Eckels D D, Sell T W, Bronson S R, Johnson A H, Hartzman R J, Lamb J R
Immunogenetics. 1984;19(5):409-23. doi: 10.1007/BF00364644.
Human T-lymphocyte clones ( TLCs ) were generated against the hemagglutinin (HA) of A/Texas/1/77 influenza virus by limiting dilution. TLCs were then screened for antigen specificity on chemically synthesized peptides representing the HA1 molecule. It has been hypothesized that different T cells that recognize the identical antigenic determinant are controlled by (restricted by) the same class II epitope. Two TLCs , HA1.4 and HA1.7, both recognized the same HA peptide and in proliferation studies exhibited identical restriction patterns. Two other clones, HA 1.9 and HA 2.43, recognized different HA determinants and also had distinct restriction patterns. Proliferation inhibition studies with monoclonal antibodies against human class II molecules demonstrated three unique patterns of blocking with the clones, suggesting that clones may be restricted to a unique class II epitope depending on the HA determinant recognized. These data can be interpreted as supporting the argument that human immune responses to influenza hemagglutinin are under Ir gene control exerted at the level of the viral antigenic determinant recognized in association with particular D-region restricting elements. The determinant selection and clonal deletion theories are compared for their capacity to best explain these findings.
通过有限稀释法产生了针对A/德克萨斯/1/77流感病毒血凝素(HA)的人T淋巴细胞克隆(TLC)。然后在代表HA1分子的化学合成肽上筛选TLC的抗原特异性。据推测,识别相同抗原决定簇的不同T细胞受(受限于)相同的II类表位控制。两个TLC,HA1.4和HA1.7,都识别相同的HA肽,并且在增殖研究中表现出相同的限制模式。另外两个克隆,HA 1.9和HA 2.43,识别不同的HA决定簇,并且也有不同的限制模式。用针对人II类分子的单克隆抗体进行的增殖抑制研究表明,这些克隆有三种独特的阻断模式,这表明根据所识别的HA决定簇,克隆可能受限于独特的II类表位。这些数据可以解释为支持这样的观点,即人类对流感血凝素的免疫反应受Ir基因控制,这种控制在与特定D区限制元件相关联所识别的病毒抗原决定簇水平上发挥作用。比较了决定簇选择和克隆缺失理论对这些发现的最佳解释能力。