Matsuzaki G, Vordermeier H M, Hashimoto A, Nomoto K, Ivanyi J
MRC Clinical Sciences Centre, Hammersmith Hospital, London, W12 0NN, United Kingdom.
Cell Immunol. 1999 Jun 15;194(2):178-85. doi: 10.1006/cimm.1999.1503.
To clarify the role of B cells in the establishment of T cell response against intracellular bacteria, B-cell-deficient (muMT-/-) mice were infected with an intracellular bacteria, Listeria monocytogenes, and T cell response against the bacteria was analyzed. On day 6 of primary Listeria infection, spleen T cells of the muMT-/- mice showed significantly lower levels of proliferative response and IFN-gamma production than those of normal infected mice after in vitro stimulation with listerial antigen. Even in the secondary Listeria infection after immunization with viable bacteria, spleen T cells of the muMT-/- mice proliferated and produced IFN-gamma against listerial antigen at significantly lower levels than those of normal immunized mice. These results demonstrate participation of B cells in priming of Listeria-specific T cells in vivo. However, B cells failed to present Listeria antigen to Listeria-specific T cells in vitro unless Listeria antigen was solubilized. Furthermore, transfer of immune serum from Listeria-infected normal mice failed to enhance the Listeria-specific T cell response of muMT-/- mice. The results indicate that B cells support the T cell response against intracellular bacteria through a mechanism other than their Ig production or antigen presentation function.
为阐明B细胞在针对细胞内细菌的T细胞应答建立过程中的作用,用细胞内细菌单核细胞增生李斯特菌感染B细胞缺陷(muMT-/-)小鼠,并分析针对该细菌的T细胞应答。在原发性李斯特菌感染的第6天,用李斯特菌抗原体外刺激后,muMT-/-小鼠的脾脏T细胞增殖反应水平和IFN-γ产生量显著低于正常感染小鼠。即使在用活细菌免疫后的继发性李斯特菌感染中,muMT-/-小鼠的脾脏T细胞针对李斯特菌抗原的增殖和IFN-γ产生水平也显著低于正常免疫小鼠。这些结果表明B细胞参与了体内李斯特菌特异性T细胞的启动。然而,除非李斯特菌抗原被溶解,否则B细胞在体外无法将李斯特菌抗原呈递给李斯特菌特异性T细胞。此外,将来自李斯特菌感染的正常小鼠的免疫血清转移给muMT-/-小鼠,未能增强其李斯特菌特异性T细胞应答。结果表明,B细胞通过其抗体产生或抗原呈递功能以外的机制支持针对细胞内细菌的T细胞应答。