Schuyler M R, Gott K, Shopp G, Merlin T
Department of Medicine, Albuquerque Veterans Administration Medical Center, University of New Mexico School of Medicine.
Am Rev Respir Dis. 1992 May;145(5):1185-90. doi: 10.1164/ajrccm/145.5.1185.
Experimental hypersensitivity pneumonitis (EHP) can be transferred to Strain 2 guinea pigs by peripheral lymph node (PLN) cells cultured in vitro with antigen. The phenotype of the active cells has not been delineated. In addition, it is not known if cultured lung-associated lymph node (LALN) cells can transfer EHP. PLN and LALN cells from donor animals were cultured with a soluble extract of Micropolyspora faeni (10 micrograms/ml), and blast cells were isolated by centrifugation over Percoll gradients. Cultured PLN cells were passed through nylon wool columns, and the adherent and nonadherent fractions were tested for their ability to transfer EHP. PLN blast cell populations were depleted of CD5+ cells by treatment with monoclonal anti CD5 antibody (8BE6) and complement. Syngeneic recipients received media or LALN or PLN blast cells treated with antibody plus complement, media, or complement intravenously. Recipients were challenged intratracheally with M. faeni 48 h after the cell transfer, and they were killed 4 days later. The nonadherent PLN cell population was enriched for CD5+ (T) cells and depleted of surface immunoglobulin-positive (SIg+) cells. Treatment of the PLN blast cell population with 8BE6 and complement decreased CD5+ cells from 25 to 4% and increased SIg+ cells from 62 to 80%. All animals were maintained in HEPA-filtered air. Randomly selected microscopic fields of the lung (250/animal) were judged to be normal or abnormal without knowledge of treatment. There was a low level of pulmonary response to an intratracheal challenge of M. faeni in media recipients. There was a substantial increase (p less than 0.01) of the extent of pulmonary abnormalities in the animals receiving cultured PLN cells.(ABSTRACT TRUNCATED AT 250 WORDS)
实验性过敏性肺炎(EHP)可通过体外与抗原培养的外周淋巴结(PLN)细胞转移至2号品系豚鼠。活性细胞的表型尚未明确。此外,尚不清楚培养的肺相关淋巴结(LALN)细胞是否能转移EHP。将供体动物的PLN和LALN细胞与小多孢菌可溶性提取物(10微克/毫升)一起培养,通过Percoll梯度离心分离出母细胞。培养的PLN细胞通过尼龙毛柱,测试贴壁和非贴壁部分转移EHP的能力。用单克隆抗CD5抗体(8BE6)和补体处理PLN母细胞群体,以去除CD5+细胞。同基因受体静脉注射培养基、经抗体加补体处理的LALN或PLN母细胞、培养基或补体。细胞转移48小时后,受体经气管内注射小多孢菌进行攻击,4天后处死。非贴壁PLN细胞群体富含CD5+(T)细胞,表面免疫球蛋白阳性(SIg+)细胞减少。用8BE6和补体处理PLN母细胞群体可使CD5+细胞从25%降至4%,使SIg+细胞从62%增至80%。所有动物均饲养在高效空气过滤器过滤的空气中。在不知道治疗情况的前提下,随机选择肺的显微镜视野(每只动物250个)判断为正常或异常。培养基受体对气管内注射小多孢菌的肺部反应水平较低。接受培养的PLN细胞的动物肺部异常程度大幅增加(p<0.01)。(摘要截取自250字)