期刊论文详细信息
European Journal of Medical Research
Treatment during primary HIV infection does not lower viral set point but improves CD4 lymphocytes in an observational cohort
H Jaeger4  H Knechten6  A Goetzenich1  J Goelz1  M Rausch5  K Schewe2  H Jessen7  N Hanhoff1  E Wolf3  C Koegl3 
[1]DAGNAE e.V., Berlin, Germany
[2]IPM/ICH-Studycenter, Hamburg, Berlin
[3] Germany
[4]MUC Research, Munich, Germany
[5]MVZ Karlsplatz -HIV Research and Clinical Care Centre Munich, Munich, Germany
[6]Private Practice, Berlin
[7] Germany
[8]PZB Aachen, Germany
[9]HIV outpatient practice, Berlin, Germany
关键词: viral set point;    HIV;    antiretroviral therapy;    CD4 lymphocytes;    Primary HIV Infection;   
Others  :  1093692
DOI  :  10.1186/2047-783X-14-7-277
 received in 2008-12-17, accepted in 2009-06-02,  发布年份 2009
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【 摘 要 】

Objective

To investigate if early treatment of primary HIV-1 infection (PHI) reduces viral set point and/or increases CD4 lymphocytes.

Methods

Analysis of two prospective multi-centre PHI cohorts. HIV-1 RNA and CD4 lymphocytes in patients with transient treatment were compared to those in untreated patients. Time to CD4 lymphocyte decrease below 350/μl after treatment stop or seroconversion was calculated using Kaplan-Meier and Cox-PH-regression analyses.

Results

156 cases of PHI were included, of which 100 had received transient HAART (median treatment time 9.5 months) and 56 remained untreated. Median viral load (563000 cop/ml vs 240000 cop/ml; p < 0.001) and median CD4 lymphocyte (449/μl vs. 613/μl; p < 0.01) differed significantly between treated and untreated patients. Median viral load was 38056 copies/ml in treated patients (12 months after treatment stop) and 52880 copies/ml in untreated patients (12 months after seroconversion; ns). Median CD4 lymphocyte change was +60/μl vs. -86/μl (p = 0.01). Median time until CD4 lymphocytes decreased to < 350/μl (including all patients with CD4 lymphocytes < 500/μl during seroconversion) was 20.7 months in treated patients after treatment stop and 8.3 months in untreated patents after seroconversion (p < 0.01). Cox-PH analyses adjusting for baseline VL, CD4 lymphocytes, stage of early infection and symptoms confirmed these differences.

Conclusions

Treatment during PHI did not lower viral set point. However, patients treated during seroconversion had an increase in CD4 lymphocytes, whereas untreated patients experienced a decrease in CD4 lymphocytes. Time until reaching CD4 lymphocytes < 350/μl was significantly shorter in untreated than in treated patients including patients with CD4 lymphocytes < 500/μl during seroconversion.

