Immuno-activation with anti-CD3 and recombinant human IL-2 in HIV-1-infected patients on potent antiretroviral therapy

Autor: C. H. Fox, Hetty Blaak, van R.P. Rij, de F. Wolf, J. M. A. Lange, Hanneke Schuitemaker, van R.M.E. Praag, ten R.J.M. Berge, Suzanne Jurriaans, P. T. A. Schellekens, Marijke T. L. Roos, Jaap Goudsmit, S.L. Yong, Jan M. Prins
Přispěvatelé: Other departments
Jazyk: angličtina
Rok vydání: 1999
Předmět:
Zdroj: AIDS (London, England), 13(17), 2405-2410. Lippincott Williams and Wilkins
ISSN: 0269-9370
DOI: 10.1097/00002030-199912030-00012
Popis: Background A stable reservoir of latently infected, resting CD4 T cells has been demonstrated in HIV-1-infected patients despite prolonged antiretroviral treatment. This is a major barrier for the eradication of HIV by antiretroviral agents alone. Activation of these cells in the presence of antiretroviral therapy might be a strategy to increase the turnover rate of this reservoir. Methods Three HIV-1-positive patients on potent antiretroviral therapy, in whom plasma viremia had been suppressed to below 5 copies/ml for at least 26 weeks, were treated with a combination of OKT3 (days 1-5) and recombinant human IL-2 (days 2 6). Results The side-effects were fever, headache, nausea, diarrhea, and in one of the patients transient renal failure and seizures. The regimen resulted in profound T cell activation. In one patient plasma HIV-1 RNA transiently increased with a peak at 1500 copies/ml. In the other two patients plasma HIV-1 RNA levels remained below the detection limit, but HIV-1 RNA levels in the lymph nodes increased two- to threefold. All patients developed antibodies against OKT3. Conclusion OKT3/IL-2 resulted in T cell activation and proliferation, and could stimulate HIV replication in patients having achieved prolonged suppression of plasma viremia. OKT3/IL-2 therapy was toxic and rapidly induced antibodies against OKT3.
Databáze: OpenAIRE