Cottagnoud P, Neftel K A, Hany M, Zinkernagel R M
Institute of Pathology, University Hospital, Zürich, Switzerland.
Antiviral Res. 1988 Nov;10(1-3):59-70. doi: 10.1016/0166-3542(88)90014-9.
Derivatives of beta-lactam antibiotics of the cephalosporin type at 0.02-1 mM concentrations interfered with in vitro replication of two DNA-containing viruses, herpes simplex I and vaccinia, but showed no effects on two RNA-viruses, lymphocytic choriomeningitis virus and vesicular stomatitis virus, or on cell viability. The exact structure of the active compounds remains unknown, but opening of the beta-lactam ring appears to be a prerequisite for their formation. Whereas cephalosporin derivatives were most active, no active products were obtained from penicillins and monobactams. The potential of these unexpected antiviral effects of widely used beta-lactam antibiotics remains subject of further study.
头孢菌素类β-内酰胺抗生素的衍生物在浓度为0.02-1 mM时,会干扰两种含DNA病毒——单纯疱疹病毒I型和痘苗病毒的体外复制,但对两种RNA病毒——淋巴细胞性脉络丛脑膜炎病毒和水疱性口炎病毒,或对细胞活力没有影响。活性化合物的确切结构仍然未知,但β-内酰胺环的打开似乎是其形成的先决条件。虽然头孢菌素衍生物活性最强,但青霉素和单环β-内酰胺未得到活性产物。这些广泛使用的β-内酰胺抗生素意外的抗病毒作用的潜力仍有待进一步研究。