with controls, IRIS cases had significantly lower CD4 cell counts at baseline (79 versus 142 cells/mu l; P= 0.02) and at IRIS diagnosis (183 versus 263 cells/mu l; P= 0.05), but similar virological and immunological response to ART. In multivariable analyses, higher baseline CD4 cell count was protective of developing IRIS (HR 0.72 per 50 cells/mu l increase). Most IRIS cases were mild, with ART discontinued in three (6.8%) patients, corticosteroids administered to four (9.1%) patients, and hospitalization required in 12 (27.3%) patients. Two deaths were attributable to IRIS. Conclusions: IRIS may affect 10% of patients initiating ART in Africa, particularly those with advanced immunosuppression, but severe, life-threatening IRIS is uncommon. (C) 2008 Wolters Kluwer Health Lippincott Williams & Wilkins.
引用
收藏
页码:601 / 610
页数:10
相关论文
共 27 条
[1]   Explosion of tuberculin-specific Th1-responses induces immune restoration syndrome in tuberculosis and HIV co-infected patients [J].
Bourgarit, A ;
Carcelain, G ;
Martinez, V ;
Lascoux, C ;
Delcey, V ;
Gicquel, B ;
Vicaut, E ;
Lagrange, PH ;
Sereni, D ;
Autran, B .
AIDS, 2006, 20 (02) :F1-F7
[2]   Determinants of immune reconstitution inflammatory syndrome in HIV type 1 -: Infected patients with tuberculosis after initiation of antiretroviral therapy [J].
Breton, G ;
Duval, X ;
Estellat, C ;
Poaletti, X ;
Bonnet, D ;
Mvondo, DM ;
Longuet, P ;
Leport, C ;
Vildé, JL .
CLINICAL INFECTIOUS DISEASES, 2004, 39 (11) :1709-1712
[3]   Initial increase in blood CD4+ lymphocytes after HIV antiretroviral therapy reflects redistribution from lymphoid tissues [J].
Bucy, RP ;
Hockett, RD ;
Derdeyn, CA ;
Saag, MS ;
Squires, K ;
Sillers, M ;
Mitsuyasu, RT ;
Kilby, JM .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (10) :1391-1398
[4]  
ELLIOTT JH, 2007, 4 IAS C HIV PATH TRE
[5]   Pulmonary tuberculosis in AIDS patients: Transient chest radiographic worsening after initiation of antiretroviral therapy [J].
Fishman, JE ;
Saraf-Lavi, E ;
Narita, M ;
Hollender, ES ;
Ramsinghani, R ;
Ashkin, D .
AMERICAN JOURNAL OF ROENTGENOLOGY, 2000, 174 (01) :43-49
[6]  
French M A, 2000, HIV Med, V1, P107, DOI 10.1046/j.1468-1293.2000.00012.x
[7]   Immune restoration disease after antiretroviral therapy [J].
French, MA ;
Price, P ;
Stone, SF .
AIDS, 2004, 18 (12) :1615-1627
[8]  
Gea-Banacloche JC, 1999, AIDS, V13, pS25
[9]   Cytomegalovirus retinitis after initiation of highly active antiretroviral therapy [J].
Jacobson, MA ;
Zegans, M ;
Pavan, PR ;
ODonnell, JJ ;
Sattler, F ;
Rao, N ;
Owens, S ;
Pollard, R .
LANCET, 1997, 349 (9063) :1443-1445
[10]   The prevalence and risk of immune restoration disease in HIV-infected patients treated with highly active antiretroviral therapy [J].
Jevtovic, D ;
Salemovic, D ;
Ranin, J ;
Pesic, I ;
Zerjav, S ;
Djurkovic-Djakovic, O .
HIV MEDICINE, 2005, 6 (02) :140-143