首页> 美国卫生研究院文献>Animals : an Open Access Journal from MDPI >Clinical and Hematological Follow-Up of Long-Term Oral Therapy with Type-I Interferon in Cats Naturally Infected with Feline Leukemia Virus or Feline Immunodeficiency Virus
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Clinical and Hematological Follow-Up of Long-Term Oral Therapy with Type-I Interferon in Cats Naturally Infected with Feline Leukemia Virus or Feline Immunodeficiency Virus

机译:用猫白血病病毒或猫型免疫缺陷病毒自然感染的猫的长期口服治疗长期口服治疗的临床和血液学随访

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摘要

The viruses which produce feline leukemia (FeLV) and feline immunodeficiency (FIV) attack cells involved in the immune response. As specific drugs are either nonexistent, produce secondary effects, or are expensive, a therapeutic possibility is using nonspecific immunostimulants, such as human interferon alpha. We used this drug to treat 27 cats infected by FeLV and 31 infected by FIV. All cats were naturally infected and treatment was administered orally by their owners for four months. Participating cats were evaluated in our clinics at mid-treatment (M2), end of treatment (M4), and 4–8 months after the end of treatment (M10). We observed that treatment was well tolerated by the cats (as it did not affect the liver or the kidney functions), and improved most of the parameters analyzed (clinic, anemia, white cell counts, and CD4+/CD8+ ratio) as long as it was administered. However, 4–8 months after it was discontinued, though most animals remained clinically healthy, many of these parameters had rebounded to initial values or values even worse than the initial values. Thus, more studies should be conducted with longer administration of this drug to evaluate tolerability and sustained improvement of diseases produced by these two viruses which may lead to death.
机译:产生猫的白血病(FELV)和猫的免疫缺陷(FIV)攻击细胞的病毒参与免疫应答。由于特异性药物不存在,产生二次效果,或者是昂贵的,治疗可能性是使用非特异性免疫刺激剂,例如人干扰素α。我们使用这种药物治疗由FELV和31感染的27只猫感染。所有猫都自然感染,治疗由其业主口服给药四个月。参与猫在中期治疗(M2),治疗结束(M4)的诊所中评估了参与的猫,治疗结束后4-8个月(M10)。我们观察到猫耐受良好的治疗(因为它不影响肝脏或肾功能),并且只要它,改善了分析的大部分参数(临床,贫血,白细胞计数和CD4 + / CD8 +比率)管理。然而,在停止后4-8个月后,尽管大多数动物仍然临床健康,但许多这些参数反弹至初始值或甚至比初始值更差。因此,应使用较长施用这种药物来进行更多的研究,以评估这两种病毒产生的耐受性和持续改善可能导致死亡的病毒。

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