We have investigated the effects of combination therapy with thymosin alpha1 and natural human lymphoblastoid interferon-alpha in human immunodeficiency virus infection and have shown that in vitro this combination treatment: (1) synergistically stimulated the cytotoxic activity against natural killer-sensitive target cells of lymphocytes collected from human immunodeficiency virus-infected donors and (2) did not interfere with the antiviral activity of zidovudine. We thus studied the effects of combination therapy with thymosin alpha1, interferon-alpha and zidovudine in patients with CD4+ lymphocytes ranging from 200 to 500/mm3 in a randomized non-blinded study and found that the treatment was well tolerated after 12 months of therapy and was associated with a substantial increase in the number and function of CD4+ T cells. A similar effect was not observed in human immunodeficiency virus patients treated with zidovudine alone or associated with single agents. These data suggest the need for a controlled, double-blind clinical trial, recently initiated with the approval and the support of the Italian Ministry of Health.

Garaci, E., Rocchi, G., Perroni, L., D'Agostini, C., Soscia, F., Grelli, S., et al. (1994). Combination treatment with zidovudine, thymosin alpha 1 and interferon-alpha in human immunodeficiency virus infection. INTERNATIONAL JOURNAL OF CLINICAL & LABORATORY RESEARCH, 24(1), 23-28.

Combination treatment with zidovudine, thymosin alpha 1 and interferon-alpha in human immunodeficiency virus infection.

GARACI, ENRICO;ROCCHI, GIOVANNI;GRELLI, SANDRO;FAVALLI, CARTESIO
1994-01-01

Abstract

We have investigated the effects of combination therapy with thymosin alpha1 and natural human lymphoblastoid interferon-alpha in human immunodeficiency virus infection and have shown that in vitro this combination treatment: (1) synergistically stimulated the cytotoxic activity against natural killer-sensitive target cells of lymphocytes collected from human immunodeficiency virus-infected donors and (2) did not interfere with the antiviral activity of zidovudine. We thus studied the effects of combination therapy with thymosin alpha1, interferon-alpha and zidovudine in patients with CD4+ lymphocytes ranging from 200 to 500/mm3 in a randomized non-blinded study and found that the treatment was well tolerated after 12 months of therapy and was associated with a substantial increase in the number and function of CD4+ T cells. A similar effect was not observed in human immunodeficiency virus patients treated with zidovudine alone or associated with single agents. These data suggest the need for a controlled, double-blind clinical trial, recently initiated with the approval and the support of the Italian Ministry of Health.
1994
Pubblicato
Rilevanza internazionale
Articolo
Sì, ma tipo non specificato
Settore MED/07 - MICROBIOLOGIA E MICROBIOLOGIA CLINICA
English
Con Impact Factor ISI
alpha interferon; biological response modifier; drug derivative; thymosin; thymosin alpha1; zidovudine; adult; article; CD4+ T lymphocyte; clinical trial; comparative study; controlled clinical trial; controlled study; cytotoxicity; drug effect; drug potentiation; female; human; Human immunodeficiency virus; Human immunodeficiency virus infection; leukocyte count; male; multimodality cancer therapy; physiology; randomized controlled trial; risk factor; virus replication; Adult; Biological Response Modifiers; CD4-Positive T-Lymphocytes; Combined Modality Therapy; Cytotoxicity, Immunologic; Drug Synergism; Female; HIV; HIV Infections; Humans; Interferon-alpha; Leukocyte Count; Male; Risk Factors; Thymosin; Virus Replication; Zidovudine
Garaci, E., Rocchi, G., Perroni, L., D'Agostini, C., Soscia, F., Grelli, S., et al. (1994). Combination treatment with zidovudine, thymosin alpha 1 and interferon-alpha in human immunodeficiency virus infection. INTERNATIONAL JOURNAL OF CLINICAL & LABORATORY RESEARCH, 24(1), 23-28.
Garaci, E; Rocchi, G; Perroni, L; D'Agostini, C; Soscia, F; Grelli, S; Mastino, A; Favalli, C
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/52003
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