【 授权许可】

   
2009 I. Holzapfel Publishers

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【 参考文献 】
  • [1]Gulick RM, Mellors JW, Havlir D, Eron JJ, Gonzalez C, McMahon D, et al.: Treatment with indinavir, zidovudine, and lamivudine in adults with human immunodeficiency virus infection and prior antiretroviral therapy. N Engl J Med 1997, 337:734-739.
  • [2]Musey L, Hughes J, Schacker T, Shea T, Corey L, McElrath MG: Cytotoxic-T-cell responses, viral load and disease progression in early human immunodeficiency virus type 1 infection. N Engl J Med 1997, 337:1267-1274.
  • [3]Farzadegan H, Henrard DR, Kleeberger CA, Schrager L, Kirby AJ, Saah AJ, et al.: Virologic and serologic markers of rapid progression to AIDS after HIV-1 seroconversion. J Acquir Immune Defic Syndr Hum Retrovirol 1996, 13:448-455.
  • [4]Blattner WA, Oursler KA, Cleghorn F, Charurat M, Sill A, Bartholomew C, et al.: Rapid clearance of virus after acute HIV-1 infection: correlates of risk of AIDS. J Infect Dis 2004, 189:1793-1801.
  • [5]Rosenberg ES, Altfeld M, Poon SH, Phillips MN, Wilkes BM, Eldridge RL, et al.: Immune control of HIV-1 after early treatment of acute infection. Nature 2000, 407:523-526.
  • [6]Oxenius A, Price DA, Easterbrook PJ, et al.: Early highly active antiretroviral therapy for acute HIV-1 infection preserves immune function of CD8+ and CD4+ T lymphocytes. Proc Natl Acad Sci USA 2000, 97:3382-3387.
  • [7]Jansen CA, De Cuyper IM, Steingrover R, Jurriaans S, Sankatsing SU, Prins JM, et al.: Analysis of the effect of highly active antiretroviral therapy during acute HIV-1 infection on HIV-1 specific CD4 T-cell functions. AIDS 2005, 11:1145-1154.
  • [8]Lisziewicz J, Rosenberg E, Lieberman J, Jessen H, Lopalco L, Silicano R, et al.: Control of HIV despite the discontinuation of antiretroviral therapy. N Engl J Med 1999, 340(21):1683-1684.
  • [9]Kinloch-De Loes S, Hirschel BJ, Hoen B, Cooper DA, Tindall B, Carr A, et al.: A controlled trial of zidovudine in primary human immunodeficiency virus infection. N Engl J Med 1995, 333:408-413.
  • [10]Niu MT, Bethel J, Holodniy M, Standiford HC, Schnittman SM: Zidovudine treatment in patients with primary (acute) human immunodeficiency virus type 1 infection: a randomized, double-blind, placebo-controlled trial. DATRI 002 Study Group. Division of AIDS Treatment Research Initiative. J Infect Dis 1998, 14:397-403.
  • [11]Smith DE, Walker BD, Cooper DA, Rosenberg ES, Kaldor JM: Is antiretroviral treatment of primary HIV infection clinically justified on the basis of current evidence? AIDS 2004, 18:709-718.
  • [12]Sterling TR, Chaisson RE, Keruly J, Moore RD: Improved outcomes with earlier initiation of highly active antiretroviral therapy among human immunodeficiency virus-infected patients who achieve durable virological suppression: longer follow-up of an observational cohort study. J Infect Dis 2003, 188:1659-1665.
  • [13]Kinloch-de Loes S: Treatment of acute HIV-1 infection: is it coming of age? J Infect Dis 2006, 194:721-724.
  • [14]Berrey MM, Schaker T, Collier AC, et al.: Treatment of primary human immunodeficiency virus type 1 infection with potent antiretroviral therapy reduces frequency of rapid progression to AIDS. J Infect Dis 2001, 183:1466-1475.
  • [15]Lindback S, Vizzard J, Cooper DA, Gaines H: Long-term prognosis following zidovudine monotherapy in primary human immunodeficiency virus type 1 infection. J Infect Dis 1999, 179:1549-1552.
  • [16]Girard PM, Schneider V, Dehee A, Mariot P, Jacomet C, Delphin N, et al.: Treatment interruption after one year of triple nucleoside analogue therapy for primary HIV infection. AIDS 2001, 15:275-277.
  • [17]Kaufmann DE, Lichterfeld M, Altfeld M, Addo MM, Johnston MN, Lee PK, et al.: Limited durability of viral control following treated acute HIV infection. PloS Med 2004, 1:e36.
  • [18]Markowitz M, Jin X, Hurley A, Simon V, Ramratnam B, Louie M, et al.: Discontinuation of antiretroviral therapy commenced early during the course of human immunodeficiency virus type 1 infection, with or without adjunctive vaccination. J Infect Dis 2002, 186:634-643.
  • [19]Fidler S, Oxenius A, Brady M, Clarke J, Cropley I, Babiker A, et al.: Virological and immunological effects of short-course antiretroviral therapy in primary HIV infection. AIDS 2002, 16:2049-2054.
  • [20]Lyles RH, Munoz A, Yamashita TE, Bazmi H, Detels R, Rinaldo CR, et al.: Natural history of human immunodeficiency virus type 1 viremia after seroconversion and proximal to AIDS in a large cohort of homosexual men. Multicenter AIDS Cohort Study. J Infect Dis 2000, 181:872-880.
  • [21]Cascade: Time from HIV-1 seroconversion to AIDS and death before widespread use of highly-active antiretroviral therapy: a collaborative re-analysis. Collaborative Group on AIDS Incubation and HIV Survival including the CASCADE EU Concerted Action. Concerted Action on SeroConversion to AIDS and Death in Europe. Lancet 2000, 355:1131-1137.
  • [22]Desquilbet L, Goujard C, Rouzioux C, Sinet M, Deveau C, Pellegrin I, for the PRIMO and SEROCO Study Groups: Does transient HAART during primary infection lower the virological set-point? AIDS 2004, 18:2361-2369.
  • [23]Hecht FM, Wang L, Collier A, Little S, Markowitz M, Margolock J, et al.: A multicenter observational study of the potential benefits of initiating combination antiretroviral therapy during acute HIV infection. J Infect Dis 2006, 194:725-733.
  • [24]Fidler S, Fox J, Touloumi G, Pantazis N, Porter K, Babiker A, the CASCADE Collaboration, et al.: Slower CD4 Cell Decline Following Cessation of a 3 Month Course of HAART in Primary HIV Infection: Findings From an Observational Cohort. AIDS 2007, 21(10):1283-1291.
  • [25]Fidler S, Fraser C, Fox J, Tamm N, Griffin JT, Weber J: Comparative potency of three antiretroviral therapy regimes in primary HIV infection. AIDS 2006, 20:247-252.
  • [26]CASCADE Collaboration: Changes in the uptake of antiretroviral therapy and survival in persons with known duration of HIV infection in Europe. HIV Med 2000, 1:224-231.
  • [27]Pantazis N, Touloumi G, Vanhems P, Gill J, Bucher HC, Porter K: The effect of antiretroviral treatment of different durations in primary HIV infection. AIDS 2008, 22:2441-2450.
  • [28]Seng R, Goujard C, Desquilbet L, Sinet M, Rouzioux C, Deveau C, et al.: Rapid CD4+ cell decrease after transient cART initiated during primary HIV infection (ANRS PRIMO and SEROCO cohorts). J Acquir Immune Defic Syndr 2008, 49(3):251-258.
  • [29]Clumeck N, Pozniak A, Raffi F: European AIDS Clinical Society (EACS) guidelines for the clinical management and treatment of HIV-infected adults. HIV Med 2008, 9:65-71.
  • [30]Fidler S, Fox J, Porter K, Weber J: Primary HIV infection: to treat or not to treat? Curr Opin Infect Dis 2008, 21:4-10.
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