Kuni-Eda Y, Okabe M, Kurosawa M, Maekawa I, Higuchi M, Kawamura M, Morioka M, Suzuki S, Ohmura T, Fujimoto N
Third Department of Internal Medicine, Hokkaido University School of Medicine, Sapporo, Japan.
Leuk Lymphoma. 1995 Feb;16(5-6):471-6. doi: 10.3109/10428199509054436.
It has been previously demonstrated that the administration of recombinant human granulocyte-colony stimulating factor (rhG-CSF) ameliorates the decrease of the polymorphonuclear neutrophils (PMNs) count after the cytotoxic chemotherapies, thereby reducing the infection complications associated with neutropenia. In this multi-center study, we studied the prophylaxtic effect of rhG-CSF administration on infection complications in patients with non-Hodgkin malignant lymphoma, who received cytotoxic chemotherapies (CHOP or ProMACE/CytaBOM). rhG-CSF administration reduced the frequency of infection complications, and there was no obvious difference in it's frequency between the CHOP-treated and the ProMACE/CytaBOM-treated groups when administered with rhG-CSF, thereby indicating that third generation therapy for NHL may be safely completed in Japanese in combination with rhG-CSF administration. Furthermore, we investigated both the in vitro and the in vivo effects of rhG-CSF on the function of PMNs in patients with NHL and healthy donors, and revealed that the administration of rhG-CSF for NHL patients receiving cytotoxic chemotherapy brought on an improvement of the production of active oxygen but did not affect serum levels of IFNs, IL-1-beta, and IL-6, inspite of a slight elevation of TNF-alpha. Consistent with these results, in vitro treatment of PMNs with rhG-CSF induced no significant production of these inflammatory cytokines and their mRNA expressions. Furthermore, rhG-CSF administration showed no significant effects in vivo on the expression of CD11a, CD11b and LECAM-1 on PMNs and integrins on platelets.
先前已证明,给予重组人粒细胞集落刺激因子(rhG-CSF)可改善细胞毒性化疗后多形核中性粒细胞(PMN)计数的下降,从而减少与中性粒细胞减少相关的感染并发症。在这项多中心研究中,我们研究了给予rhG-CSF对接受细胞毒性化疗(CHOP或ProMACE/CytaBOM)的非霍奇金恶性淋巴瘤患者感染并发症的预防作用。给予rhG-CSF可降低感染并发症的发生率,在给予rhG-CSF时,CHOP治疗组和ProMACE/CytaBOM治疗组之间的发生率无明显差异,这表明在日本,非霍奇金淋巴瘤的第三代治疗联合给予rhG-CSF可能安全完成。此外,我们研究了rhG-CSF对非霍奇金淋巴瘤患者和健康供体中PMN功能的体外和体内效应,发现给予接受细胞毒性化疗的非霍奇金淋巴瘤患者rhG-CSF可改善活性氧的产生,但尽管肿瘤坏死因子-α略有升高,但对干扰素、白细胞介素-1β和白细胞介素-6的血清水平无影响。与这些结果一致,用rhG-CSF体外处理PMN不会诱导这些炎性细胞因子的显著产生及其mRNA表达。此外,给予rhG-CSF在体内对PMN上的CD11a、CD11b和LECAM-1以及血小板上的整合素的表达无显著影响。