The impact of antibodies to human glycoprotein CD4 and gamma-interferon on the t-cell immunity and the cytokine levels in patients co-infected with HIV/HCV during the antiretroviral therapy
Objective: This work was to estimate the influence of antibodies to human glycoprotein CD4 and IFN-γ on the T-cell immunity and the cytokine levels in patients with HIV and HIV/HCV during the standard antiretroviral therapy. Materials and methods: Randomized clinical trial in parallel groups. 4 grou...
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| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
State Budget Educational Institute of Higher Professional Education, Rostov State Medical University, Ministry Health of Russian Federation
2017-06-01
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| Series: | Медицинский вестник Юга России |
| Subjects: | |
| Online Access: | https://www.medicalherald.ru/jour/article/view/550 |
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| Summary: | Objective: This work was to estimate the influence of antibodies to human glycoprotein CD4 and IFN-γ on the T-cell immunity and the cytokine levels in patients with HIV and HIV/HCV during the standard antiretroviral therapy. Materials and methods: Randomized clinical trial in parallel groups. 4 groups were included: patients with HIV receiving ART (20) or ART and antibodies (AB) (19) for 3 months; patients with HIV/HCV, receiving ART (17) or ART and AB (20) for 3 months. The obtained data included: CD3+, CD4+, CD8+ cell count; IFN-γ, IL-2 and IL-4 concentrations; HIV viral load. Results: The significant increase of CD4+ cell number and IFN-γ were found in patients receiving ART and antibodies. These changes were followed with more significant decline in the viral load. Conclusion: The antibodies to human glycoprotein CD4 and IFN-γ added to standard ART increased the CD4+ cell count and IFN-γ levels in patients with HIV/HCV, followed by the trend to increase the number of patients with viral load >50 ml-1. Thus, the administration of ART supplemented with antibodies to human glycoprotein CD4 and IFN-γ resulted in the increase of antiviral immunity. Further clinical trials in HIV or HIV patients with co-infections could be recommended. |
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| ISSN: | 2219-8075 2618-7876 |