Kearns R J, DeFreitas E C
Infect Immun. 1983 May;40(2):713-9. doi: 10.1128/iai.40.2.713-719.1983.
Murine T cells generated against heat-killed Listeria monocytogenes or Listeria intracellular product (LIP) were propagated in a source of Interleukin 2. Both T-cell cultures were greater than 98% Lyt 1+, 2/3- and proliferated specifically against LIP and L. monocytogenes crude whole-cell antigen in vitro. Proliferation of both T-cell cultures required the presence of antigen and accessory cells syngeneic to the T cells at the left end of the major histocompatibility complex. The ability of these cultures to adoptively transfer protection against challenge with viable Listeria cells was dramatically different. As few as 10(6) LIP-specific T cells conferred significant protection against a lethal challenge of Listeria cells, whereas cultures induced against crude whole-cell antigen showed little or no protective function. The resistance conferred by LIP-specific T cells was specific in that the cells did not reduce the mortality seen after challenge with Salmonella typhimurium.
针对热灭活单核细胞增生李斯特菌或李斯特菌胞内产物(LIP)产生的小鼠T细胞在白细胞介素2来源中进行增殖。两种T细胞培养物中Lyt 1 +、2/3 -细胞均超过98%,并且在体外针对LIP和单核细胞增生李斯特菌粗全细胞抗原进行特异性增殖。两种T细胞培养物的增殖都需要抗原以及主要组织相容性复合体左端与T细胞同基因的辅助细胞的存在。这些培养物过继转移针对活李斯特菌细胞攻击的保护能力存在显著差异。低至10(6)个LIP特异性T细胞就能对李斯特菌细胞的致死性攻击提供显著保护,而针对粗全细胞抗原诱导产生的培养物则几乎没有或完全没有保护功能。LIP特异性T细胞赋予的抗性具有特异性,因为这些细胞不会降低鼠伤寒沙门氏菌攻击后出现的死亡率。