Chisesi T, Capnist G, Rancan L, Pellizzari G, Vespignani M
Department of Hematology, S. Bortolo Hospital, Vicenza, Italy.
J Biol Regul Homeost Agents. 1988 Oct-Dec;2(4):193-8.
Forty-one patients with Hodgkin's disease staged as IA(4), IIA/B(4/6) IIIA/B(6/9) and IVA/B(3/9) who had had radiotherapy (subtotal nodal irradiation (STNI) or total nodal irradiation (TNI), or combined one (STNI/TNI plus chemotherapy MOPP or MOPP/ABVD) have been enrolled consequently and randomized to receive thymic hormone (17 patients) or pentapeptide treatment (14 patients) for 3-6 months at the end of the therapeutic regimens. In all patients severe immunodeficiency evaluated either as leukopenia (WBC less than 4000/mm3) or lymphocytopenia (lymphocytes less than 1500/mm3) or CD3 and CD2 cell reduction, or imbalance of helper/suppressor (H/S) ratio have been documented before starting thymic therapy. Different results by immunorestorative therapy have been registered according to the entity of immunodeficiency. In fact in the group of 15 patients with severe lymphopenia (lymphocytes less than 1000/mm3) either the thymic hormone or the synthetic drug produced a significant increase of all subsets examined: CD3-CD2-CD4-CD8 without or with minimal influence on H/S ratio, due to the increase of absolute lymphocytes count. In the remaining patients with mild or no lymphopenia the two drugs resulted ineffective on T cells. Comparing the overall group of patients who received thymic therapy with a control group of patients who did not, an advantage in terms of recruitment of T cell compartment has been observed in the former group when mean values are compared. According to the clinical impact of the immunotherapy with thymic substances on these patients, a significant decrease in incidence of herpes virus infection (HVI) has been observed in patients who had had thymic therapy compared with the incidence of HVI in the control group (18% versus 53.8%).(ABSTRACT TRUNCATED AT 250 WORDS)
41例霍奇金病患者,分期为IA(4例)、IIA/B(4/6例)、IIIA/B(6/9例)和IVA/B(3/9例),接受过放疗(次全淋巴结照射(STNI)或全淋巴结照射(TNI),或两者联合(STNI/TNI加化疗MOPP或MOPP/ABVD)),随后被纳入研究并随机分组,在治疗方案结束时接受胸腺激素治疗(17例患者)或五肽治疗(14例患者),为期3 - 6个月。所有患者在开始胸腺治疗前均记录有严重免疫缺陷,表现为白细胞减少(白细胞计数低于4000/mm³)、淋巴细胞减少(淋巴细胞计数低于1500/mm³)、CD3和CD2细胞减少,或辅助/抑制(H/S)比值失衡。根据免疫缺陷的程度,免疫恢复治疗产生了不同的结果。事实上,在15例严重淋巴细胞减少(淋巴细胞计数低于1000/mm³)的患者组中,胸腺激素或合成药物使所有检测的亚群均显著增加:CD3 - CD2 - CD4 - CD8,对H/S比值无或仅有最小影响,这是由于绝对淋巴细胞计数增加。在其余轻度或无淋巴细胞减少的患者中,这两种药物对T细胞无效。将接受胸腺治疗的患者总体组与未接受治疗的对照组进行比较,当比较平均值时,在前一组中观察到T细胞区室募集方面的优势。根据胸腺物质免疫治疗对这些患者的临床影响,与对照组相比,接受胸腺治疗的患者中疱疹病毒感染(HVI)的发生率显著降低(18%对53.8%)。(摘要截短于250字)