Abstract

The aim of the study was to determine the efficacy of recombinant human interferon lambda 1 (IFN-λ1) against human adenovirus serotype 5 in a culture of human conjunctival cells Chang conjunctiva clone 1-5c-4. Material and methods. The study design consisted of three experimental schemes, reflecting a prophylactic and two options for a therapeutic and prophylactic treatment regimen (with the constant presence of the virus in the culture medium and with its removal after adsorption). The antiviral activity of IFN-λ1 was determined by the number of viable cells after exposure to the virus (MTT test). Results and discussion. It has been established that IFN-λ1 has antiviral activity against human adenovirus in vitro under a prophylactic and therapeutic-prophylactic scheme of administration at an infection dose of 1 and 10 TCID50 (50% tissue culture infectious dose), but not at an infection dose of 100 TCID50. The antiviral effect of the use of IFN-λ1 in a therapeutic and prophylactic regimen at an infection dose of 1 TCID50 was comparable to that of IFN-α. At the same time, both interferons did not have a toxic effect on the cell culture even at a concentration of 84 and 58 μg/ml, respectively. The antiviral activity and the absence of cytotoxic action provide the basis for further study of the possibility of development of based on IFN-λ1 drug for eye conjunctiva viral diseases treatment.

Highlights

  • The aim of the study was to determine the efficacy of recombinant human interferon lambda 1

  • The study design consisted of three experimental schemes

  • The antiviral activity of IFN-λ1 was determined by the number of viable cells

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Summary

Introduction

Цель настоящего исследования – изучение противовирусной активности рекомбинантного человеческого ИФН-λ1 в отношении аденовируса человека серотипа 5 in vitro на культуре клеток конъюнктивы человека Chang conjunctiva clone 1-5c-4. Через 30 мин после заражения клеток в лунки вновь вносили исследуемый образец (разведения от 1:10 до 1:2560) в 100 мкл поддерживающей среды и инкубировали при 37 °C в атмосфере с 5 % СО2 в течение 72 ч.

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