Rakhmilevich A L
Trudeau Institute, Saranac Lake, New York 12983.
Immunology. 1994 Dec;83(4):524-31.
A role for alpha beta and gamma delta T cells in protection against primary and secondary infection with Listeria monocytogenes was studied. The results show that mice depleted of either gamma delta T cells with 3A10 monoclonal antibody (mAb), or alpha beta T cells with anti-CD4 plus anti-CD8 mAb, or both types of T cells, remained capable of controlling Listeria multiplication during the first 4 days of primary sublethal infection. Moreover, mice depleted of either or both types of T cells also remained capable of resolving primary infection, although the absence of alpha beta T cells, but not gamma delta T cells, caused resolution to be slower. Likewise, Listeria-immune mice depleted of either alpha beta or gamma delta T cells remained capable of resolving secondary infection with a large inoculum of L. monocytogenes, although depletion of alpha beta T cells, and to a much lesser extent gamma delta T cells, resulted in early exacerbation of infection. However, immune mice depleted of both types of T cells lost their ability to resist a lethal Listeria challenge. Taken together, the results show that whereas neither type of T cell is needed for resistance to sublethal primary listeriosis, alpha beta T cells may act in concert with gamma delta T cells in protecting mice against lethal secondary infection. In addition, the results indicate that the role of gamma delta T cells in anti-Listeria resistance is much less important than the role of alpha beta T cells, and can be demonstrated mainly in the absence of alpha beta T cells.
研究了αβ和γδ T细胞在抵御单核细胞增生李斯特菌原发性和继发性感染中的作用。结果显示,用3A10单克隆抗体(mAb)清除γδ T细胞、用抗CD4加抗CD8 mAb清除αβ T细胞或同时清除这两种类型T细胞的小鼠,在原发性亚致死感染的前4天仍能够控制李斯特菌的增殖。此外,清除一种或两种类型T细胞的小鼠也仍能够清除原发性感染,尽管缺乏αβ T细胞(而非γδ T细胞)会导致清除速度减慢。同样,清除αβ或γδ T细胞的李斯特菌免疫小鼠,在用大量单核细胞增生李斯特菌接种物进行继发性感染时仍能够清除感染,尽管清除αβ T细胞(以及在小得多的程度上清除γδ T细胞)会导致感染早期加剧。然而,清除两种类型T细胞的免疫小鼠失去了抵抗致死性李斯特菌攻击的能力。综上所述,结果表明,虽然对亚致死性原发性李斯特菌病的抵抗不需要任何一种类型的T细胞,但αβ T细胞可能与γδ T细胞协同作用,保护小鼠免受致死性继发性感染。此外,结果表明γδ T细胞在抗李斯特菌抵抗中的作用远不如αβ T细胞重要,并且主要在缺乏αβ T细胞的情况下才能显现出来。