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造血生长因子作为抗逆转录病毒疗法的辅助治疗手段。

Hematopoietic growth factors as adjuncts to antiretroviral therapy.

作者信息

Miles S A

机构信息

Division of Hematology-Oncology, UCLA School of Medicine.

出版信息

AIDS Res Hum Retroviruses. 1992 Jun;8(6):1073-80. doi: 10.1089/aid.1992.8.1073.

Abstract

Anemia and neutropenia are common complications of HIV infection. Antiretroviral therapy with zidovudine exacerbates bone marrow suppression by inhibiting proliferation of blood cell progenitor cells. In addition, treatment for opportunistic infections or malignancies can involve the use of myelosuppressive drugs. As a consequence, severe anemia and neutropenia can result, thereby limiting the utilization of antiretroviral drugs. Since antiretroviral therapy can increase survival, drugs that ameliorate myelosuppression are important adjuncts in the treatment of HIV-infected patients. Three hematopoietic growth factors are effective in the treatment of anemia or neutropenia. In four placebo-controlled trials, erythropoietin (EPO) at doses up to 600 U/kg/wk decreased mean transfusion requirements by 37%, increased mean hematocrit by 4.5% and corrected anemia in the majority of patients receiving zidovudine over a 12-week period. In a separate study, granulocyte colony-stimulating factor (G-CSF) corrected leukopenia and isolated neutrophil defects in 22 patients with AIDS without altering HIV expression. When erythropoietin was added to the regimen, combined G-CSF and EPO corrected both anemia and leukopenia and lessened subsequent zidovudine toxicity. Similarly, granulocyte macrophage-colony-stimulating factor (GM-CSF) corrected leukopenia and pre-existing neutrophil defects in patients with HIV infection. In controlled and uncontrolled trials, GM-CSF also appears to reduce toxicity from zidovudine, ganciclovir, and antineoplastic therapy. New combinations of hematopoietic stimulants are being used to decrease the toxicity from combination antiretroviral therapy with alpha interferon and cytotoxic chemotherapy in the treatment of AIDS-related malignancies.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

贫血和中性粒细胞减少是HIV感染的常见并发症。齐多夫定抗逆转录病毒疗法通过抑制血细胞祖细胞的增殖加剧骨髓抑制。此外,机会性感染或恶性肿瘤的治疗可能涉及使用骨髓抑制药物。因此,可能导致严重贫血和中性粒细胞减少,从而限制抗逆转录病毒药物的使用。由于抗逆转录病毒疗法可提高生存率,改善骨髓抑制的药物是治疗HIV感染患者的重要辅助药物。三种造血生长因子对贫血或中性粒细胞减少的治疗有效。在四项安慰剂对照试验中,剂量高达600 U/kg/周的促红细胞生成素(EPO)在12周内使接受齐多夫定治疗的大多数患者的平均输血需求降低了37%,平均血细胞比容提高了4.5%,并纠正了贫血。在另一项研究中,粒细胞集落刺激因子(G-CSF)纠正了22例艾滋病患者的白细胞减少和孤立性中性粒细胞缺陷,而未改变HIV表达。当促红细胞生成素添加到治疗方案中时,联合使用G-CSF和EPO可同时纠正贫血和白细胞减少,并减轻随后的齐多夫定毒性。同样,粒细胞巨噬细胞集落刺激因子(GM-CSF)纠正了HIV感染患者的白细胞减少和既往存在的中性粒细胞缺陷。在对照和非对照试验中,GM-CSF似乎也能降低齐多夫定、更昔洛韦和抗肿瘤治疗的毒性。造血刺激剂的新组合正被用于降低在治疗艾滋病相关恶性肿瘤时联合使用α干扰素和细胞毒性化疗的抗逆转录病毒疗法的毒性。(摘要截取自250字)

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