Le Garrec Y, Morin A
Nat Immun Cell Growth Regul. 1987;6(2):65-76.
Natural killer (NK) activity of spleen cells was studied in DBA/2 mice, 24 and 72 h after intravenous injection of various muramyl peptides: muramyl dipeptide (MDP) and derivatives which are both adjuvant-active and able to increase resistance against Klebsiella pneumoniae; derivatives which are adjuvant-active but devoid of anti-infectious properties; derivatives which are anti-infectious but devoid of adjuvant activity, and derivatives which are devoid of both activities such as the stereoisomer MDP[D-Ala]1. An early increase in NK activity was observed 24 h after injection of all nonadjuvant derivatives, whatever their effect on infection. A stimulation of natural cytotoxicity was always induced 72 h after injection of MDP and derivatives able to protect mice against Klebsiella pneumoniae infection. So, even if the reverse was not true, there seems to exist some correlation between the anti-infectious effect of muramyl peptides and the late increase in NK activity. The modulation of NK activity by muramyl peptides appeared to be independent of interferon production. Moreover, inhibition of the stimulatory effect by a cell cycle-specific drug, hydroxyurea, observed 72 h after MDP suggests a requirement for proliferation.
在给DBA/2小鼠静脉注射各种胞壁酰肽(胞壁二肽(MDP)及其衍生物,它们既有佐剂活性又能增强对肺炎克雷伯菌的抵抗力;有佐剂活性但无抗感染特性的衍生物;有抗感染特性但无佐剂活性的衍生物,以及无任何活性的衍生物如立体异构体MDP[D-Ala]1)24小时和72小时后,研究了脾细胞的自然杀伤(NK)活性。注射所有无佐剂活性的衍生物24小时后,无论它们对感染的影响如何,均观察到NK活性早期增加。注射MDP和能保护小鼠抵抗肺炎克雷伯菌感染的衍生物72小时后,总是会诱导自然细胞毒性增强。所以,即使反之不成立,但胞壁酰肽的抗感染作用与NK活性后期增加之间似乎存在某种关联。胞壁酰肽对NK活性的调节似乎与干扰素产生无关。此外,在MDP注射72小时后观察到,细胞周期特异性药物羟基脲对刺激作用有抑制,这表明需要增殖。