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B细胞源性非霍奇金淋巴瘤患者受累淋巴结中的T淋巴细胞:对恶性克隆的反应性

T lymphocytes from invaded lymph nodes in patients with B-cell-derived non-Hodgkin's lymphoma: reactivity toward the malignant clone.

作者信息

Jacob M C, Piccinni M P, Bonnefoix T, Sotto M F, Couderc P, Bensa J C, Sotto J J

机构信息

Laboratoire de recherche d'immunopathologie tumorale, hôpital A. Michallon, Grenoble, France.

出版信息

Blood. 1990 Mar 1;75(5):1154-62.

PMID:2306520
Abstract

Tumor-infiltrating T lymphocytes (TIL-T) are always present in B-cell-derived non-Hodgkin's lymphoma (NHL). In this investigation, we explored the possibility that collaboration might exist between these cells. TIL-T were isolated from 39 lymph nodes of patients with NHL. In most of the cases, few of them (less than 10%) possessed surface activation receptors CD25 or OKT9. In 80% of the cases, they proliferated in response to recombinant interleukin-2 (rIL-2), but the degree of proliferation was often low as compared with control populations. The influence of irradiated autologous malignant cells on the TIL-T proliferation in response to rIL-2 (40 U/mL) was also investigated: in 38% of the cases, this proliferation was not modified (group O), and in 41% it was higher (group +) and in 21% it was lower (group -). The mechanism of this immune response (specific or not) is not elucidated at present. The definition of these groups was statistically correlated with different parameters of the disease: (1) percentage of TIL-T was higher in group + (44% +/- 17%) than in group O (31% +/- 18%) and group - (24% +/- 15%); (2) B-cell proliferation in centrofollicular lymphomas was more frequently nodular or nodular and diffuse in group + (83%) and O (55%) than in group - (0%); (3) low-grade malignancies in the Working Formulation were more frequent in group + (75%) than in group O (60%) or group - (12%); (4) favorable prognosis evaluated with the Grenoble cytologic classification was more frequent in group + and O (87%) than in group - (12%); (5) actuarial survival curves showed a significantly better prognosis for patients in group +.

摘要

肿瘤浸润性T淋巴细胞(TIL-T)始终存在于B细胞来源的非霍奇金淋巴瘤(NHL)中。在本研究中,我们探讨了这些细胞之间可能存在协作的可能性。从39例NHL患者的淋巴结中分离出TIL-T。在大多数病例中,它们中很少(不到10%)具有表面活化受体CD25或OKT9。在80%的病例中,它们对重组白细胞介素-2(rIL-2)有增殖反应,但与对照群体相比,增殖程度通常较低。还研究了经辐照的自体恶性细胞对TIL-T在rIL-2(40 U/mL)刺激下增殖的影响:在38%的病例中,这种增殖未改变(O组),41%的病例中增殖更高(+组),21%的病例中增殖更低(-组)。目前尚不清楚这种免疫反应(是否具有特异性)的机制。这些组别的定义与疾病的不同参数在统计学上相关:(1)+组(44%±17%)的TIL-T百分比高于O组(31%±18%)和-组(24%±15%);(2)在+组(83%)和O组(55%)中,中心滤泡性淋巴瘤中的B细胞增殖比-组(0%)更频繁地呈结节状或结节状及弥漫性;(3)工作分类法中的低级别恶性肿瘤在+组(75%)中比O组(60%)或-组(12%)更常见;(4)根据格勒诺布尔细胞学分类评估的良好预后在+组和O组(87%)中比-组(12%)更常见;(5)精算生存曲线显示+组患者的预后明显更好。

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