Low-dose IL-2 reduces lymphocyte apoptosis and increases naive CD4 cells in HIV-1 patients treated with HAART
- PMID: 10692234
- DOI: 10.1006/clim.2000.4837
Low-dose IL-2 reduces lymphocyte apoptosis and increases naive CD4 cells in HIV-1 patients treated with HAART
Abstract
During HIV disease an increased in vitro apoptosis of peripheral blood mononuclear cells has been demonstrated. This can be reversed in vitro by interleukin (IL)-2. Recent trials with highly active antiretroviral therapy (HAART) and IL-2 in HIV-1-infected patients showed promising immunological and clinical results. Here we investigated the effects of subcutaneous low-dose IL-2 administration in combination with HAART on in vitro apoptosis and the relationship between apoptosis, CD4(+) counts, and HIV replication. Twenty-two asymptomatic HIV patients were randomized for HAART (arm I) and HAART plus IL-2 (arm II). Spontaneous apoptosis was decreased in both arms after 28 weeks of therapy but the reduction was highly significant only in arm II (P = 0.05 vs P = 0.001). As the percentage of apoptosis decreased, there was a significantly higher increase of both CD4(+) and CD4(+) naive T cells in arm II vs arm I. HIV plasma viremia was reduced in all patients after therapy. Our data suggest that intermittent therapy with low-dose subcutaneous IL-2 in addition to HAART induces a positive immunomodulation in asymptomatic HIV-infected patients.
Copyright 2000 Academic Press.
Similar articles
-
Long-term clinical and surrogate marker effects of subcutaneous intermittent interleukin-2 without antiretroviral therapy in HIV-infected patients.J Antimicrob Chemother. 2008 Sep;62(3):583-6. doi: 10.1093/jac/dkn238. Epub 2008 Jun 27. J Antimicrob Chemother. 2008. PMID: 18587135 Clinical Trial.
-
Combined antiviral therapy reduces HIV-1 plasma load and improves CD4 counts but does not interfere with ongoing lymphocyte apoptosis.Immunopharmacol Immunotoxicol. 1999 Nov;21(4):645-65. doi: 10.3109/08923979909007132. Immunopharmacol Immunotoxicol. 1999. PMID: 10584202 Clinical Trial.
-
The virologic, immunologic, and clinical effects of interleukin 2 with potent antiretroviral therapy in patients with moderately advanced human immunodeficiency virus infection: a randomized controlled clinical trial--AIDS Clinical Trials Group 328.Arch Intern Med. 2007 Mar 26;167(6):597-605. doi: 10.1001/archinte.167.6.597. Arch Intern Med. 2007. PMID: 17389292 Clinical Trial.
-
[The role of therapeutic use of interleukin-2 in HIV infection].Przegl Epidemiol. 2002;56(4):587-93. Przegl Epidemiol. 2002. PMID: 12666584 Review. Polish.
-
Interleukin-2 for the treatment of human immunodeficiency virus infection.Drugs Today (Barc). 2006 Dec;42(12):791-801. doi: 10.1358/dot.2006.42.12.1025703. Drugs Today (Barc). 2006. PMID: 17285152 Review.
Cited by
-
Safety and immunologic response of a viral vaccine to prostate-specific antigen in combination with radiation therapy when metronomic-dose interleukin 2 is used as an adjuvant.Clin Cancer Res. 2008 Aug 15;14(16):5284-91. doi: 10.1158/1078-0432.CCR-07-5162. Clin Cancer Res. 2008. PMID: 18698048 Free PMC article. Clinical Trial.
-
PD-L1 blockade synergizes with IL-2 therapy in reinvigorating exhausted T cells.J Clin Invest. 2013 Jun;123(6):2604-15. doi: 10.1172/JCI67008. Epub 2013 May 15. J Clin Invest. 2013. PMID: 23676462 Free PMC article.
-
Chimeric SCID-hu Model as a Human Hematopoietic Stem Cell Host That Recapitulates the Effects of HIV-1 on Bone Marrow Progenitors in Infected Patients.J Stem Cells. 2006;1(4):283-300. J Stem Cells. 2006. PMID: 19030112 Free PMC article.
-
HIV-1 Infection-Induced Suppression of the Let-7i/IL-2 Axis Contributes to CD4(+) T Cell Death.Sci Rep. 2016 May 5;6:25341. doi: 10.1038/srep25341. Sci Rep. 2016. PMID: 27145859 Free PMC article.
-
Cellular mediators of inflammation: tregs and TH17 cells in gastrointestinal diseases.Mediators Inflamm. 2009;2009:132028. doi: 10.1155/2009/132028. Epub 2010 Feb 8. Mediators Inflamm. 2009. PMID: 20169125 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials