TY - JOUR
T1 - Structured treatment interruptions following immediate initiation of HAART in eight patients with acute HIV-1 seroconversion
AU - Vogel, M.
AU - Lichterfeld, M.
AU - Kaufmann, D. E.
AU - Mui, S. K.
AU - Altfeld, M.
AU - Voigt, E.
AU - Ahlenstiel, G.
AU - Kupfer, B.
AU - Walker, B.
AU - Spengler, U.
AU - Rockstroh, Jürgen K.
PY - 2006/7/31
Y1 - 2006/7/31
N2 - Background: The immunological and clinical benefits of structured treatment interruptions (STIs) during primary HIV-1 infection remain largely unclear. Patients and Methods: Eight patients identified during primary HIV-1 infection were immediately treated with HAART and underwent subsequent STIs after reaching complete viral suppression of HIV-RNA in peripheral plasma. HAART was re-initiated if either HIV-1 RNA >5000 copies/ml, CD4-cells <200 cells/μl or symptomatic HIV-1 disease was observed. Results: After treatment discontinuation, four of eight patients were able to persistenily control HIV-1 viremia below 5000 copies/ml until the last time point of follow-up (median 3 years). CD4-cell counts were within the interquartile range of untreated individuals compared to historical reference data from the MACS cohort. In the remaining study subjects persistent virological control was not reached despite repeated STIs. Moreover, compared to the MACS cohort repetitive virological failures during STIs appeared to induce an accelerated decline of CD4-cells. Conclusion: Spontaneous HIV-1 control after treated primary HIV-1 infection was possible in four out of eight individuals, however, if STIs after treated primary infection ameliorate the overall HIV-1 disease progression remains unknown. In the absence of viral control, repetitive viral exposure during STIs might be associated with accelerated decline of CD4-cell counts.
AB - Background: The immunological and clinical benefits of structured treatment interruptions (STIs) during primary HIV-1 infection remain largely unclear. Patients and Methods: Eight patients identified during primary HIV-1 infection were immediately treated with HAART and underwent subsequent STIs after reaching complete viral suppression of HIV-RNA in peripheral plasma. HAART was re-initiated if either HIV-1 RNA >5000 copies/ml, CD4-cells <200 cells/μl or symptomatic HIV-1 disease was observed. Results: After treatment discontinuation, four of eight patients were able to persistenily control HIV-1 viremia below 5000 copies/ml until the last time point of follow-up (median 3 years). CD4-cell counts were within the interquartile range of untreated individuals compared to historical reference data from the MACS cohort. In the remaining study subjects persistent virological control was not reached despite repeated STIs. Moreover, compared to the MACS cohort repetitive virological failures during STIs appeared to induce an accelerated decline of CD4-cells. Conclusion: Spontaneous HIV-1 control after treated primary HIV-1 infection was possible in four out of eight individuals, however, if STIs after treated primary infection ameliorate the overall HIV-1 disease progression remains unknown. In the absence of viral control, repetitive viral exposure during STIs might be associated with accelerated decline of CD4-cell counts.
KW - HAART
KW - HIV-1
KW - Investigational therapies
KW - Primary HIV-1 infection
KW - Structured treatment interruption
UR - http://www.scopus.com/inward/record.url?scp=33747226141&partnerID=8YFLogxK
M3 - Article
C2 - 16899420
AN - SCOPUS:33747226141
SN - 0949-2321
VL - 11
SP - 273
EP - 278
JO - European Journal of Medical Research
JF - European Journal of Medical Research
IS - 7
ER -