Tricerri A, Guidi L, Frasca D, Costanzo M, Errani A R, Riccioni M E, Barattini P, Vangeli M, Bartoloni C, Coppola R, Doria G, Gasbarrini G
Institute of Internal and Geriatric Medicine, Università Cattolica del Sacro Cuore, and Laboratory of Immunology, ENEA-CRE, Casaccia, Rome, Italy.
Scand J Gastroenterol. 1999 Aug;34(8):757-64. doi: 10.1080/003655299750025679.
Between peripheral blood and tissue-infiltrating lymphocytes there is an intermediate compartment, the blood of the organ-draining vessels, which could show unusual features. The aim of the present study was to analyse the characteristics of the lymphocytes from the stomach-draining vessels and the cytokine secretion by these lymphocytes. The CagA-mediated lymphocyte activation in Helicobacter pylori-infected subjects and the humoral response to this antigen were evaluated and correlated with clinical data.
We studied lymphocyte proliferation either with mitogens or with the CagA antigen and cytokine production and IgG anti-CagA by means of an enzyme-linked immunosorbent assay in peripheral blood and gastric-vein blood obtained during surgical intervention.
We showed higher proliferative response and cytokine production in lymphocytes from the gastric vein. The mitogenic response to the CagA antigen was highly specific but poorly sensitive for the H. pylori infection in both the compartments. The overall cytokine profile in our patients affected by non-ulcer disease was of the Th0 type.
Gastric-vein-derived lymphocytes seem to show unusual features, as they behave like peripheral blood lymphocytes but show higher responses to all the tested stimuli. It is possible that the interaction of the lymphocytes with the mucosal environment could activate the synthetic mechanisms, making the cells more 'responsive' to the stimulation. The CagA antigen is able to induce a specific T-lymphocyte response and is therefore a valid candidate antigen for the development of a vaccine.
在外周血和组织浸润淋巴细胞之间存在一个中间区室,即器官引流血管的血液,其可能呈现出不同寻常的特征。本研究旨在分析胃引流血管淋巴细胞的特征以及这些淋巴细胞的细胞因子分泌情况。还评估了幽门螺杆菌感染受试者中CagA介导的淋巴细胞活化以及对该抗原的体液反应,并将其与临床数据相关联。
我们通过在手术干预期间采集的外周血和胃静脉血中进行酶联免疫吸附测定,研究了淋巴细胞对有丝分裂原或CagA抗原的增殖情况、细胞因子产生以及抗CagA IgG情况。
我们发现胃静脉淋巴细胞具有更高的增殖反应和细胞因子产生。对CagA抗原的有丝分裂原反应在两个区室中对幽门螺杆菌感染都具有高度特异性但敏感性较差。我们的非溃疡疾病患者的总体细胞因子谱属于Th0型。
胃静脉来源的淋巴细胞似乎呈现出不同寻常的特征,因为它们的行为类似于外周血淋巴细胞,但对所有测试刺激均表现出更高的反应。淋巴细胞与黏膜环境的相互作用可能激活合成机制,使细胞对刺激更“敏感”。CagA抗原能够诱导特异性T淋巴细胞反应,因此是开发疫苗的有效候选抗原。